434 Psychology Research jobs in India
Psychology Research & Content Writing
Posted today
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Job Description
**Required Skills**:
- Ctc 10lacs - 13lacs
- 2years
- 5 years of experience (Not below 2 years)
- Any experience in creating assessment tool, analysing data, report writing, research etc.,
- Master’s in Psychology, Counselling or Social Work with a paper on Psychometrics and Statistics.
**Knowledge**
- Counselling Psychology, Psychology
- In depth understanding of psychometric concepts
- Familiarity with psychometric and analytic software/tools,
- Deploying assessments to large cohorts through the digital medium
**Professional**
- Ability to work on tight deadlines in a fast-paced environment
- Able to work independently, as well as in a team
- Constructing and designing assessment tools related to emotional wellbeing, mental health and illness, workplace wellbeing etc., for individuals, groups and at organizational level.
- Reviewing and updating the existing assessment tools
- Training counsellors on assessments
- Analysing data, Creating reports at individual, group and organizational level
- Connecting with sponsors/customers to understand the requirement
- Running essential pilot studies
- Administrative work related to the above tasks
- Run validity and reliability tests
**About Company**:
Founded in 2001, 1to1help.net is India's leading Employee Assistance Program (EAP) provider. We offer Psychological Counselling and comprehensive Wellness solutions that help employees deal with various work-life challenges like stress, anxiety, parenting, relationship issues both pre & post marital, work-life balance, etc. We currently support 800 clients and cover 1.5 million lives through our team of 250+ counsellors across 60+ locations in India.
**Salary**: ₹1,000,000.00 - ₹1,300,000.00 per year
Schedule:
- Day shift
**Experience**:
- any one in creating assessment tool, analysing data,: 2 years (required)
- Any one in report writing, research: 2 years (preferred)
License/Certification:
- Master’s in Psychology, Counselling or Social Work (required)
- Master with a paper on Psychometrics and Statistics. (required)
- experience in Assessment tools (required)
- Experience in Pyshcometric Concepts (required)
- Experience in Counselling (required)
- Comfortable with ctc 10lacs - 13lacs (required)
Academic Research Writer-psychology
Posted today
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Job Description
**Requirements**:
Ability to deliver plagiarism free assignments.
Good writing and analytical skills.
Efficiency with internet browsing and internet researching skills.
Submitting the solutions of the assignments within deadlines.
Reading the requirements very carefully before working on assignments.
**Eligibility**:
Msc/ MA in Psychology
**Relevant experience in the same industry preferred.**
Job type : Full-time & work from office.
Pay: ₹20,000.00 - ₹30,000.00 per month
**Benefits**:
- Flexible schedule
- Health insurance
- Leave encashment
- Paid sick time
- Paid time off
- Provident Fund
Schedule:
- Day shift
- Morning shift
- Night shift
Supplemental Pay:
- Overtime pay
- Performance bonus
- Quarterly bonus
- Shift allowance
- Yearly bonus
Senior Research Fellow - Educational Psychology
Posted today
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Job Description
As a Senior Research Fellow, you will lead and contribute to significant research projects focused on understanding and improving learning processes, student motivation, and pedagogical approaches. Your responsibilities will include designing research methodologies, collecting and analyzing data using statistical software, and disseminating findings through peer-reviewed publications and conference presentations. You will mentor junior researchers and PhD students, guiding them through their research endeavors. A critical aspect of this role involves securing research grants and managing project budgets effectively. You will also play a key role in developing new research proposals and fostering collaborations with academic institutions and educational stakeholders both domestically and internationally. The ideal candidate will possess a deep understanding of educational psychology theories, advanced quantitative and qualitative research skills, and a strong publication record. Excellent analytical, problem-solving, and written communication skills are essential. This position requires a proactive, independent researcher with the ability to work effectively within a collaborative academic environment.
Key Responsibilities:
- Design and conduct rigorous research studies in educational psychology.
- Collect, analyze, and interpret complex educational data using statistical software (e.g., SPSS, R).
- Author high-quality research papers for publication in leading academic journals.
- Present research findings at national and international conferences.
- Mentor and supervise junior researchers and graduate students.
- Write grant proposals to secure funding for new research projects.
- Collaborate with educators and policymakers to translate research into practice.
- Stay abreast of current trends and advancements in educational psychology and research methodologies.
- Ph.D. in Educational Psychology, Psychology, or a closely related field.
- Minimum of 6 years of post-doctoral research experience.
- Demonstrated success in securing research grants and managing research projects.
- A strong portfolio of publications in reputable peer-reviewed journals.
- Expertise in advanced statistical analysis and research design.
- Excellent written and verbal communication skills.
- Experience in mentoring junior researchers is highly desirable.
- Ability to work independently and collaboratively in an academic setting.
Clinical Research Physician
Posted 3 days ago
Job Viewed
Job Description
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
Clinical Research Associate
Posted today
Job Viewed
Job Description
Job Role : Clinical Research Associate - Study Personnel (Toxicology & Efficacy)
Location: Dholka, Gujarat
Job Responsibilities :
1. Request for required no. of animals
2. Observe the study animals for clinical signs, functional observation battery and
mortality
3. Receipt, storage and handling of chemicals, reagents and solutions
4. Dose preparation and dosing of animals via different routs
5. Weighing of animals, feed consumption, body temperature, dermal observations
6. Randomization of study animals
7. Perform pharma-efficacy studies like batch release test i.e., Pyrogen test, Abnormal
toxicity test, Potency assays, nodule test etc.
8. Blood collection, separation and storage of samples
9. Preparation of study reports
10. Conduct of study, data collection, compilation and verification.
11. Collection of sample(s) / Specimen(s).
12. Preparation and verification of report.
13. To participate in Genotoxicity study
14. Data entry from raw data to computer application and further analysis
15. Co-operate during internal, RQA & sponsor audits of study plans, studies, data,
reports etc.
16. To participate in standardization of new toxicity study
17. Ensure proper labeling of containers (test item, samples etc.)
Documentation:
1. To document deviation from SOP or study plan and communicate directly with SD.
2. Recording raw data promptly and accurately and in compliance with Principles of
GLP.
3. Maintenance of internal records as per in-house SOPs and GLP
4. Update and maintain training records
5. Ensuring the availability of various monitoring certificates such as feed, water,
bedding material, health etc.
6. Request for the issuance of controlled / uncontrolled document and maintain the
documentation
7. Prepare / revise the SOPs as and when required in accordance with in-house SOP
8. Archive the documents as per in-house SOPs when applicable
9. Document the deviation from study plan or SOP and report the incident to SD or
HOS.
10. Record the raw data as and when activities are performed, verify the data and
calculation.
11. Results compilation and analysis
Instrument handling and maintenance:
1. Operate the instruments in accordance with respective instrument SOP, monitor
calibration & maintenance of instrumentation in lab
2. Perform the calibration / maintenance of instruments as per in-house SOP
Clinical Research Executive
Posted 3 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.
Clinical Research Associate
Posted today
Job Viewed
Job Description
Job Role : Clinical Research Associate - Study Personnel (Toxicology & Efficacy)
Location: Dholka, Gujarat
Job Responsibilities :
1. Request for required no. of animals
2. Observe the study animals for clinical signs, functional observation battery and
mortality
3. Receipt, storage and handling of chemicals, reagents and solutions
4. Dose preparation and dosing of animals via different routs
5. Weighing of animals, feed consumption, body temperature, dermal observations
6. Randomization of study animals
7. Perform pharma-efficacy studies like batch release test i.e., Pyrogen test, Abnormal
toxicity test, Potency assays, nodule test etc.
8. Blood collection, separation and storage of samples
9. Preparation of study reports
10. Conduct of study, data collection, compilation and verification.
11. Collection of sample(s) / Specimen(s).
12. Preparation and verification of report.
13. To participate in Genotoxicity study
14. Data entry from raw data to computer application and further analysis
15. Co-operate during internal, RQA & sponsor audits of study plans, studies, data,
reports etc.
16. To participate in standardization of new toxicity study
17. Ensure proper labeling of containers (test item, samples etc.)
Documentation:
1. To document deviation from SOP or study plan and communicate directly with SD.
2. Recording raw data promptly and accurately and in compliance with Principles of
GLP.
3. Maintenance of internal records as per in-house SOPs and GLP
4. Update and maintain training records
5. Ensuring the availability of various monitoring certificates such as feed, water,
bedding material, health etc.
6. Request for the issuance of controlled / uncontrolled document and maintain the
documentation
7. Prepare / revise the SOPs as and when required in accordance with in-house SOP
8. Archive the documents as per in-house SOPs when applicable
9. Document the deviation from study plan or SOP and report the incident to SD or
HOS.
10. Record the raw data as and when activities are performed, verify the data and
calculation.
11. Results compilation and analysis
Instrument handling and maintenance:
1. Operate the instruments in accordance with respective instrument SOP, monitor
calibration & maintenance of instrumentation in lab
2. Perform the calibration / maintenance of instruments as per in-house SOP
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Clinical Research Executive
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.
Clinical Research Associate
Posted today
Job Viewed
Job Description
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.
Clinical Research Associate
Posted today
Job Viewed
Job Description
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.