6,457 Clinical Trial Managers jobs in India

Greetings from HCL Technologies!

About the Company

HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver innovative solutions that drive business transformation and enhance customer experiences.

About the Role

We are looking for talented individuals to join our team and contribute to our mission of delivering exceptional technology solutions.

Responsibilities

• Bachelor’s degree in Life Sciences, Computer Science, or related field.
• 8+ years of experience in clinical data testing and validation.
• Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.
• Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
• Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
• Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
• Strong experience with clinical study setup and CDMS platforms and CTMS
• Review edit check specifications; write and execute UAT scripts.
• Conduct QC on metadata listings and peer review of programming checks.
• Support automation tool validation and standardization of test scripts.
• Ensure consistent use of clinical data standards across programs and repositories.
• Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
• Ensure compliance with GxP/GcP and internal SOPs.
• Document and share study-related testing deliverables and lessons learned
• Solid understanding of SDLC, validation methodology, and document management
• .

Pay range and compensation package

The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement

HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidates please drop mail to " "

``

Greetings from HCL Technologie!

About the Company

HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver technology solutions that drive business transformation and create value for our clients.

About the Role

We are looking for a talented individual to join our team and contribute to our mission of delivering innovative technology solutions.

Responsibilities

• Bachelor’s degree in Life Sciences, Computer Science, or related field.
• 6+ years of experience in clinical data testing and validation.
• Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.
• Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
• Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
• Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
• Strong experience with clinical study setup and CDMS platforms and CTMS
• Review edit check specifications; write and execute UAT scripts.
• Conduct QC on metadata listings and peer review of programming checks.
• Support automation tool validation and standardization of test scripts.
• Ensure consistent use of clinical data standards across programs and repositories.
• Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
• Ensure compliance with GxP/GcP and internal SOPs.
• Document and share study-related testing deliverables and lessons learned
• Solid understanding of SDLC, validation methodology, and document management

Qualifications

• Bachelor's degree in Computer Science or a related field.
• Relevant certifications are a plus.

Location - PAN INDIA

Pay range and compensation package

The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement

HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidate please drop mail to " "

Regards.

Suganya Periyasamy

``

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 Associate (Freshers Only)

Location: (Insert City or "Across India" if remote/hybrid)

Organization: Clinogenesis Research Organization

Department: Clinical operations

Type: Full-Time

About the Role:

Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research Associate.

Please note: This position is strictly for freshers. Candidates with prior experience are not eligible for this role.

If you’re passionate about clinical research and eager to grow in a structured, accredited environment, we invite you to apply.

Key Responsibilities:

• Assist with on-site coordination of clinical trial activities under supervision
• Maintain essential documents, site files, and case report forms
• Support the investigator in protocol compliance and patient coordination
• Ensure all trial activities adhere to ICH-GCP and ethical guidelines
• Participate in training sessions and team meetings as part of learning

Eligibility Criteria:

• Education: , B pharma , M pharma, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
• Experience: Freshers only
• Strong communication and organizational skills
• Eagerness to learn and grow in the clinical research domain

Why Start at Clinogenesis?

• Work alongside expert mentors and gain practical exposure
• Structured learning in a globally accredited research setup
• Continuous development and support for long-term career growth

Greetings from HCL Technologies!

About the Company

HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver innovative solutions that drive business transformation and enhance customer experiences.

About the Role

We are looking for talented individuals to join our team and contribute to our mission of delivering exceptional technology solutions.

Responsibilities

• Bachelor’s degree in Life Sciences, Computer Science, or related field.
• 8+ years of experience in clinical data testing and validation.
• Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.
• Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
• Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
• Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
• Strong experience with clinical study setup and CDMS platforms and CTMS
• Review edit check specifications; write and execute UAT scripts.
• Conduct QC on metadata listings and peer review of programming checks.
• Support automation tool validation and standardization of test scripts.
• Ensure consistent use of clinical data standards across programs and repositories.
• Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
• Ensure compliance with GxP/GcP and internal SOPs.
• Document and share study-related testing deliverables and lessons learned
• Solid understanding of SDLC, validation methodology, and document management
• .

Pay range and compensation package

The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement

HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidates please drop mail to " "

``

Greetings from HCL Technologie!

About the Company

HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver technology solutions that drive business transformation and create value for our clients.

About the Role

We are looking for a talented individual to join our team and contribute to our mission of delivering innovative technology solutions.

Responsibilities

• Bachelor’s degree in Life Sciences, Computer Science, or related field.
• 6+ years of experience in clinical data testing and validation.
• Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.
• Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
• Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
• Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
• Strong experience with clinical study setup and CDMS platforms and CTMS
• Review edit check specifications; write and execute UAT scripts.
• Conduct QC on metadata listings and peer review of programming checks.
• Support automation tool validation and standardization of test scripts.
• Ensure consistent use of clinical data standards across programs and repositories.
• Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
• Ensure compliance with GxP/GcP and internal SOPs.
• Document and share study-related testing deliverables and lessons learned
• Solid understanding of SDLC, validation methodology, and document management

Qualifications

• Bachelor's degree in Computer Science or a related field.
• Relevant certifications are a plus.

Location - PAN INDIA

Pay range and compensation package

The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement

HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidate please drop mail to " "

Regards.

Suganya Periyasamy

``

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

Job Role : Clinical Research Associate - Study Personnel (Toxicology & Efficacy)Location: Dholka, GujaratJob Responsibilities :1. Request for required no. of animals2. Observe the study animals for clinical signs, functional observation battery andmortality3. Receipt, storage and handling of chemicals, reagents and solutions4. Dose preparation and dosing of animals via different routs5. Weighing of animals, feed consumption, body temperature, dermal observations6. Randomization of study animals7. Perform pharma-efficacy studies like batch release test i.e., Pyrogen test, Abnormaltoxicity test, Potency assays, nodule test etc.8. Blood collection, separation and storage of samples9. Preparation of study reports10. 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 study14. Data entry from raw data to computer application and further analysis15. Co-operate during internal, RQA & sponsor audits of study plans, studies, data,reports etc.16. To participate in standardization of new toxicity study17. 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 ofGLP.3. Maintenance of internal records as per in-house SOPs and GLP4. Update and maintain training records5. 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 thedocumentation7. Prepare / revise the SOPs as and when required in accordance with in-house SOP8. Archive the documents as per in-house SOPs when applicable9. Document the deviation from study plan or SOP and report the incident to SD orHOS.10. Record the raw data as and when activities are performed, verify the data andcalculation.11. Results compilation and analysisInstrument handling and maintenance:1. Operate the instruments in accordance with respective instrument SOP, monitorcalibration & maintenance of instrumentation in lab2. Perform the calibration / maintenance of instruments as per in-house SOP