8,521 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 " "

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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.

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

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.

Job Title : Clinical Research Associate (CRA)

Company : MS Clinical Research Pvt Ltd

Experience : Minimum 3 years

About Us :

MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical solutions.

Job Summary :

We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 3-5 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory requirements, and excellent communication and organizational skills.

Key Responsibilities :

Site Management :

Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory requirements. Build and maintain strong relationships with investigative sites, investigators, and study coordinators.

Clinical Trial Monitoring :

Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance. Ensure timely resolution of data queries and issues identified during monitoring visits.

Protocol Compliance :

Ensure that all study activities are conducted in accordance with the approved protocol, SOPs, and applicable regulatory guidelines. Collaborate with investigators to address and resolve protocol-related queries.

Regulatory Compliance :

Assist in the preparation and submission of regulatory documents to ethics committees and regulatory authorities. Stay informed about changes in regulatory requirements and update study teams accordingly.

Data Management :

Collaborate with data management teams to ensure accurate and timely data collection and entry.

Perform source data verification and data validation activities.

Safety Reporting :

Monitor and report adverse events in compliance with regulatory requirements and safety reporting procedures. Ensure that safety reports are submitted to relevant authorities and stakeholders.

Training and Support :

Provide training and support to site staff on study protocols, data collection, and regulatory compliance. Act as a resource for investigators and site staff throughout the duration of the study.

Requirements :

Education: Bachelor's degree in a relevant life sciences field.

Experience :

Minimum of 3 years of experience as a Clinical Research Associate.

Proven track record of successful site management and monitoring in clinical trials.

Regulatory Knowledge: Familiarity with regulatory requirements and guidelines governing clinical trials.

Communication Skills : Excellent verbal and written communication skills.

Organizational Skills : Strong organizational and time management skills with attention to detail.

Team Collaboration : Ability to work effectively in cross-functional teams and independently.

Travel : Willingness to travel to investigative sites as needed.

Benefits :

Competitive salary and benefits package.

Opportunities for professional development and advancement.

Collaborative and dynamic work environment.

Join our team at MS Clinical Research and contribute to the advancement of clinical research and the development of innovative healthcare solutions.

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 Title: Clinical Research Associate (Remote – MBBS/PhD Students)

Company: Synergy Health 360 – Research Department

Location: Remote (India-based applicants, U.S. time zone / India night shift)

About Us:

Synergy Health 360 is an innovative and expanding healthcare organization based in Arizona, USA. Our mission is to enhance patient outcomes while creating opportunities for medical professionals to grow academically and professionally. As part of our research initiatives, we are offering MBBS/PhD students the chance to contribute remotely to our U.S.-based research projects.

Why This Is a Win-Win Opportunity:

This role is structured like a clinical research rotation. Medical students and young researchers gain:

• Academic enhancement through hands-on research experience.
• International exposure to U.S. healthcare systems and practices.
• Strong credentials for career development, residency, or academic pursuits.

At the same time, Synergy Health 360 benefits from your expertise in Wound Care, Diabetes, and Cardiology research, creating a true partnership.

Position Overview:

We are seeking MBBS/PhD students with 2–3 years of prior research associate experience and specialization in Wound Care, Diabetes, or Cardiology. You will be working with our research department to support studies, data analysis, and publications aligned with U.S. healthcare objectives.

Key Responsibilities:

• Conduct research and literature reviews in wound care, diabetes, and cardiology.
• Analyze patient data and summarize findings for ongoing research studies.
• Collaborate with U.S.-based clinicians and researchers in real time.
• Prepare reports, presentations, and documentation to support academic publishing.

Mandatory Requirements:

• MBBS degree or PhD in medical/life sciences.
• 2–3 years of prior research associate experience.
• Demonstrated work in Wound Care, Diabetes, or Cardiology.
• Strong research, analytical, and documentation skills.
• Proficiency in English communication (written & verbal).
• Ability to work during U.S. hours (India night shift).

Probation Period:

• Initial 1-month trial/rotation period.
• Continued engagement based on performance review.

Compensation & Benefits:

• Depending on qualifications & experience
• Academic exposure through international research projects.
• Letters of recommendation and academic references available upon successful completion.
• Opportunity to enhance CV/residency applications with international research experience.

Job Type: Contractual / Temporary

Contract length: 12 months

Pay: Up to ₹1.00 per hour

Expected hours: 40 per week

Benefits:

• Flexible schedule
• Work from home

Expected Start Date: 06/10/2025

CRA Job Opening @ ICON – Bangalore.

ICON plc is hiring Clinical Research Associates (CRA) in Bangalore Be part of a global leader in healthcare intelligence & clinical research.

Know someone perfect for this?

Choudhary Waseem Jamil

Job Types: Full-time, Fresher

Pay: ₹100, ₹500,000.00 per year

Benefits:

• Internet reimbursement

Work Location: In person

About the Role

We are looking for a meticulous and motivated Clinical Research Associate (Trainee) to join our clinical research team. This entry-level role offers hands-on experience in monitoring and coordinating clinical trials, ensuring they comply with regulatory standards and protocol guidelines. The trainee will work closely with senior CRAs and clinical site staff to support the successful execution of clinical studies.

Key Responsibilities

• Assist in conducting site visits to monitor clinical trial progress, compliance, and data accuracy.
• Support documentation and management of clinical trial materials and regulatory submissions.
• Help ensure the protection and well-being of trial participants by adhering to Good Clinical Practice (GCP) guidelines.
• Collect, verify, and review case report forms (CRFs) and source data for completeness and accuracy.
• Coordinate with investigators, site staff, and sponsors to facilitate smooth trial operations.
• Participate in training and development sessions to build clinical trial management skills.
• Assist in preparing monitoring reports and trial documentation.
• Support the tracking of patient enrollment and follow-up activities.
• Maintain confidentiality and comply with ethical and regulatory requirements.

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, or related field.
• Interest in clinical research and healthcare.
• Strong attention to detail and organizational skills.
• Basic understanding of clinical trial processes and regulations is a plus.
• Good communication and interpersonal skills.
• Proficient in Microsoft Office applications.
• Ability to work independently and as part of a team.
• Willingness to travel as required for site visits.

Job Types: Full-time, Permanent, Fresher

Pay: ₹9, ₹20,407.06 per month

Work Location: In person

Role & responsibilities

To overall coordinate the activities of CPU at ARL.

To inform to the volunteer coordinator (from outside source) about the details of the study and confirm the participation of the required number of volunteers as per the study protocol. Preparation of trial master file, source documents, labels of the study.

To monitor the activities like dosing, sample collection and sample processing, during study activities.

To review synchronization of clock.

To co-ordinate outside laboratory.

To co-ordinate with canteen department related to study activities and its menu.

To review temperature and humidity records of sample collection area, sample processing area, housing area before initiation of the relevant activities. To maintain volunteer databank, age proof records.

To do all IP related activities like IMP Receipt, IMP acceptance, IMP dispensing and reconciliation etc.

To record and review the study documents.

To dose the subjects and monitor the posture restriction.

To report all study related deviations to the Principal Investigator.

To work as a authorized trained person in pharmacy activities.

Any other responsibilities assigned by the Principal Investigator.

Company Description

Novaspire Biosciences Private Limited is a healthcare company specializing in Pharmacovigilance, Clinical Research, and Bioavailability/Bioequivalence studies Project Management support. Novaspire is dedicated to enhancing patient safety and promoting public health through innovative solutions for the pharmaceutical and biotechnology industries. Our team of experienced professionals provides a wide range of services, including Pharmacovigilance, Clinical Research Consulting, and Regulatory Affairs Solutions.

Objectives of this role

• Ensuring compliance with protocols, standard operating procedures, and Good Clinical Practice (GCP) guidelines.
• Conducting regular site visits to monitor trial activities and data collection.
• Reviewing and analysing clinical trial data for accuracy and completeness.
• Developing and maintaining study timelines and budgets.
• Providing training to study staff on study protocols and GCP guidelines.

Your tasks

• Reviewing and approving study-related documents, such as informed consent forms.
• Conducting source data verification and ensuring data quality.
• Managing trial supplies and drug accountability.
• Serving as a liaison between study sites, sponsors and regulatory agencies.

Required skills and qualifications

• bachelor's/Master's degree in pharmacy.
• At least 1 year of experience in a similar role.
• Knowledge of regulatory requirements and guidelines, such as Good Clinical Practice (GCP) and International Council for Harmonization (ICH).
• Certification in clinical research, such as the Association of Clinical Research Professionals (ACRP) certification.
• Knowledge of clinical trial data management systems and electronic data capture.
• Experience with site selection, initiation, management, and monitoring activities.
• Strong attention to detail and accuracy in data management.

Preferred skills and qualifications

• Understanding of pharmacology and drug development processes.
• Working knowledge of medical terminology and anatomy.
• Excellent project management and leadership skills with attention to detail.
• Ability to work collaboratively with study teams and cross-functional departments