580 Psychology Research jobs in India
Senior Research Scientist - Educational Psychology
500001 Shaikpet, Andhra Pradesh
₹1600000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
Our client, a pioneering educational research institution, is seeking a Senior Research Scientist specializing in Educational Psychology. This is a challenging and rewarding role for an individual with a strong academic background and a proven track record in designing and conducting research to improve learning outcomes and educational practices. The scientist will lead research projects, analyze data, and disseminate findings to contribute to the advancement of educational theory and application.
Key responsibilities include developing research proposals, designing studies, and overseeing data collection processes. You will conduct advanced statistical analyses of qualitative and quantitative data, interpreting findings within the context of educational psychology. The role involves collaborating with educators, policymakers, and other researchers to translate research insights into practical, evidence-based interventions and recommendations. You will also be responsible for writing grant proposals, publishing research in peer-reviewed journals, and presenting findings at academic conferences. Mentoring junior researchers and contributing to the strategic direction of the research department will be integral parts of the job.
This position is based at our client's state-of-the-art research facility in **Hyderabad, Telangana, IN**. While some research activities might involve remote data analysis, the core of this role requires active participation in on-site research, laboratory work, and collaborative meetings. The ideal candidate possesses exceptional analytical skills, a deep understanding of research methodologies in education, and a passion for making a tangible impact on the learning landscape.
Qualifications:
Key responsibilities include developing research proposals, designing studies, and overseeing data collection processes. You will conduct advanced statistical analyses of qualitative and quantitative data, interpreting findings within the context of educational psychology. The role involves collaborating with educators, policymakers, and other researchers to translate research insights into practical, evidence-based interventions and recommendations. You will also be responsible for writing grant proposals, publishing research in peer-reviewed journals, and presenting findings at academic conferences. Mentoring junior researchers and contributing to the strategic direction of the research department will be integral parts of the job.
This position is based at our client's state-of-the-art research facility in **Hyderabad, Telangana, IN**. While some research activities might involve remote data analysis, the core of this role requires active participation in on-site research, laboratory work, and collaborative meetings. The ideal candidate possesses exceptional analytical skills, a deep understanding of research methodologies in education, and a passion for making a tangible impact on the learning landscape.
Qualifications:
- Ph.D. in Educational Psychology, Psychology, or a related field with a strong research focus.
- Minimum of 7 years of post-doctoral research experience in educational settings.
- Demonstrated expertise in designing and implementing quantitative and qualitative research methodologies.
- Advanced proficiency in statistical analysis software (e.g., SPSS, R, Stata) and data visualization techniques.
- Proven experience in securing research funding through grant writing.
- Excellent scientific writing and presentation skills, with a strong publication record.
- Experience in mentoring junior researchers or graduate students.
- Strong collaborative and interpersonal skills for effective teamwork.
This advertiser has chosen not to accept applicants from your region.
0
Principal Research Fellow, Educational Psychology
800001 Patna, Bihar
₹75000 Annually
WhatJobs
Posted 13 days ago
Job Viewed
Job Description
Our client, a leading research university committed to advancing educational practices, is seeking a highly accomplished Principal Research Fellow in Educational Psychology to join their esteemed faculty. This hybrid role, based in Patna, Bihar, IN , offers a dynamic blend of on-campus collaboration and remote research flexibility. The Principal Research Fellow will lead significant research projects focused on understanding and improving learning processes, student motivation, and pedagogical effectiveness across diverse educational settings.
Key Responsibilities:
Key Responsibilities:
- Design, conduct, and manage high-impact research studies in educational psychology, adhering to rigorous academic standards.
- Investigate critical areas such as cognitive development, learning strategies, socio-emotional learning, and the impact of educational interventions.
- Secure external research funding through grant writing and proposal development.
- Analyze quantitative and qualitative research data using appropriate statistical and analytical methodologies.
- Publish research findings in leading peer-reviewed academic journals and present at national and international conferences.
- Supervise and mentor graduate students and junior researchers involved in research projects.
- Collaborate with faculty members, educational institutions, and community partners to translate research into practical educational applications.
- Contribute to the development of curriculum and teaching materials related to educational psychology.
- Stay abreast of the latest research trends and theoretical advancements in the field.
- Manage research budgets and project timelines efficiently.
- Contribute to the broader academic and research community within the university.
- Ph.D. in Educational Psychology, Developmental Psychology, or a closely related field.
- Minimum of 7 years of post-doctoral research experience, with a strong publication record in reputable academic journals.
- Demonstrated success in securing research grants from national or international funding bodies.
- Expertise in research design, statistical analysis (e.g., regression, ANOVA, SEM), and qualitative research methods.
- Proven ability to lead research teams and mentor junior academics.
- Excellent written and verbal communication skills, with the ability to articulate complex research findings effectively.
- A deep understanding of learning theories, motivation, and child development.
- Experience in collaborating with K-12 schools or higher education institutions is highly desirable.
- Proficiency in statistical software packages such as SPSS, R, or Stata.
- A passion for contributing to the improvement of education through evidence-based research.
This advertiser has chosen not to accept applicants from your region.
1
Postdoctoral Research Fellow - Educational Psychology
380001 Ahmedabad, Gujarat
₹700000 Annually
WhatJobs
Posted 16 days ago
Job Viewed
Job Description
Our client, a prestigious research university renowned for its cutting-edge studies in education, is seeking a highly motivated and accomplished Postdoctoral Research Fellow to join their esteemed faculty on a fully remote basis. This is an exceptional opportunity for an individual passionate about educational psychology to contribute to significant research projects, publish scholarly work, and advance their academic career in a dynamic, virtual environment. You will collaborate with leading researchers and engage in innovative pedagogical investigations.
Responsibilities:
Qualifications:
This is an exciting opportunity to contribute to pioneering research from anywhere, with primary project coordination linked to **Ahmedabad, Gujarat, IN**.
Responsibilities:
- Conduct independent and collaborative research in the field of educational psychology, focusing on areas such as learning, motivation, cognitive development, and educational interventions.
- Design, implement, and analyze research studies using a variety of quantitative and qualitative methodologies.
- Collect and analyze research data using statistical software (e.g., SPSS, R, STATA) and qualitative analysis tools.
- Prepare manuscripts for publication in high-impact peer-reviewed journals.
- Present research findings at national and international academic conferences.
- Contribute to grant writing and the acquisition of research funding.
- Mentor graduate and undergraduate students involved in research projects.
- Assist in the development and refinement of research protocols and ethical review board applications.
- Stay abreast of the latest developments and theoretical advancements in educational psychology and related fields.
- Collaborate with faculty and researchers across departments and institutions.
- Contribute to the overall research output and reputation of the department.
- Manage research projects, including timelines, budgets, and data integrity.
- Assist in the development of new research initiatives and research proposals.
- Participate in departmental seminars and academic discussions.
- Maintain accurate and organized research records and documentation.
Qualifications:
- Ph.D. in Educational Psychology, Psychology, Education, or a closely related field.
- Demonstrated record of high-quality research output, including publications in reputable academic journals.
- Strong theoretical knowledge and practical experience in research design, data collection, and analysis relevant to educational psychology.
- Proficiency in statistical analysis software (e.g., SPSS, R) and/or qualitative data analysis software.
- Excellent written and verbal communication skills, with the ability to articulate complex research findings clearly and effectively.
- Ability to work independently, manage research projects autonomously, and meet deadlines in a remote setting.
- Strong analytical and critical thinking skills.
- Experience with grant writing is highly desirable.
- Ability to collaborate effectively with a diverse group of researchers and students.
- A passion for advancing knowledge in educational psychology.
- Experience mentoring students is an advantage.
- Familiarity with learning management systems (LMS) and online educational platforms is beneficial.
This is an exciting opportunity to contribute to pioneering research from anywhere, with primary project coordination linked to **Ahmedabad, Gujarat, IN**.
This advertiser has chosen not to accept applicants from your region.
2
Lead Research Scientist - Educational Psychology
208001 Kanpur, Uttar Pradesh
₹1000000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client is seeking a visionary Lead Research Scientist specializing in Educational Psychology to spearhead innovative research initiatives. This fully remote position allows you to contribute your expertise to advancing learning sciences and developing evidence-based educational interventions from anywhere. The ideal candidate will have a deep understanding of cognitive development, learning theories, and educational assessment, coupled with a strong record of conducting rigorous academic research. You will be responsible for designing and leading research projects, analyzing complex datasets, interpreting findings, and translating them into actionable insights for curriculum development and pedagogical strategies. This role involves collaborating with a diverse team of researchers, educators, and data scientists, publishing in peer-reviewed journals, and presenting research at leading academic conferences. A Ph.D. in Educational Psychology or a closely related field is essential, along with proven experience in grant writing and project management.
Key Responsibilities:
Qualifications:
This is a unique opportunity to make a significant contribution to the field of education research and drive meaningful change. Our client offers a competitive salary, excellent benefits, and the flexibility of a fully remote work environment.
Key Responsibilities:
- Design and direct large-scale research projects focused on learning, cognition, and educational outcomes.
- Develop research methodologies, including experimental, quasi-experimental, and correlational designs.
- Analyze quantitative and qualitative data using advanced statistical techniques.
- Interpret research findings and translate them into practical recommendations for educational practice and policy.
- Supervise and mentor junior researchers and research assistants.
- Prepare and submit research proposals for funding to government agencies and foundations.
- Publish research findings in high-impact, peer-reviewed journals.
- Present research at national and international academic conferences.
- Collaborate with cross-functional teams to develop and evaluate educational interventions.
- Stay current with the latest theoretical and empirical advances in educational psychology and related fields.
Qualifications:
- Ph.D. in Educational Psychology, Developmental Psychology, or a related discipline with a strong research focus.
- Minimum of 8 years of post-doctoral research experience in an academic or research institution.
- Extensive experience in designing and conducting quantitative and qualitative educational research.
- Proficiency in statistical analysis software (e.g., SPSS, R, Stata) and data visualization tools.
- Demonstrated track record of securing research funding through grant applications.
- Strong publication record in reputable academic journals.
- Excellent written and verbal communication skills, with the ability to convey complex research ideas to diverse audiences.
- Experience in leading research teams and managing research projects.
- Familiarity with learning management systems and educational data analysis techniques.
This is a unique opportunity to make a significant contribution to the field of education research and drive meaningful change. Our client offers a competitive salary, excellent benefits, and the flexibility of a fully remote work environment.
This advertiser has chosen not to accept applicants from your region.
3
Senior Research Fellow - Educational Psychology
390001 Vadodara, Gujarat
₹60000 Annually
WhatJobs
Posted 23 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and insightful Senior Research Fellow specializing in Educational Psychology for a research initiative based in Vadodara, Gujarat, IN . This role involves designing and conducting research studies focused on learning processes, student engagement, and pedagogical effectiveness. The ideal candidate will have a strong academic background, excellent research methodology skills, and the ability to analyze complex educational data. You will contribute significantly to the understanding and improvement of educational practices through rigorous scientific inquiry.
Key responsibilities include:
A Ph.D. in Educational Psychology, Psychology, or a related field is required, with a minimum of 5 years of post-doctoral research experience. Proven experience in designing and conducting empirical research, strong statistical analysis skills, and a publication record in reputable academic journals are essential. Familiarity with learning management systems and educational technology is advantageous. Excellent written and verbal communication skills, as well as strong organizational and project management abilities, are critical.
Key responsibilities include:
- Designing and implementing research projects in educational psychology, focusing on areas such as cognitive development, learning theories, and student motivation.
- Developing research instruments, including surveys, questionnaires, and assessment tools.
- Collecting and analyzing quantitative and qualitative data using statistical software (e.g., SPSS, R).
- Interpreting research findings and drawing evidence-based conclusions.
- Writing comprehensive research reports, academic papers, and grant proposals.
- Disseminating research findings through presentations at conferences and publications in peer-reviewed journals.
- Collaborating with educators, students, and other researchers on research endeavors.
- Managing research timelines, budgets, and resources effectively.
- Ensuring ethical conduct of research, including obtaining necessary approvals and ensuring participant confidentiality.
- Staying abreast of the latest research and theories in educational psychology and related fields.
- Contributing to the development of innovative educational interventions and strategies based on research outcomes.
- Mentoring junior researchers or graduate students involved in the project.
- Assisting in the review of research proposals and manuscripts from other scholars.
- Contributing to the overall academic and research mission of the institution.
A Ph.D. in Educational Psychology, Psychology, or a related field is required, with a minimum of 5 years of post-doctoral research experience. Proven experience in designing and conducting empirical research, strong statistical analysis skills, and a publication record in reputable academic journals are essential. Familiarity with learning management systems and educational technology is advantageous. Excellent written and verbal communication skills, as well as strong organizational and project management abilities, are critical.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
Mumbai, Maharashtra
Bristol Myers Squibb
Posted today
Job Viewed
Job Description
**Working with Us**
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
**Job Title/Role : Clinical Research Associate**
Position Summary: The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements.
**Duties/Responsibilities:**
+ Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP
+ Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites
+ Monitor site adherence to ICH GCP and local regulations, including compliance with the principles of ALCOA to maintain data integrity and reliability. Where required, provide training and support to site staff to uphold these standards and ensure patient safety. Participate in sponsor and/or Health Authority audits and inspections as applicable.
+ Cultivate and sustain effective relationships with internal cross-functional teams and external partners, including vendors, clinical sites, and key stakeholders. Serve as the organization's representative for clinical trials at the site level.
+ Motivate and influence sites to meet study objectives, including enrollment and retention goals.
+ Communicate effectively, adapting to meet the needs of different stakeholders, utilizing the most appropriate communication style and method
+ Prepare and submit written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner
+ Assess potential Investigators and their sites to ensure sufficient resources and capabilities to conduct clinical trials. May identify new potential Investigators and/or sites through ongoing collaborations with internal and external stakeholders during the site feasibility and selection process.
+ Demonstrate understanding and proficiency working with targeted, centralized, remote and risk-based monitoring approaches
+ Identify, assess, and prioritize risks at the site and study level and support sites in mitigating issues, including implementing mitigation strategies based on risk indicators
+ Utilize strong analytical skills to evaluate site data and operational metrics, including ability to adjust monitoring strategies based on data trends and site performance
+ Where applicable, perform Unblinded Site Monitor activities to protect the blind of the study by acting as secondary monitoring source separate from the blinded monitor
+ Accountable for the review, reconciliation, and oversight of study drug/IMP. May support study drug/IMP label translation needs as applicable.
+ Involvement in Regulatory Compliance audit/inspection process, as needed. This includes the development and implementation of site corrective and preventive actions.
+ May support Ethics Committee submissions, ICF reviews, collection of documents to/from site
+ Support provision of access to relevant BMS and vendor systems is available for clinical trial site personnel and ensures internal BMS systems are kept up to date for site monitoring activities.
+ Support coordination of site activities related to database locks to ensure timelines are met as required locally.
+ Perform timely site closure activities when all required protocol visits and follow-up are completed.
**Qualifications:**
+ Bachelor's degree required, preferably within life sciences or equivalent
+ Valid driver's license (as locally required)
**Experience:**
+ Clinical Research Associate: 2-3 years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role.
+ Relevant prior Pharma/Biotech Sponsor employment or experience as a clinical study coordinator preferred
+ Experience in the drug discovery/development process.
**Competencies:**
+ Knowledge and understanding of clinical research processes, regulations and methodology
+ Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management
+ Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations (that govern clinical trials, with the ability to apply regulatory requirements to ensure compliance in clinical research activities ( Analytical thinking/critical thinking skills. Capable of using technology to analyze diverse and complex data sets, identify issues, trends, and outliers to develop effective solutions ( Demonstrate adaptability and a growth mindset by quickly learning and applying new technologies, embracing evolving methodologies, and remaining open to innovative ways of working in a dynamic environment
+ Organization and time management skills
+ Ability to build, maintain and strengthen relationships even under pressure and/ or in difficult situations with internal and external stakeholders
+ Good verbal and written communication skills (both in English and local language)
+ Have a foundational level of disease understanding and awareness (how the protocol fits in current landscape, standard of care, etc.)
+ Proven ability to work independently with a high degree of autonomy, proactively managing tasks and seeking opportunities for continuous learning
+ Ability to manage multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory
+ Proficient in navigating and utilizing multiple clinical systems (e.g., CTMS, eTMF, RBQM dashboards) to identify and resolve issues, support site performance, and ensure data integrity
**Software that must be used independently and without assistance:**
+ Microsoft Suite
+ Clinical Trial Management Systems (CTMS)
+ Electronic Data Capture Systems (eDC)
+ Electronic Trial Master File (eTMF)
+ RBM tools and platforms (e.g., Veeva, Medidata, CluePoints).
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
**Company:** Bristol-Myers Squibb
**Req Number:** R
**Updated:** :00:59.538 UTC
**Location:** Mumbai-IN
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
**Job Title/Role : Clinical Research Associate**
Position Summary: The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements.
**Duties/Responsibilities:**
+ Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP
+ Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites
+ Monitor site adherence to ICH GCP and local regulations, including compliance with the principles of ALCOA to maintain data integrity and reliability. Where required, provide training and support to site staff to uphold these standards and ensure patient safety. Participate in sponsor and/or Health Authority audits and inspections as applicable.
+ Cultivate and sustain effective relationships with internal cross-functional teams and external partners, including vendors, clinical sites, and key stakeholders. Serve as the organization's representative for clinical trials at the site level.
+ Motivate and influence sites to meet study objectives, including enrollment and retention goals.
+ Communicate effectively, adapting to meet the needs of different stakeholders, utilizing the most appropriate communication style and method
+ Prepare and submit written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner
+ Assess potential Investigators and their sites to ensure sufficient resources and capabilities to conduct clinical trials. May identify new potential Investigators and/or sites through ongoing collaborations with internal and external stakeholders during the site feasibility and selection process.
+ Demonstrate understanding and proficiency working with targeted, centralized, remote and risk-based monitoring approaches
+ Identify, assess, and prioritize risks at the site and study level and support sites in mitigating issues, including implementing mitigation strategies based on risk indicators
+ Utilize strong analytical skills to evaluate site data and operational metrics, including ability to adjust monitoring strategies based on data trends and site performance
+ Where applicable, perform Unblinded Site Monitor activities to protect the blind of the study by acting as secondary monitoring source separate from the blinded monitor
+ Accountable for the review, reconciliation, and oversight of study drug/IMP. May support study drug/IMP label translation needs as applicable.
+ Involvement in Regulatory Compliance audit/inspection process, as needed. This includes the development and implementation of site corrective and preventive actions.
+ May support Ethics Committee submissions, ICF reviews, collection of documents to/from site
+ Support provision of access to relevant BMS and vendor systems is available for clinical trial site personnel and ensures internal BMS systems are kept up to date for site monitoring activities.
+ Support coordination of site activities related to database locks to ensure timelines are met as required locally.
+ Perform timely site closure activities when all required protocol visits and follow-up are completed.
**Qualifications:**
+ Bachelor's degree required, preferably within life sciences or equivalent
+ Valid driver's license (as locally required)
**Experience:**
+ Clinical Research Associate: 2-3 years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role.
+ Relevant prior Pharma/Biotech Sponsor employment or experience as a clinical study coordinator preferred
+ Experience in the drug discovery/development process.
**Competencies:**
+ Knowledge and understanding of clinical research processes, regulations and methodology
+ Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management
+ Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations (that govern clinical trials, with the ability to apply regulatory requirements to ensure compliance in clinical research activities ( Analytical thinking/critical thinking skills. Capable of using technology to analyze diverse and complex data sets, identify issues, trends, and outliers to develop effective solutions ( Demonstrate adaptability and a growth mindset by quickly learning and applying new technologies, embracing evolving methodologies, and remaining open to innovative ways of working in a dynamic environment
+ Organization and time management skills
+ Ability to build, maintain and strengthen relationships even under pressure and/ or in difficult situations with internal and external stakeholders
+ Good verbal and written communication skills (both in English and local language)
+ Have a foundational level of disease understanding and awareness (how the protocol fits in current landscape, standard of care, etc.)
+ Proven ability to work independently with a high degree of autonomy, proactively managing tasks and seeking opportunities for continuous learning
+ Ability to manage multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory
+ Proficient in navigating and utilizing multiple clinical systems (e.g., CTMS, eTMF, RBQM dashboards) to identify and resolve issues, support site performance, and ensure data integrity
**Software that must be used independently and without assistance:**
+ Microsoft Suite
+ Clinical Trial Management Systems (CTMS)
+ Electronic Data Capture Systems (eDC)
+ Electronic Trial Master File (eTMF)
+ RBM tools and platforms (e.g., Veeva, Medidata, CluePoints).
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
**Company:** Bristol-Myers Squibb
**Req Number:** R
**Updated:** :00:59.538 UTC
**Location:** Mumbai-IN
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
Sun Pharmaceuticals, Inc
Posted 2 days ago
Job Viewed
Job Description
**Job location:** Chennai
**YOUR TASKS AND RESPONSIBILITIES:**
+ Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts
+ Preparation and submission of study documents for EC permission for respective study across centers
+ Oversee & document IP dispensing, inventory management & reconciliation
+ Ensure timely site initiation, site monitoring, and site close-out activities are performed and respective reports are generated
+ Investigator and site personnel training on the Study protocol, procedures, and GCP principles
+ Ensure timely recruitment of trial participants and subsequent efficient and effective data entry, source data verification and query resolution
+ Ensure timely reporting of SAEs, SUSARs, and reporting of SAEs to all sites and investigators in alignment with regulations and Suns PV policies
+ Risk identification, analysis, and CAPA for sites not meeting expectations as per the plan
+ Co-ordinate with in-house or CRO partners for data management, statistical analysis, statistical analysis report & DBL
**WHO YOU ARE:**
+ Minimum qualification requirement is to have a Bachelor's or Masters degree in a health(1)related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health and/or Post-graduate Diploma in Clinical Research
+ Relevant experience of 1-5 years minimum in the field of Clinical Research
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
**YOUR TASKS AND RESPONSIBILITIES:**
+ Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts
+ Preparation and submission of study documents for EC permission for respective study across centers
+ Oversee & document IP dispensing, inventory management & reconciliation
+ Ensure timely site initiation, site monitoring, and site close-out activities are performed and respective reports are generated
+ Investigator and site personnel training on the Study protocol, procedures, and GCP principles
+ Ensure timely recruitment of trial participants and subsequent efficient and effective data entry, source data verification and query resolution
+ Ensure timely reporting of SAEs, SUSARs, and reporting of SAEs to all sites and investigators in alignment with regulations and Suns PV policies
+ Risk identification, analysis, and CAPA for sites not meeting expectations as per the plan
+ Co-ordinate with in-house or CRO partners for data management, statistical analysis, statistical analysis report & DBL
**WHO YOU ARE:**
+ Minimum qualification requirement is to have a Bachelor's or Masters degree in a health(1)related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health and/or Post-graduate Diploma in Clinical Research
+ Relevant experience of 1-5 years minimum in the field of Clinical Research
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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6
Clinical Research Coordinator
Bengaluru, Karnataka
ClinoGenesis Research Institute
Posted today
Job Viewed
Job Description
Clinical Research Coordinator (Freshers Only)
Location: Hybrid/work from home
Organization: Clinogenesis Research Organization
Department: Clinical Operations
Employment Type: Full-Time
About US
Clinogenesis Research Organization is a leading contract research organization committed to advancing clinical excellence and innovation. We partner with global clients to deliver high-quality, compliant, and ethically sound clinical research solutions. At Clinogenesis, we believe in nurturing new talent and providing a structured pathway for growth in the clinical research industry.
Position Overview
We are seeking motivated and detail-oriented Clinical Research Coordinators to join our Clinical Operations team. This entry-level position is designed for fresh graduates who wish to build a professional career in clinical research. The selected candidates will gain hands-on exposure to the execution and coordination of clinical trials in compliance with regulatory and ethical standards.
Key Responsibilities
- Assist in the coordination and conduct of clinical trials under supervision.
- Support investigators and site teams in maintaining protocol compliance and accurate data capture.
- Maintain essential trial documentation, logs, and case report forms in accordance with GCP and SOP requirements.
- Ensure adherence to ICH-GCP guidelines, applicable regulations, and ethical standards.
- Participate in organizational training, meetings, and performance reviews to enhance professional competence.
Eligibility Criteria
- Education: B.Pharm, M.Pharm, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or related healthcare disciplines.
- Experience: Freshers only (candidates with prior industry experience will not be considered).
- Strong communication, documentation, and organizational skills.
- High level of integrity, attention to detail, and eagerness to learn.
What We Offer
- Structured onboarding and mentorship under industry experts.
- Exposure to global clinical operations and regulatory practices.
- Continuous professional training and growth opportunities.
Apply now or send your resume to
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7
Clinical Research Coordinator
Delhi, Delhi
MS CLINICAL RESEARCH
Posted 6 days ago
Job Viewed
Job Description
About the Job
We are looking for passionate Clinical Research Coordinators (CRC) to join our growing team. This is an exciting opportunity for fresh graduates with a clinical research course or background in life sciences/pharmacy who want to build a career in clinical trials and research.
Position Details
Role: Clinical Research Coordinator
Location: Delhi
Employment Type : Full-time
Experience: Freshers with clinical research training or related background encouraged to apply!
Key Responsibilities
- Conduct clinical trials in compliance with ICH GCP and protocol guidelines.
- Support study start-up activities and assist with site initiation.
- Participate in recruitment and retention of study subjects.
- Complete and maintain source documents, CRFs, and logs accurately.
- Compile and update the Site Master File.
- Manage Investigational Products (IP), including accountability and shipping.
- Coordinate submissions and communication with the Ethics Committee.
- Update sponsors on study progress and prepare for monitoring visits.
- Perform other responsibilities assigned by management.
Who Can Apply
- Freshers with a completed Clinical Research course.
- Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields.
- Strong interest in clinical trials and regulatory compliance.
- Excellent organisational, communication, and documentation skills.
Why Join Us?
Gain hands-on experience in clinical trials.
Learn directly from experienced professionals.
Be part of innovative projects that shape the future of healthcare.
A great opportunity to grow your career in clinical research.
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8
Clinical Research Associate
122001 Gurgaon, Haryana
₹650000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate to join their team in **Gurugram, Haryana, IN**. This critical role involves overseeing and managing clinical trials to ensure data accuracy, patient safety, and adherence to regulatory guidelines. You will be responsible for site selection and initiation, monitoring study progress, and ensuring compliance with protocols and Good Clinical Practice (GCP) standards. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory requirements, and medical terminology. Excellent organizational, communication, and interpersonal skills are essential for effective site management and data collection. Responsibilities include conducting routine site visits, resolving issues at study sites, verifying source documentation against case report forms, and ensuring timely data entry. You will also be responsible for managing study supplies and ensuring the ethical conduct of research. This is an on-site position requiring regular travel to clinical trial sites. We are looking for a proactive individual with a keen eye for detail and a commitment to scientific integrity. The ability to manage multiple studies simultaneously and maintain strong relationships with investigators and site staff is crucial. This is an exciting opportunity to contribute to the development of life-saving therapies and advance your career in pharmaceutical research within a reputable organization. You will play a vital role in bringing innovative treatments from development to market, ensuring the highest standards of safety and efficacy are met throughout the clinical trial process.
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