452 Clinical Trial Processes jobs in India
Clinical Research Physician
Chennai, Tamil Nadu
ICON Clinical Research
Posted 3 days ago
Job Viewed
Job Description
Clinical Research Physician
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Job Advert Posting
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
**JOB FUNCTIONS/RESPONSIBILITIES:**
+ Serve as medical team leader on assigned projects,
+ Ensure provision of all contracted activities and identification of out of scope activities on projects assigned
+ Medical review of clinical trial data, including review of Laboratory alerts, Electrocardiogram (ECG) alerts, data from eCRF/ EDC (listing review/ Patient profile review), Eligibility review, Identify protocol deviations, coding review and preparation of Medical Monitoring Reports as per requirement
+ Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following:
+ Medical information source
+ Ongoing training for project teams in therapeutic areas as requested
+ Review of study documentation (protocol, CRF. etc.)
+ Contribute to investigator meeting presentations
+ Ongoing safety review of individual patient laboratory reports generated by central laboratories
+ CRF safety review
+ Contribute any necessary medical input into integrated clinical and statistical reports
+ Assist in making presentations to potential clients when appropriate
+ Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs
+ Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations
+ Represent ICON Medical Affairs at teleconferences and meetings
+ Liaise with Sponsors regarding medical issues and medical consultation
+ Ensure quality of medical deliverables in accordance with project plans and ICON Standards
+ Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention
**QUALIFICATIONS/EXPERIENCE REQUIRED:**
+ To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
+ Medical degree and broad based post graduate clinical experience
+ Solid work experience in a relevant role, ability to medically evaluate clinical data, and good analytical skills
+ Proficiency in English, Good oral and written communication skills
+ Ability and willingness to travel on an as-need basis
+ Excellent presentation skills
+ Good computer skills (MS: Outlook, Word, Excel)
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Job Advert Posting
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
**JOB FUNCTIONS/RESPONSIBILITIES:**
+ Serve as medical team leader on assigned projects,
+ Ensure provision of all contracted activities and identification of out of scope activities on projects assigned
+ Medical review of clinical trial data, including review of Laboratory alerts, Electrocardiogram (ECG) alerts, data from eCRF/ EDC (listing review/ Patient profile review), Eligibility review, Identify protocol deviations, coding review and preparation of Medical Monitoring Reports as per requirement
+ Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following:
+ Medical information source
+ Ongoing training for project teams in therapeutic areas as requested
+ Review of study documentation (protocol, CRF. etc.)
+ Contribute to investigator meeting presentations
+ Ongoing safety review of individual patient laboratory reports generated by central laboratories
+ CRF safety review
+ Contribute any necessary medical input into integrated clinical and statistical reports
+ Assist in making presentations to potential clients when appropriate
+ Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs
+ Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations
+ Represent ICON Medical Affairs at teleconferences and meetings
+ Liaise with Sponsors regarding medical issues and medical consultation
+ Ensure quality of medical deliverables in accordance with project plans and ICON Standards
+ Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention
**QUALIFICATIONS/EXPERIENCE REQUIRED:**
+ To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
+ Medical degree and broad based post graduate clinical experience
+ Solid work experience in a relevant role, ability to medically evaluate clinical data, and good analytical skills
+ Proficiency in English, Good oral and written communication skills
+ Ability and willingness to travel on an as-need basis
+ Excellent presentation skills
+ Good computer skills (MS: Outlook, Word, Excel)
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Executive
Hyderabad, Andhra Pradesh
Apex CoVantage
Posted 2 days ago
Job Viewed
Job Description
Designation: Clinical Research Executive
Department: Clinical Research
Role Overview:
Specialized in pharmaceutical research and competitive intelligence, with expertise in drug development, clinical trial analytics, and regulatory insights — delivering accurate data.
Key Responsibilities:
Conduct secondary research on drugs, mechanisms, targets, and indications; track innovative drug pipelines, regulatory updates, and clinical trials.
Analyze, maintain, and validate pharmaceutical databases with accuracy on key fields such as drug names, MOA, sponsors, molecule types, and trial data.
Monitor developments from regulatory bodies (US FDA, EMA, CDE, etc.), industry reports, patents, and company filings to provide usable and intellectual data.
Prepare weekly/monthly reports, databooks, and dashboards; deliver strategic recommendations on training the team on accurate data capture and address client queries.
Collect and analyze information from trial registries, filtering by condition, intervention, phase, and recruitment status; capture critical study details such as endpoints, design, inclusion/exclusion criteria, and sponsor information.
Identify tool/process gaps, ensure compliance with company guidelines, and support capability building through training and knowledge sharing to enhance team performance.
Key Skills & Competencies
- Strong knowledge of clinical research methodologies, GCP, and regulatory requirements.
- Experience in drug safety and pharmacovigilance reporting.
- Excellent organizational, documentation, and project management skills.
- Strong interpersonal and communication skills to work effectively with internal teams and external stakeholders.
Qualifications & Experience
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
- 5–8 years of experience in clinical research and clinical trial management.
- Hands-on experience in managing clinical trial operations and regulatory submissions.
- Prior experience working in CROs, pharmaceutical, or biotechnology companies preferred.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Executive
Hyderabad, Andhra Pradesh
Apex CoVantage
Posted today
Job Viewed
Job Description
Designation: Clinical Research Executive
Department: Clinical Research
Role Overview:
Specialized in pharmaceutical research and competitive intelligence, with expertise in drug development, clinical trial analytics, and regulatory insights — delivering accurate data.
Key Responsibilities:
Conduct secondary research on drugs, mechanisms, targets, and indications; track innovative drug pipelines, regulatory updates, and clinical trials.
Analyze, maintain, and validate pharmaceutical databases with accuracy on key fields such as drug names, MOA, sponsors, molecule types, and trial data.
Monitor developments from regulatory bodies (US FDA, EMA, CDE, etc.), industry reports, patents, and company filings to provide usable and intellectual data.
Prepare weekly/monthly reports, databooks, and dashboards; deliver strategic recommendations on training the team on accurate data capture and address client queries.
Collect and analyze information from trial registries, filtering by condition, intervention, phase, and recruitment status; capture critical study details such as endpoints, design, inclusion/exclusion criteria, and sponsor information.
Identify tool/process gaps, ensure compliance with company guidelines, and support capability building through training and knowledge sharing to enhance team performance.
Key Skills & Competencies
- Strong knowledge of clinical research methodologies, GCP, and regulatory requirements.
- Experience in drug safety and pharmacovigilance reporting.
- Excellent organizational, documentation, and project management skills.
- Strong interpersonal and communication skills to work effectively with internal teams and external stakeholders.
Qualifications & Experience
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
- 5–8 years of experience in clinical research and clinical trial management.
- Hands-on experience in managing clinical trial operations and regulatory submissions.
- Prior experience working in CROs, pharmaceutical, or biotechnology companies preferred.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate
400601 Thane, Maharashtra
₹60000 month
WhatJobs
Posted today
Job Viewed
Job Description
Are you a detail-oriented and experienced professional in the pharmaceutical or clinical research field? Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a motivated Clinical Research Associate (CRA) to join their team in Thane, Maharashtra, IN . This role offers a hybrid working model, combining the benefits of remote flexibility with essential on-site collaboration. As a CRA, you will play a crucial role in ensuring the quality and integrity of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out activities, building strong relationships with investigators and site staff. Your key duties will include reviewing patient records, ensuring proper documentation, and reporting trial progress. The ideal candidate will possess a strong understanding of clinical trial processes, excellent organizational and communication skills, and the ability to travel to study sites as needed. A background in life sciences, nursing, or a related field, coupled with prior experience as a CRA or in a clinical research support role, is essential. We are looking for individuals who are proactive, analytical, and committed to upholding the highest ethical and scientific standards. This is an excellent opportunity to contribute to the development of life-saving therapies and grow your career within a reputable organization. If you are driven by a passion for medical advancement and possess the required skills and experience, we encourage you to apply.
Key Responsibilities:
Key Responsibilities:
- Conduct site selection, initiation, interim monitoring, and close-out visits.
- Ensure adherence to protocols, SOPs, GCP, and regulatory requirements at study sites.
- Verify the accuracy, completeness, and integrity of clinical data.
- Manage communication and relationships with investigators and site staff.
- Train site personnel on study procedures and protocols.
- Review essential documents and regulatory binders.
- Prepare monitoring reports and track action items.
- Identify and escalate site-level issues and risks.
- Participate in investigator meetings and provide feedback.
- Ensure timely submission of study-related documentation.
- Proven experience as a Clinical Research Associate (CRA) or similar role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with clinical trial monitoring and site management.
- Strong understanding of medical terminology and clinical research processes.
- Excellent attention to detail and organizational skills.
- Proficiency in data management and electronic data capture (EDC) systems.
- Strong written and verbal communication skills.
- Ability to travel to sites as required.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Working knowledge of study documentation and regulatory submissions.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate
500001 Shaikpet, Andhra Pradesh
₹70000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is looking for a meticulous and experienced Clinical Research Associate (CRA) to join their team. This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will be responsible for monitoring trial sites, collecting data, and ensuring the safety and well-being of trial participants. This is a hybrid position, offering a balance of remote work and essential on-site monitoring activities at clinical trial locations in and around **Hyderabad, Telangana, IN**.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, SOPs, and regulatory guidelines (e.g., GCP, ICH).
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Perform source data verification (SDV) and review source documents.
- Manage communication between investigators, site staff, and the sponsor.
- Ensure timely submission of required study documents and reports.
- Oversee the recruitment and enrollment of study participants.
- Train site staff on study protocols and procedures.
- Identify and report adverse events and deviations from protocol.
- Conduct site initiation, monitoring, and close-out visits.
- Maintain organized and up-to-date trial documentation and site files.
- Collaborate with clinical operations teams and data management.
- Ensure the safety and rights of study participants are protected.
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field. Advanced degree is a plus.
- Minimum of 3-5 years of experience as a Clinical Research Associate or in a similar role.
- In-depth knowledge of clinical trial processes, GCP, and regulatory requirements.
- Excellent monitoring, data collection, and documentation skills.
- Strong understanding of medical terminology and disease states.
- Effective communication, interpersonal, and organizational abilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required for monitoring.
- Strong analytical and problem-solving skills.
- Commitment to ethical research practices.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
208001 Kanpur, Uttar Pradesh
₹800000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a global pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to support their ongoing clinical trials. This hybrid role involves regular site visits to hospitals and research centers in and around Kanpur, Uttar Pradesh , balanced with remote work for data management, reporting, and coordination. You will play a vital role in ensuring the quality and integrity of clinical trial data.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites to ensure adherence to Good Clinical Practice (GCP), protocols, and regulatory requirements.
- Verify the accuracy, completeness, and validity of clinical data collected at study sites.
- Conduct site initiation visits, routine monitoring visits, and close-out visits.
- Manage communication between investigative sites and the study team.
- Train site staff on study protocols, procedures, and data collection requirements.
- Ensure the proper handling and storage of investigational products and study-related materials.
- Identify, document, and resolve site-specific issues and deviations.
- Prepare monitoring reports and follow up on action items with site personnel.
- Facilitate drug accountability and maintain study documentation at investigator sites.
- Collaborate with study statisticians, data managers, and medical monitors.
- Ensure timely submission of all required study documents to regulatory authorities and ethics committees.
- Contribute to the development and review of study protocols and case report forms (CRFs).
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field. A Master's degree is preferred.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical or biotech industry.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong understanding of medical terminology and clinical trial processes.
- Excellent organizational skills, attention to detail, and ability to manage multiple priorities.
- Proficient in Microsoft Office Suite, particularly Word, Excel, and PowerPoint.
- Effective communication and interpersonal skills, with the ability to build strong relationships with site staff.
- Ability to travel frequently to clinical sites and work effectively in a hybrid environment.
- Problem-solving skills and the ability to work independently with minimal supervision.
- Experience in oncology or cardiovascular clinical trials is a significant advantage.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
226001 Lucknow, Uttar Pradesh
₹75000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in Lucknow, Uttar Pradesh . This role plays a vital part in ensuring the successful execution of clinical trials, adhering strictly to regulatory guidelines and protocols. The ideal candidate will be responsible for monitoring clinical trial sites, ensuring data accuracy, patient safety, and overall compliance with Good Clinical Practice (GCP) standards. Key responsibilities include site initiation visits, routine monitoring visits, and site closure visits. You will review patient records, source documents, and case report forms (CRFs) to verify data integrity. The CRA will also liaise with investigators and site staff, providing training and support as needed, and resolving any discrepancies or issues that arise. Effective communication and problem-solving skills are essential for managing relationships with multiple stakeholders. Travel to clinical trial sites will be a necessary component of this role, balanced with remote administrative tasks. Staying updated on evolving regulatory requirements and industry best practices is crucial. This position offers a compelling opportunity to contribute to the advancement of medical research and the development of life-saving therapies within a dynamic and professional setting. The successful applicant will demonstrate a strong commitment to ethical research conduct and patient well-being.
Key Qualifications:
If you are passionate about clinical research and possess the required expertise, we encourage you to apply.
Key Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Experience with clinical trial monitoring, site management, and data verification.
- Strong understanding of medical terminology and clinical research processes.
- Excellent communication, organizational, and time management skills.
- Ability to travel to sites as required.
- Proficiency in clinical trial management software and EDC systems is a plus.
If you are passionate about clinical research and possess the required expertise, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Research Scientist
700016 Kolkata, West Bengal
₹95000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
We are looking for a dedicated and meticulous Clinical Research Scientist to join our pharmaceutical team, operating on a fully remote basis. This pivotal role will involve designing, implementing, and managing clinical trials in accordance with regulatory guidelines and company objectives. You will be responsible for developing study protocols, ensuring the accurate collection and analysis of trial data, and preparing comprehensive study reports. Key responsibilities include collaborating with investigators and study coordinators to maintain data integrity, monitoring patient safety and adherence to study procedures, and managing the overall lifecycle of clinical research projects. The ideal candidate will have a strong scientific background, with a Master's or Ph.D. in a relevant life science discipline such as Pharmacology, Biology, or Biochemistry. Extensive experience in clinical trial management, a deep understanding of Good Clinical Practice (GCP) and regulatory requirements (e.g., FDA, EMA), and proven expertise in statistical analysis and data interpretation are essential. You will be expected to contribute to the scientific strategy of the company, identifying new research opportunities and contributing to the development of innovative therapies. Excellent written and verbal communication skills are necessary for preparing regulatory submissions, scientific publications, and presenting findings to diverse audiences. This remote position requires exceptional organizational skills, the ability to work autonomously, and a proactive approach to problem-solving. Join our innovative team and contribute to advancing healthcare through cutting-edge pharmaceutical research from the comfort of your home.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate
160001 Chandigarh, Chandigarh
₹75000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their growing research team. This is a fully remote position, offering the flexibility to conduct essential research activities from anywhere in India. As a CRA, you will play a critical role in overseeing and managing clinical trials, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as data collection and management. Your primary focus will be to ensure the safety and integrity of study participants and the accuracy of the data collected.
Key responsibilities include developing and finalizing clinical trial protocols, managing study documentation, and providing training to study site staff. You will serve as the main point of contact for investigators and study sites, addressing any queries or issues that arise during the trial. The role involves extensive travel to clinical sites across various regions, although the core responsibilities and management are conducted remotely. You will review source documents, electronic data capture (EDC) systems, and investigational product accountability to ensure data quality and compliance. This position requires strong organizational skills, meticulous attention to detail, and the ability to work independently while collaborating effectively with cross-functional teams. We are looking for an individual passionate about advancing medical research and committed to upholding the highest standards of ethical conduct and scientific rigor. Join our client and contribute to bringing life-changing therapies to patients.
Qualifications:
Key responsibilities include developing and finalizing clinical trial protocols, managing study documentation, and providing training to study site staff. You will serve as the main point of contact for investigators and study sites, addressing any queries or issues that arise during the trial. The role involves extensive travel to clinical sites across various regions, although the core responsibilities and management are conducted remotely. You will review source documents, electronic data capture (EDC) systems, and investigational product accountability to ensure data quality and compliance. This position requires strong organizational skills, meticulous attention to detail, and the ability to work independently while collaborating effectively with cross-functional teams. We are looking for an individual passionate about advancing medical research and committed to upholding the highest standards of ethical conduct and scientific rigor. Join our client and contribute to bringing life-changing therapies to patients.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical industry.
- In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulatory requirements.
- Experience with EDC systems and clinical trial management software.
- Excellent communication, interpersonal, and problem-solving skills.
- Ability to manage multiple priorities and meet strict deadlines in a remote work environment.
- Willingness to travel as required for site visits.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate
682001 Kochi, Kerala
₹850000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is actively recruiting a skilled Clinical Research Associate (CRA) to join their esteemed team in Kochi, Kerala . This role is integral to the successful execution of clinical trials, ensuring that they are conducted, recorded, and reported in accordance with protocol, standard operating procedures, and applicable regulatory requirements. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits. You will ensure that study protocols are adhered to, patient safety is maintained, and data integrity is upheld throughout the trial.
Key responsibilities include verifying data accuracy, managing investigational product, and ensuring compliance with Good Clinical Practice (GCP) guidelines. The CRA will build and maintain strong working relationships with clinical investigators and site staff, providing training and support as needed. Excellent written and verbal communication skills are essential for preparing monitoring reports, communicating with regulatory authorities, and collaborating with internal teams. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. A meticulous approach to documentation and a commitment to quality are paramount. This is an excellent opportunity for a dedicated professional to contribute to the development of life-saving medicines and advance their career in the dynamic pharmaceutical industry. We are looking for an individual who is proactive, detail-oriented, and capable of managing multiple priorities in a challenging yet rewarding environment.
Key responsibilities include verifying data accuracy, managing investigational product, and ensuring compliance with Good Clinical Practice (GCP) guidelines. The CRA will build and maintain strong working relationships with clinical investigators and site staff, providing training and support as needed. Excellent written and verbal communication skills are essential for preparing monitoring reports, communicating with regulatory authorities, and collaborating with internal teams. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. A meticulous approach to documentation and a commitment to quality are paramount. This is an excellent opportunity for a dedicated professional to contribute to the development of life-saving medicines and advance their career in the dynamic pharmaceutical industry. We are looking for an individual who is proactive, detail-oriented, and capable of managing multiple priorities in a challenging yet rewarding environment.
This advertiser has chosen not to accept applicants from your region.
9