Iterative Health is hiring for the position of Clinical Research Coordinator I (CRC I) in Mumbai, Maharashtra. The role involves clinical trial coordination, participant recruitment and follow-up, study documentation, clinical data management, and regulatory compliance.
Candidates with a Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, Biotechnology, Allied Health Sciences, or a related scientific discipline, along with 1–3 years of relevant experience, can apply.
Iterative Health Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Iterative Health |
| Job Role | Clinical Research Coordinator I (CRC I) |
| Job Location | Mumbai, Maharashtra, India |
| Salary | ₹12 lakh–₹17 lakh |
| Experience | 1–3 years |
| Qualification | Bachelor’s or Master’s degree in a relevant scientific discipline |
| Employment Area | Clinical Research |
| Travel Requirement | Travel to other sites in India as required |
| Application Mode | Online application |
Positions Available
Clinical Research Coordinator I (CRC I)
The selected candidate will coordinate clinical trial activities, support research participants, maintain study records, and work with investigators, sponsors, CROs, and clinical research teams to ensure quality study execution.
Job Responsibilities
The Clinical Research Coordinator I will be responsible for:
- Coordinating clinical trials according to study protocols, ICH-GCP guidelines, applicable CDSCO regulations, ICMR ethical guidelines, and site SOPs.
- Supporting participant recruitment, pre-screening, enrollment, scheduling, retention, and follow-up.
- Coordinating participant visits and obtaining and documenting informed consent.
- Processing, preparing, and shipping laboratory specimens according to study protocols.
- Maintaining source documents, regulatory files, CTMS updates, and electronic Case Report Forms (eCRFs).
- Entering clinical trial data into EDC systems and resolving data queries.
- Managing investigational product accountability and study supplies.
- Providing operational support across multiple research sites.
- Supporting study startup, site activation, and essential document collection.
- Reviewing study documentation for accuracy, completeness, and protocol compliance.
- Supporting sponsor monitoring visits, audits, and regulatory inspections.
- Collaborating with investigators, sponsors, CROs, central laboratories, and internal teams.
- Ensuring participant safety, data quality, regulatory compliance, and adherence to Good Clinical Practice.
- Participating in ongoing training and quality improvement initiatives.
Eligibility Criteria and Qualifications
Candidates applying for the Clinical Research Coordinator I position should meet the following requirements:
- Educational Qualification: Bachelor’s or Master’s degree in Life Sciences, Pharmacy (B.Pharm/PharmD), Nursing, Biotechnology, Allied Health Sciences, or a related scientific discipline.
- Experience: 1–3 years of clinical research, healthcare, or hospital experience.
- Clinical Research Knowledge: Working knowledge of ICH-GCP guidelines and Indian clinical research regulations.
- Documentation: Understanding of clinical trial documentation and research workflows.
- Multi-site Experience: Experience supporting multiple clinical research sites or working in centralized clinical operations is preferred.
Required Skills
- Clinical trial coordination and clinical operations.
- Knowledge of ICH-GCP and clinical research regulations.
- Clinical trial documentation and data management.
- Familiarity with CTMS, EDC, eSource, EMR/EHR, or similar clinical research systems.
- Proficiency in Microsoft Office applications.
- 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 management skills.
