559 Research Coordinator jobs in India

• Recruit, screen, and enroll eligible participants for clinical trials according to protocol requirements.
• Conduct informed consent process and ensure participant understanding.
• Manage study documentation, including case report forms (CRFs), source documents, and regulatory binders.
• Administer study medications and conduct study procedures as per protocol.
• Monitor participants for adverse events and report them appropriately.
• Collect, manage, and ensure the accuracy and completeness of study data.
• Liaise with principal investigators, study sponsors, ethics committees, and regulatory agencies.
• Coordinate study visits and ensure timely completion of all protocol-related procedures.
• Maintain effective communication with participants and their families.
• Participate in study-related training and meetings.
• Adhere to Good Clinical Practice (GCP) guidelines and institutional policies.
• Manage study supplies and equipment.

• Bachelor's degree in a life science, nursing, or a related field.
• Minimum of 3-5 years of experience as a Clinical Research Coordinator or similar role.
• Strong understanding of clinical trial processes, GCP, and regulatory requirements (e.g., ICMR, FDA).
• Excellent organizational, time management, and multitasking skills.
• Proficiency in clinical data management systems and electronic data capture (EDC) tools.
• Exceptional interpersonal and communication skills, with the ability to build rapport with diverse patient populations.
• Attention to detail and commitment to maintaining data integrity.
• Ability to work effectively in a hybrid environment, balancing remote and on-site duties.
• Familiarity with the healthcare landscape in **Kochi, Kerala, IN** is an advantage.

• Coordinating and managing all aspects of assigned clinical trials.
• Recruiting, screening, and consenting study participants according to protocol guidelines.
• Collecting, documenting, and reporting clinical data accurately and efficiently.
• Ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
• Monitoring participant adherence to treatment plans and study procedures.
• Scheduling participant visits and managing study-related appointments.
• Maintaining accurate and organized study documentation and regulatory binders.
• Liaising with investigators, study sponsors, and other stakeholders.
• Administering study medications or investigational products as per protocol.
• Responding to participant queries and providing appropriate support.

• Bachelor's degree in Nursing, Pharmacy, Life Sciences, or a related healthcare field.
• Previous experience as a Clinical Research Coordinator or in a similar role within clinical research.
• In-depth knowledge of clinical trial phases, protocols, and regulatory requirements (e.g., GCP, ICH guidelines).
• Excellent patient interaction and communication skills.
• Strong organizational abilities and meticulous attention to detail.
• Proficiency in using electronic data capture (EDC) systems and clinical trial management software.
• Ability to work independently and as part of a multidisciplinary team.
• Certified Clinical Research Professional (CCRC) or similar certification is a plus.
• Strong understanding of medical terminology and disease processes.
• Commitment to patient confidentiality and ethical research conduct.

• Assist in the planning, implementation, and coordination of clinical research studies.
• Recruit, screen, and enroll study participants according to protocol guidelines.
• Obtain informed consent from participants and ensure their rights and well-being are protected.
• Collect, manage, and accurately document study data, ensuring data integrity and confidentiality.
• Schedule and coordinate participant visits, laboratory tests, and medical procedures.
• Monitor participants for adverse events and report them promptly as required.
• Maintain study regulatory binders and essential documents in an organized and up-to-date manner.
• Liaise with investigators, research staff, sponsors, and regulatory agencies.
• Prepare and submit study-related reports and documentation.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and other applicable regulations.
• Assist in the preparation for site visits and audits by regulatory authorities or sponsors.
• Provide support to principal investigators and other research team members.
• Manage study supplies and equipment, ensuring availability and proper functioning.
• Conduct remote follow-up with participants as necessary.

• Bachelor's degree in a life science, nursing, or a related field.
• Minimum of 3 years of experience in clinical research coordination.
• Thorough knowledge of clinical trial processes, GCP, and regulatory requirements (e.g., ICH).
• Experience with electronic data capture (EDC) systems and other research software.
• Excellent organizational, time management, and multitasking skills.
• Strong written and verbal communication abilities.
• Ability to work independently and as part of a remote team.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• High level of attention to detail and accuracy.
• Professional demeanor and ethical conduct.

• Recruit, screen, and enroll eligible participants for clinical trials.
• Obtain informed consent from study participants.
• Schedule and coordinate study visits, including assessments and procedures.
• Collect, record, and manage study data accurately and efficiently, ensuring data integrity.
• Administer study-related tests and procedures as per protocol.
• Monitor participants for adverse events and report them promptly.
• Maintain regulatory files and study documentation in compliance with GCP and regulatory requirements.
• Communicate effectively with investigators, study sponsors, and other stakeholders.
• Manage study supplies and equipment.
• Assist with site initiation, monitoring visits, and close-out activities.

• Bachelor's degree in Nursing, Life Sciences, Pharmacy, or a related healthcare field.
• Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar clinical research role.
• Thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Proficiency in electronic data capture (EDC) systems and clinical trial management software.
• Excellent organizational, time management, and multitasking abilities.
• Strong written and verbal communication skills.
• Attention to detail and commitment to accuracy.
• Ability to work effectively in a fast-paced, clinical research environment.
• Certification from a recognized professional body (e.g., ACRP, SoCRA) is a plus.

Clinical Research Coordinator (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 Coordinators.

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

If youre 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

• Coordinate and manage multiple clinical research studies simultaneously, ensuring adherence to protocols and regulations.
• Oversee participant recruitment, screening, enrollment, and follow-up processes.
• Ensure accurate and timely collection, management, and documentation of research data using EDC systems.
• Liaise effectively with principal investigators, study sponsors, and regulatory bodies.
• Maintain study files, regulatory binders, and essential documents according to GCP guidelines.
• Monitor study progress, identify potential issues, and implement corrective actions.
• Educate participants about study procedures, risks, and benefits.
• Assist with the preparation of study-related reports, manuscripts, and presentations.
• Ensure compliance with all Institutional Review Board (IRB) and ethical guidelines.
• Manage study budgets and track expenditures.
• Contribute to the development of new research protocols and study designs.
• Provide mentorship and guidance to junior research staff as needed.

• Bachelor's degree in a health-related science field (e.g., Nursing, Public Health, Biology). Master’s degree preferred.
• Minimum of 5 years of experience in clinical research coordination.
• Proven experience managing multiple clinical trials from initiation to close-out.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements.
• Proficiency with Electronic Data Capture (EDC) systems and other research software.
• Excellent organizational, time management, and problem-solving skills.
• Exceptional interpersonal and communication skills.
• Ability to work independently and collaboratively in a remote setting.
• Experience in community-based research or public health initiatives is a plus.
• Current certifications such as CRA or CCRP are highly desirable.

• Coordinate and manage all aspects of assigned clinical trials, from initiation to closeout.
• Recruit, screen, and enroll eligible participants, ensuring informed consent procedures are thoroughly followed.
• Schedule and conduct study visits, administering study-related procedures and collecting data accurately.
• Maintain detailed and accurate study records, including source documents, case report forms (CRFs), and regulatory binders.
• Monitor participant adherence to study protocols and manage adverse event reporting according to established guidelines.
• Liaise with investigators, sponsors, ethics committees, and regulatory authorities to ensure compliance and smooth trial operation.
• Manage investigational product accountability and distribution as per protocol.
• Prepare for and host monitoring visits, regulatory inspections, and audits, ensuring all documentation is readily available and accurate.
• Assist in the development of study protocols, informed consent forms, and other research-related documents.
• Provide training and mentorship to junior research staff and study volunteers.

• Bachelor's degree in Nursing, Life Sciences, or a related healthcare field.
• Minimum of 5 years of experience as a Clinical Research Coordinator, with demonstrated experience in managing complex trials.
• In-depth knowledge of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements (e.g., FDA, ICH).
• Proven experience in participant recruitment, screening, and informed consent processes.
• Strong understanding of medical terminology and clinical procedures.
• Excellent organizational, time management, and multitasking skills.
• Proficiency in electronic data capture (EDC) systems and clinical trial management software (CTMS).
• Exceptional attention to detail and commitment to data accuracy and integrity.
• Strong interpersonal and communication skills, with the ability to interact effectively with participants, investigators, and sponsors.
• Ability to work effectively in a fast-paced, team-oriented environment.

• Coordinate and manage all aspects of clinical research studies from initiation to closure.
• Recruit, screen, and enroll eligible participants according to study protocols.
• Educate participants about study procedures, risks, and benefits, ensuring informed consent is obtained.
• Administer study-related assessments, collect data accurately, and maintain detailed participant records.
• Monitor participants’ progress and report any adverse events or deviations from the protocol.
• Liaise with principal investigators, study sponsors, regulatory agencies, and other healthcare professionals.
• Ensure compliance with all applicable regulations, including GCP (Good Clinical Practice), FDA guidelines, and institutional policies.
• Manage study supplies, equipment, and laboratory samples.
• Assist with study site visits, audits, and inspections.
• Contribute to the development of study protocols and informed consent forms.
• Maintain study documentation and ensure its completeness and accuracy.
• Process and analyze research data, preparing reports as required.
• Support the ethical conduct of research and protect participant confidentiality.
• Participate in ongoing training and professional development related to clinical research.

• Bachelor's degree in Nursing, Life Sciences, Public Health, or a related field. A Master's degree is preferred.
• Minimum of 4 years of experience as a Clinical Research Coordinator or in a similar research role.
• Strong knowledge of clinical trial phases, research methodologies, and regulatory requirements (GCP, FDA).
• Experience with electronic data capture (EDC) systems and electronic health records (EHR).
• Excellent organizational, time management, and multitasking skills.
• Proficiency in data collection, management, and analysis.
• Exceptional communication, interpersonal, and patient-advocacy skills.
• Ability to work independently with minimal supervision in a remote setting.
• Certification as a Certified Clinical Research Professional (CCRC) or similar is a plus.
• Proficiency in Microsoft Office Suite and statistical software.

• Coordinate all study-related activities at the clinical site, ensuring compliance with protocols, SOPs, and regulatory guidelines (GCP, ICH).
• Recruit, screen, and enroll eligible participants into clinical trials.
• Educate participants about the study protocol, obtain informed consent, and answer participant queries.
• Schedule and conduct participant visits, administer study procedures, and collect data accurately.
• Manage study documentation, including source documents, case report forms (CRFs), and investigational product accountability.
• Monitor participant safety, report adverse events and serious adverse events in a timely manner.
• Collaborate effectively with investigators, study sponsors, Contract Research Organizations (CROs), and regulatory agencies.
• Maintain communication with participants throughout the study duration.
• Participate in study initiation visits, monitoring visits, and close-out visits.
• Ensure the security and confidentiality of all study-related data and participant information.
• Order, manage, and maintain study supplies and equipment.
• Assist in preparing for and hosting site audits and regulatory inspections.
• Contribute to the development and review of study-related documents and materials.
• Mentor and support junior research staff and provide training as needed.

• Bachelor's degree in Nursing, Life Sciences, Pharmacy, or a related healthcare field.
• Minimum of 5 years of experience as a Clinical Research Coordinator in an academic, hospital, or industry setting.
• In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Proven experience in patient recruitment, informed consent process, and data collection.
• Strong understanding of medical terminology and clinical trial procedures.
• Excellent organizational, time management, and multitasking skills.
• Proficiency in electronic data capture (EDC) systems and clinical trial management software (CTMS).
• Exceptional communication, interpersonal, and problem-solving abilities.
• Ability to work independently and as part of a collaborative team.
• Relevant certifications (e.g., ACRP, SoCRA) are a significant advantage.
• Experience with specific therapeutic areas is a plus.