1,824 Clinical Research Associates jobs in India

Coordinate day-to-day activities of clinical trials from initiation to close-out.

Recruit, screen, and enroll eligible participants as per study protocol.

Schedule and conduct study visits, ensuring adherence to study timelines.

Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other trial-related documents.

Liaise between the sponsor, investigators, ethics committees, and internal teams.

Ensure compliance with ICH-GCP guidelines and regulatory requirements.

Monitor patient safety and report adverse events (AEs/SAEs) promptly.

Support audits and inspections by regulatory authorities or sponsors.

Manage study supplies, including investigational products and lab kits.

Assist in training new clinical staff and support site readiness for future trials.

Certification in clinical research (ACRP, SOCRA, etc.) is an added advantage.

Experience with Electronic Data Capture (EDC) systems.

Familiarity with regulatory submissions and ethics approvals.

Kickstart your career in
Clinical Research
with us

We at
S3 Clinical Research
are looking for
02 passionate interns
in
Ahmedabad
for a
Global Clinical Trial
project.

What's in it for you?

6-month (180 days) structured internship

Internship Certificate to boost your profile

Incentive for top performers

Best performers will be
hired as CRC
at S3 Clinical Research

This is your chance to gain
real-world experience
in global clinical trials and step into a rewarding career in clinical research.

Send your CV to:

We are seeking a dedicated Clinical Research Coordinator to join our growing clinical team. The CRC will support the planning, coordination, and execution of clinical trials according to regulatory guidelines and Good Clinical Practice standards.

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols

Recruit, screen, and enroll study participants while maintaining accurate documentation and records

Required Candidate profile

Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Participant Management: Develop recruitment strategies to identify and enroll eligible participants. Screen potential participants against study inclusion and exclusion criteria. Administer informed consent to explain study procedures, risks, and benefits. Monitor participant health, collect data, and manage any adverse events. Study Operations: Coordinate and conduct all day-to-day activities for the clinical trial. Ensure strict adherence to the study protocol, regulatory guidelines, and Institutional Review Board (IRB) requirements. Collect, process, and ship laboratory specimens. Manage study supplies and equipment. Documentation and Data Management: Maintain comprehensive and organized research documentation, including consent forms, case report forms, and adverse event reports. Collect, manage, and enter accurate study data into databases. Assist with budget preparation and financial tracking for the study. Assist in writing research proposals, reports, and manuscripts.

Job Types: Full-time, Part-time, Fresher

Pay: ₹26, ₹38,275.09 per month

Benefits:

• Provident Fund

Work Location: In person

• Overseeing the trouble-free running of clinical trials
• Collecting data obtained from research, coding and analyzing it
• Managing budgets set aside for research
• Communicating with participants regarding study objectives
• Administering questionnaires and monitoring participants to ensure they adhere to the studys rules
• Liaising with laboratories regarding research findings
• Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards
• Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
• Directing the collection, labeling, storage and transport of all specimens
• Making sure that all equipment and supplies needed for the study are in-stock and in good working order

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life
Responsibilities may include the following and other duties may be assigned.

• Supports clinical studies by executing and maintaining one or more of the following areas.
• Data coordination- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
• Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.
• May process compensation & identify and resolve compensation discrepancies.
• Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
• Assists with periodic audits of clinical study files for completeness and accuracy.

OFFICE SUPPORT CAREER STREAM:
Individual contributors who provide organizational related support or service (administrative or clerical) for other members within the organization. The majority of time is spent in the delivery of support services or activities, typically under supervision.

DIFFERENTIATING FACTORS
Autonomy:
Seasoned individual contributor who provides assistance and training to lower level employees.

Performs a wide variety of non-routine clerical and administrative tasks and may support special projects or assignments.

Works under limited supervision.

Organizational Impact:
Works to deliver day-to-day objectives with significant impact on achievement of results for the job area Work involves obtaining or providing information or data requiring some explanation or interpretation.

Work consists of tasks that are typically not routine.

Innovation and Complexity:
Makes minor changes in systems and processes to solve problems or improve effectiveness of job area .

Expected to independently propose solutions to problems for manager review.

Communication and Influence:
Communicates typically with internal and external contacts .

Obtains and provides information on matters of moderate importance to the job area.

Leadership and Talent Management:
Responsible for providing guidance, coaching and training to other employees within job area.

Required Knowledge and Experience:
Requires broad practical knowledge of operational systems and practices typically gained through extensive experience and/or education.

Requires minimum of 4 years of relevant experience .

Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

About Medtronic
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.

We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here

Company Description

Nuha Hospital provides a wide range of services with world-class facilities tailored to meet the needs of our patients. Our unique, state-of-the-art facilities are spread across the hospital, and each service stands out as a center for excellence. Our dedicated team ensures that every service we offer is delivered with the highest standard of care and expertise.

Role Description

This is a full-time on-site role for a Clinical Research Coordinator, located in Vishakhapatnam. The Clinical Research Coordinator will be responsible for overseeing clinical trials, obtaining informed consent from participants, adhering to research protocols, and maintaining records of the clinical research process. The role involves close collaboration with clinical staff and researchers to ensure compliance and ethical standards are upheld.

Qualifications

• Experience in Clinical Research and Clinical Trials
• Knowledge and practice of obtaining Informed Consent
• Familiarity with Research protocols and regulations
• Strong organizational and record-keeping skills
• Excellent interpersonal and communication skills
• Ability to work on-site in Vishakhapatnam
• Bachelor's degree in a related field; Advanced degrees or certifications in clinical research preferred

Company Description

Vsg Life Sciences is committed to innovation and excellence in the scientific and clinical research fields.

Role Description

This is a full-time on-site role for a Clinical Research Coordinator located in Nashik. The Clinical Research Coordinator will be responsible for managing and overseeing clinical trials and research studies. Day-to-day tasks include obtaining informed consent from participants, ensuring compliance with research protocols, and coordinating the collection, processing, and analysis of research data. The role also involves maintaining accurate study records and liaising with research teams and healthcare providers to ensure the smooth execution of clinical trials.

Qualifications

• Informed Consent and Protocol adherence skills
• Clinical Trials and Clinical Research Experience
• Strong Research skills
• Excellent organizational and communication skills
• Ability to work collaboratively with cross-functional teams
• Bachelor's degree in a related field (e.g., Life Sciences, Nursing, Pharmacy)
• Experience in the clinical research industry is an advantage
• Knowledge of regulatory requirements and ethical standards for clinical trials