Iterative Health is hiring for the position of Clinical Research Coordinator II – India in Mumbai, Maharashtra. The role focuses on clinical trial coordination, participant management, clinical research documentation, data quality, and regulatory compliance. Candidates with a background in Pharmacy, Life Sciences, Nursing, Biotechnology, or related scientific disciplines and 1–3 years of relevant experience can apply.
The position offers a compensation range of ₹15 lakh to ₹25 lakh and requires a willingness to travel to other research sites in India when requested.
Job Details
| Particulars | Details |
|---|---|
| Company | Iterative Health |
| Job Role | Clinical Research Coordinator II – India |
| Job Location | Mumbai, Maharashtra, India |
| Qualification | Bachelor’s or Master’s degree in a relevant scientific discipline |
| Experience | 1–3 years |
| Salary | ₹15 lakh–₹25 lakh |
| Employment Type | Full-time |
| Travel Requirement | Travel to other sites in India upon request |
| Application Mode | Online application |
| Official Job Portal | Apply at Iterative Health |
Positions Available
Clinical Research Coordinator II – India
The selected candidate will coordinate clinical trial activities, support participant visits, maintain study documentation, update clinical trial systems, and work with investigators, sponsors, CROs, laboratories, and research site teams.
Responsibilities
- Coordinate clinical trial activities according to study protocols, ICH-GCP guidelines, CDSCO regulations, ICMR ethical guidelines, and site SOPs.
- Support participant recruitment, pre-screening, enrollment, scheduling, retention, and follow-up.
- Coordinate research operations and documentation across multiple clinical research sites.
- Conduct protocol-required participant visits and obtain and document informed consent.
- Process, prepare, and ship laboratory specimens according to study requirements.
- Maintain source documents, regulatory files, CTMS records, and electronic Case Report Forms (eCRFs).
- Enter clinical trial data into EDC systems and help resolve data queries.
- Manage investigational product accountability and study supplies.
- Coordinate with investigators, sponsors, CROs, central laboratories, and internal teams.
- Support study startup, site activation, essential document collection, and ongoing study maintenance.
- Review documentation for accuracy, completeness, and protocol compliance.
- Support sponsor monitoring visits, audits, and regulatory inspections.
- Maintain participant communication throughout the study and follow applicable privacy and regulatory requirements.
Eligibility and Qualifications
Candidates should meet the following requirements:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy (B.Pharm/PharmD), Nursing, Biotechnology, Allied Health Sciences, or a related scientific discipline.
- 1–3 years of experience in clinical research, healthcare, or a hospital environment.
- Working knowledge of ICH-GCP guidelines and Indian clinical research regulations.
- Understanding of clinical trial documentation and research workflows.
- Willingness to travel to other research sites in India when required.
Experience supporting multiple clinical research sites or working in centralized clinical operations is preferred.
Required Skills
- Clinical trial coordination and operational support.
- Clinical research documentation and regulatory compliance.
- Knowledge of ICH-GCP and Indian clinical research regulations.
- Familiarity with CTMS, EDC, eSource, EMR/EHR, or similar clinical research systems.
- Strong organizational skills and attention to detail.
- Ability to manage multiple studies and competing priorities.
- Effective written and verbal communication skills in English.
- Strong interpersonal and stakeholder coordination skills.
- Proficiency in Microsoft Office applications.
