1,694 Clinical Research Associates jobs in India

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

JOB SUMMARY:

The Clinical Research Coordinator manages and supports clinical research studies by coordinating protocols, overseeing data collection, assisting investigators, and ensuring regulatory compliance. The role involves working closely with research staff and participants to ensure smooth day-to-day operations and successful study execution.

JOB DESCRIPTION:

• Plans and coordinates the initiation of the research study protocol, and ensuring adherence to operating policies and procedures.
• Plans, implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data.
• Coordinates research subjects and/or volunteers, as appropriate to specific study objectives and work scope.
• Ensures the smooth and efficient day-to-day operation of research and data collection activities.
• Coordinates the day-to-day activities of any technical support staff.
• Coordinates the provision of support services to investigators and researchers.
• Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, administrators, sponsors/CRO, and/or regulatory bodies.
• To participate in clinical floor activities on an ongoing basis with research staff to ensure adequate clinical support for trial activities.
• To perform miscellaneous job-related duties as assigned.

Qualifications & Experience:

• B. Pharm, M. Pharm, Pharm. D, M.Sc(Life Sciences), B. Tech (Biotechnology), M.Teh (Biotechnology), B.Sc(Nursing), M.Sc(Nursing), Msc.Microbiology, Msc.Zoology
• Fluent English Communication

Benefits:

• Hostel facility available for female candidates
• Leave encashment
• Paid sick time
• ESI

Schedule:

• Day shift (9.00 Am to 6.00 Pm)

Preferred Female Candidates

Fresher / Experience (0 to 2 Years)

Pay:

• · ₹15, ₹6,600.00 per month

Contact Details: ,

Job Types: Full-time, Permanent

Pay: , ,600.00 per month

Benefits:

• Leave encashment
• Paid sick time
• Provident Fund

Education:

• Master's (Required)

Work Location: In person

About the Job

We are looking for passionate Clinical Research Coordinators (CRC) to join our growing team. This is an exciting opportunity for fresh graduates with a clinical research course or background in life sciences/pharmacy who want to build a career in clinical trials and research.

Position Details

Role: Clinical Research Coordinator

Location: Delhi

Employment Type : Full-time

Experience: Freshers with clinical research training or related background encouraged to apply!

Key Responsibilities

• Conduct clinical trials in compliance with ICH GCP and protocol guidelines.
• Support study start-up activities and assist with site initiation.
• Participate in recruitment and retention of study subjects.
• Complete and maintain source documents, CRFs, and logs accurately.
• Compile and update the Site Master File.
• Manage Investigational Products (IP), including accountability and shipping.
• Coordinate submissions and communication with the Ethics Committee.
• Update sponsors on study progress and prepare for monitoring visits.
• Perform other responsibilities assigned by management.

Who Can Apply

• Freshers with a completed Clinical Research course.
• Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields.
• Strong interest in clinical trials and regulatory compliance.
• Excellent organisational, communication, and documentation skills.

Why Join Us?

Gain hands-on experience in clinical trials.

Learn directly from experienced professionals.

Be part of innovative projects that shape the future of healthcare.

A great opportunity to grow your career in clinical research.

• 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

Educational qualification: B-Pharm /M-Pharm

Salary :15k

Both male and female are OK

Both freshers and experienced are OK

Job Summary:

Seeking a dedicated and organized Research Coordinator to support the Research Department at Jothydev's Diabetes Research Centre. This role involves coordinating various ongoing research projects, ensuring smooth project management, and facilitating communication between team members. The ideal candidate will be a recent MSc graduate with strong communication skills and a keen interest in research activities. Freshers are encouraged to apply

Job Description:-

Assist in trial management and site coordination.

Maintain Trial Master Files (TMF) and ensure proper documentation and Regulatory documentation.

Ability to maintain drug storage Drug dispensing and accountability.

Support in patient enrollment and clinical trial material logistics.

schedule meetings, prepare agendas and minutes Technical & Soft Skills

Knowledge of ICH- GCP guidelines

Proficiency in Microsoft office & Clinical trial software

Strong organizational & Communication skills- Multitasking

Qualifications:

B-Pharm/ M Pharm

Excellent verbal and written communication skills.

Strong organizational and multitasking abilities.

Genuine interest in research activities and enthusiasm for learning.

Job Types: Full-time, Fresher

Pay: ₹15,000.00 per month

Work Location: In person

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

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

About Us:

Kairos R and D Solutions Pvt. Ltd. is a fast-growing Clinical Trials Organization based in Hyderabad, dedicated to providing high-quality, ethical, and efficient clinical trial services. We are committed to excellence in research and uphold the highest standards of regulatory compliance and data integrity.

Job Description:

We are seeking a dedicated and experienced
Clinical Research Coordinator (CRC)
to join our dynamic team in Hyderabad. The ideal candidate will have a strong understanding of clinical trial processes, GCP guidelines, and sponsor protocols, with at least one year of hands-on experience coordinating clinical trials.

Key Responsibilities:

• Coordinate and manage day-to-day clinical trial activities at the site.
• Ensure compliance with study protocols, ICH-GCP, and applicable regulatory requirements.
• Manage subject recruitment, informed consent process, screening, enrollment, and follow-up visits.
• Collect and enter accurate source data and case report forms (CRFs) in a timely manner.
• Act as a primary liaison between the site, sponsors, and monitors.
• Prepare for and support monitoring visits, audits, and regulatory inspections.
• Maintain and organize study documentation (ISF, logs, accountability records, etc.).
• Train and mentor junior coordinators as needed.

Qualifications & Skills:

• Bachelor's degree in life sciences, pharmacy, nursing, or a related field.
• Minimum of 1 years of experience coordinating clinical trials.
• Strong knowledge of ICH-GCP, Indian regulatory requirements, and ethical guidelines.
• Excellent organizational and communication skills.
• Proficient in Microsoft Office and electronic data capture (EDC) systems.
• Ability to work independently and handle multiple tasks efficiently.

What We Offer:

• A collaborative and supportive work environment.
• Opportunities for professional growth and training.
• Competitive salary and performance-based incentives.
• Exposure to a diverse portfolio of clinical studies.

Designation : Clinical Research Coordinator

1. Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

2. Working closely with the PI ,CRC participates in an integral way in the informed consent process by communicating with the potential study subjects about protocol. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol in order to be able to answer all questions pertaining to the study posed during the informed consent process.

3. Coordinates approval of new study aggrements and contracts.

4. Coordinates and attends sponsor Site Selection visits, Routine monitoring visits, and study close out visits.

5. Responds to data clarification requests in a timely manner.

6. Coordinates with PIs and departments to help ensure that clinical research and related activities are performed in accordance with protocol , SOP,GCP and applicable regulatory requirement.

7.Maintains subjects screening logs and protocol deviation logs.

8.Maintains excel sheet, tracking updates to database of all subjects enrolled on clinical trials.

1. Coordinates and Facilitates monitoring and auditing visits.

2. Collaborates with PI and institution to respond to any Audit findings and implement approved recommendations.

3. Establishes and organizes study files, including but not limited .

Location - Kolkata

Full Time , ON site

Only Freshers can apply

Qualifications required: BSc,Msc, Bpharm

Immediate Joining.

Interested candidates send resume in mail id