Iterative Health is hiring for the position of Clinical Research Coordinator I (CRC I) in Mumbai, Maharashtra. This opportunity is suitable for candidates with a background in Life Sciences, Pharmacy, Nursing, Biotechnology, Allied Health Sciences or a related scientific discipline and 1–3 years of relevant clinical research, healthcare or hospital experience.
The selected candidate will support clinical trial coordination, participant recruitment, informed consent, clinical data management, regulatory documentation and study operations. The role involves working with investigators, sponsors, Contract Research Organisations (CROs), laboratories and research teams to support the safe and compliant execution of clinical studies.
According to the official vacancy listing, the compensation range is ₹12 lakh to ₹17 lakh per year. Candidates should also be willing to travel to other research sites in India when required.
Iterative Health Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company Name | Iterative Health |
| Job Title | Clinical Research Coordinator I |
| Job Code | CRC I |
| Department | Clinical Research / Clinical Operations |
| Job Location | Mumbai, Maharashtra, India |
| Work Mode | Not specified in the listing |
| Employment Type | Not specified in the listing |
| Qualification | Bachelor’s or Master’s degree in a relevant scientific discipline |
| Experience Required | 1–3 years |
| Salary Range | ₹12 lakh–₹17 lakh per year |
| Travel Requirement | Travel to other sites in India when requested |
| Application Mode | Online |
| Official Careers Page | View Iterative Health Jobs |
About Iterative Health
Iterative Health is a healthcare technology and services company focused on accelerating clinical research and improving patient outcomes. The company combines clinical trial expertise with artificial intelligence technology to support research teams and clinical development programmes.
According to the company description in the vacancy listing, its research network includes more than 100 sites across the United States, Europe, India and Australia. Its areas of research include gastrointestinal diseases, hepatology, obesity and cardiology.
The Clinical Research Coordinator I role supports clinical trial activities and participant experience while helping maintain study quality, documentation accuracy and regulatory compliance.
Job Description: Clinical Research Coordinator I
The Clinical Research Coordinator I will assist with the daily operational activities involved in conducting clinical trials. The position requires coordination with research participants, investigators, sponsors, CROs and other stakeholders.
The role includes participant recruitment and scheduling, informed consent documentation, study data entry, specimen handling, regulatory file maintenance and support for monitoring visits and audits.
Candidates should have a good understanding of clinical research workflows, clinical trial documentation and applicable Good Clinical Practice requirements.
Key Responsibilities
1. Clinical Trial Coordination
- Coordinate clinical trial activities according to study protocols and established procedures.
- Support study startup, site activation and the collection of essential study documents.
- Coordinate participant visits and follow-up activities.
- Work with investigators, sponsors, CROs and other research teams to support study execution.
- Assist with operational workflows across multiple research sites.
2. Participant Recruitment and Safety
- Support participant pre-screening, recruitment, enrolment, scheduling and retention.
- Coordinate protocol-required participant visits.
- Obtain and document informed consent according to study requirements and institutional policies.
- Serve as a primary contact for participants throughout their involvement in the study.
- Follow applicable participant safety, privacy and protocol compliance requirements.
3. Clinical Data Management and Documentation
- Maintain accurate and timely source documentation and regulatory records.
- Update Clinical Trial Management System (CTMS) records.
- Enter clinical trial data into Electronic Data Capture (EDC) systems.
- Maintain electronic Case Report Forms (eCRFs).
- Assist with resolving data queries within required timelines.
- Review study documentation for completeness, accuracy and protocol compliance.
4. Laboratory Specimen and Study Supply Management
- Process, prepare and ship laboratory specimens according to study protocols and laboratory guidelines.
- Coordinate investigational product accountability.
- Support study supply management and related documentation.
- Follow the applicable procedures for handling study materials.
5. Regulatory Compliance and Quality Assurance
- Follow ICH-GCP guidelines, applicable CDSCO regulations, ICMR ethical guidelines and site Standard Operating Procedures (SOPs).
- Maintain essential study documents throughout the clinical trial lifecycle.
- Prepare for and support sponsor monitoring visits, audits and regulatory inspections.
- Help maintain data quality and inspection readiness.
- Participate in training and quality improvement activities.
6. Collaboration and Site Support
- Coordinate with local research site teams and central clinical operations.
- Support documentation, participant scheduling and data management across assigned sites.
- Communicate with investigators, sponsors, CROs and central laboratories.
- Travel to other research sites in India when requested.
Eligibility Criteria and Educational Qualifications
Candidates should meet the educational and experience requirements outlined in the vacancy.
| Requirement | Details |
|---|---|
| Educational Qualification | Bachelor’s or Master’s degree |
| Preferred Disciplines | Life Sciences, Pharmacy, B.Pharm, PharmD, Nursing, Biotechnology, Allied Health Sciences or a related scientific field |
| Experience | 1–3 years in clinical research, healthcare or a hospital environment |
| Clinical Research Knowledge | Working knowledge of ICH-GCP and Indian clinical research regulations |
| Documentation | Understanding of clinical trial documentation and research workflows |
| Communication | Strong written and verbal communication skills in English |
| Computer Skills | Proficiency in Microsoft Office |
| Preferred Technical Knowledge | CTMS, EDC, eSource, EMR/EHR or similar clinical research systems |
| Multi-Site Experience | Preferred, particularly in centralized clinical operations |
Experience supporting multiple research sites or working in a centralized clinical operations environment is an advantage, according to the listing.
Skills Required for the CRC I Position
Candidates interested in this role should demonstrate the following skills:
- Clinical trial coordination and organisational ability.
- Understanding of clinical research documentation.
- Knowledge of ICH-GCP and applicable Indian clinical research requirements.
- Strong attention to detail and data accuracy.
- Participant communication and interpersonal skills.
- Ability to manage multiple studies and competing priorities.
- Familiarity with clinical research databases and electronic systems.
- Teamwork and coordination with internal and external stakeholders.
- Effective written and spoken English.
- Willingness to travel to research sites when required.
Physical Requirements
The official listing mentions the following physical requirements:
- Ability to sit, stand and move around clinical and office environments for extended periods.
- Ability to lift and move items weighing up to 10 kilograms (22 pounds) when necessary.
Candidates should review these requirements when assessing their suitability for the position.
Salary for Iterative Health Clinical Research Coordinator I
The official vacancy listing specifies a compensation range of ₹12,00,000 to ₹17,00,000 per year.
| Salary Particular | Details |
|---|---|
| Minimum Listed Compensation | ₹12 LPA |
| Maximum Listed Compensation | ₹17 LPA |
| Exact Salary Structure | Not specified |
| Additional Benefits | Not detailed in the available listing |
The final offer may depend on the employer’s compensation structure, the candidate’s experience and other relevant factors. Applicants should confirm whether the quoted range represents fixed pay, total compensation or another salary structure directly with the recruitment team.
How to Apply for Iterative Health Recruitment 2026
Eligible candidates can apply through Iterative Health’s official careers portal.
Position: Clinical Research Coordinator I – India
Location: Mumbai, India
Candidates should locate the Clinical Research Coordinator I – India opening and complete the application using the instructions on the official job page.
Before applying, prepare an updated CV highlighting your educational qualifications, clinical research or healthcare experience, ICH-GCP knowledge, documentation skills and familiarity with clinical research systems.
For accessibility accommodations during the application or interview process, the company lists the following contact email: CandidateAccommodations@iterative.health.
Frequently Asked Questions (FAQs)
1. Is Iterative Health hiring Clinical Research Coordinators in 2026?
The company’s careers listing includes the Clinical Research Coordinator I – India position in Mumbai.
2. What is the job location?
The position is based in Mumbai, Maharashtra, India.
3. What is the salary for Clinical Research Coordinator I at Iterative Health?
The listed compensation range is ₹12 lakh to ₹17 lakh per year. Candidates should confirm the final salary structure with the employer.
4. What qualification is required?
A bachelor’s or master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Allied Health Sciences or a related scientific discipline is listed.
5. How much experience is required?
The vacancy specifies 1–3 years of clinical research, healthcare or hospital experience.
6. Can B.Pharm and PharmD candidates apply?
Yes. Pharmacy, including B.Pharm and PharmD, is among the educational backgrounds specified in the listing, provided candidates also meet the relevant experience and other requirements.
7. Is ICH-GCP knowledge required?
Yes. The listing asks for working knowledge of ICH-GCP guidelines and Indian clinical research regulations.
8. Is travel required for this role?
Candidates must be willing to travel to other research sites in India upon request.
9. What are the main responsibilities?
The role includes clinical trial coordination, participant recruitment and follow-up, informed consent, data entry, documentation, specimen handling, regulatory compliance and support for audits and monitoring visits.
10. How can candidates apply?
Candidates can visit the official Iterative Health careers portal and locate the Clinical Research Coordinator I – India vacancy.
Disclaimer
This article is based on the information provided in Iterative Health’s official job listing. Compensation, eligibility criteria, responsibilities and vacancy status may change. Candidates should review the official job page and confirm the latest details before submitting their applications.