Vashi Navi Mumbai Maharashtra Clinical research Jobs – 99 Open Jobs Today

Clinical Research Coordinator I - India
Iterative Health —Mumbai, Maharashtra
- ₹12,00,000 - ₹17,00,000 a year
- English
- Research
- Microsoft Office
Quick apply
Clinical Research - Infection control
Thermaissance —Mumbai, Maharashtra
- ₹50,000 - ₹70,000 a month
- Part-time
- Medicine
- B.Sc
- Master's degree
Quick apply
12d
Clinical Project Coordinator - Entry
Medpace, Inc. —Navi Mumbai, Maharashtra
- Full-time
- Bachelor's degree
- Health insurance
- Paid time off
14d
Clinical Pharmacologist
HRDR —Mumbai, Maharashtra
- ₹4,00,000 - ₹7,00,000 a month
- Full-time
- Medicine
- Doctoral degree
- In-person
Quick apply
Head Quality Assurance-Clinical Research
Expecto Health Science —Kharghar, Navi Mumbai, Maharashtra
- ₹8,00,000 - ₹20,00,000 a year
- Full-time
- Management
- Research
- Master's degree
- Health insurance
- Paid time off
Quick apply
14d
Clinical Pharmacologist
White lotus international Hospital —Navi Mumbai, Maharashtra
- ₹30,000 - ₹55,000 a month
- Full-time
- Medicine
- ICU experience
- Analysis skills
Quick apply
Clinical Trial Coordinator - (FSP )
Thermo Fisher Scientific —Mumbai, Maharashtra
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
Medical Affairs Executive
Clini launch Research Institute —Andheri, Mumbai, Maharashtra
- ₹50,000 - ₹80,000 a month
- Full-time
- Research
- Analysis skills
- Presentation skills
- Health insurance
- Paid time off
Quick apply
12d
Clinical Research Medical Advisor
Novartis —Mumbai, Maharashtra
- Full-time
- Medicine
- Doctoral degree
- Bachelor's degree
7d
Clinical Psychologist
MOC CANCER CARE & RESEARCH CENTRE —Panvel, Maharashtra
- ₹20,000 - ₹28,000 a month
- Full-time
- English
- Microsoft Office
- Master's degree
- Health insurance
- Life insurance
Quick apply
1d
Research Scientist-ADL
Piramal Pharma Limited —Navi Mumbai, Maharashtra
- Full-time
- APIs
9d
Randomization & Study Product Coordinator
Medpace, Inc. —Navi Mumbai, Maharashtra
- Full-time
- Microsoft Excel
- Bachelor's degree
- Health insurance
- Paid time off
Clinical Data Svs Associate
Accenture —Mumbai, Maharashtra
- Full-time
- Master's degree
- Bachelor's degree
Resident Medical Officer (RMO)
SHUSHRUSHA CITIZENS' CO-OPERATIVE HOSPITAL LIMITED —Mumbai, Maharashtra
- ₹22,000 - ₹55,000 a month
- Weekend availability
- Bachelor's degree
- Patient care
- In-person
- Flexible schedule
- Food provided
Quick apply
Deputy Director -Complementary and Alternative Medicine (CAM)
Indian Cancer Society, Mumbai —Parel, Mumbai, Maharashtra
- ₹1,00,000 - ₹1,25,000 a month
- Full-time
- Up to 50% travel
- Master's degree
- Business development
- Paid sick time
Quick apply
Regeneration Specialist
Research ayu —Kalyan-Dombivli, Maharashtra
- From ₹25,000 a month
- Anatomy knowledge
- Bachelor's degree
- In-person
- Health insurance
- Paid sick time
Quick apply
8d
Resident Medical Officer (RMO)
Surana Hospital & Research Centre —Mumbai, Maharashtra
- ₹20,834.00 - ₹77,259.93 a month
- Full-time
- Bachelor's degree
- Patient care
- In-person
Quick apply
Regulatory Submissions Coordinator (Senior/ Experienced)
Medpace, Inc. —Navi Mumbai, Maharashtra
- Full-time
- Research
- Bachelor's degree
- Communication skills
- Health insurance
- Paid time off
TL-Medical Safety
Cognizant —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Research
- Analysis skills
- Travel
- Health insurance
Hospital Administrator
Shree Pragati Foundations Hira Mongi Navneet Hospital & Research Centre —Mulund West, Mumbai, Maharashtra
- From ₹35,000 a month
- Full-time
- Microsoft Word
- English
- Microsoft Office
Quick apply

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Clinical Research Coordinator I - India

Iterative Health -
Mumbai, Maharashtra

Quick apply

Job details

₹12,00,000 - ₹17,00,000 a year

Qualifications

Clinical research
English
Research
Microsoft Office
Master's degree
Bachelor's degree
Organisational skills
EMR systems
Pharmacy
Clinical trials
Interviewing
Communication skills
Hospital experience

Full job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

As a Clinical Research Coordinator I (CRC I) at Iterative Health India, you will play an integral role in the successful execution of clinical trials while ensuring an exceptional participant experience. You will support the day-to-day coordination of research studies by partnering with investigators, sponsors, CROs, and cross-functional teams to deliver high-quality clinical research that advances innovative therapies.

This position requires strong organizational skills, attention to detail, and a commitment to participant safety, protocol compliance, and research excellence.

Location: Mumbai, India

Compensation: ₹12 lakh- ₹17 lakh

Travel: Willingness to travel to other sites in India upon request.

Where You'll Drive Impact

Coordinate and execute clinical trial activities in accordance with study protocols, ICH-GCP guidelines, applicable CDSCO regulations, ICMR ethical guidelines, and site SOPs.
Support participant recruitment, pre-screening, enrollment, scheduling, retention, and follow-up activities.
Provide centralized operational support across multiple research sites, coordinating study documentation, participant scheduling, data management activities, and operational workflows while partnering with local site teams to ensure consistent study execution and regulatory compliance.
Coordinate and conduct protocol-required participant visits while ensuring participant safety and protocol compliance.
Obtain and document informed consent in accordance with study requirements and institutional policies.
Process, prepare, and ship laboratory specimens according to protocol requirements and laboratory guidelines.
Maintain accurate, complete, and timely source documentation, regulatory documentation, CTMS updates, and electronic Case Report Forms (eCRFs).
Enter study data into EDC systems and assist with timely resolution of data queries.
Coordinate investigational product accountability and study supply management.
Serve as the primary point of contact for study participants throughout study participation.
Collaborate with investigators, sponsors, CROs, central laboratories, and internal teams to ensure successful study execution.
Support study startup, site activation, document collection, and ongoing maintenance of essential study documentation across assigned research sites.
Review study documentation for completeness, accuracy, and protocol compliance while supporting data quality and inspection readiness.
Prepare for and support sponsor monitoring visits, audits, and regulatory inspections.
Maintain study regulatory files and essential documents throughout the study lifecycle.
Ensure compliance with applicable regulations, institutional policies, privacy requirements, and Good Clinical Practice (ICH-GCP).
Participate in ongoing training and quality improvement initiatives.
Willingness to travel to other sites in India upon request.
Perform other duties as assigned.

What You Bring to the Team

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 clinical research, healthcare, or hospital experience.
Working knowledge of ICH-GCP guidelines and Indian clinical research regulations.
Experience supporting multiple clinical research sites or working in a centralized clinical operations environment is preferred.
Strong understanding of clinical trial documentation and research workflows.
Excellent organizational skills with strong attention to detail.
Ability to manage multiple studies and competing priorities in a fast-paced environment.
Effective verbal and written communication skills in English.
Strong interpersonal skills with the ability to build relationships with participants, investigators, sponsors, and internal stakeholders.
Proficiency with Microsoft Office applications.
Familiarity with clinical research technologies, including CTMS, EDC, eSource, EMR/EHR, or similar systems preferred

Physical Requirements

Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
Ability to lift and move up to 10 kilograms (22 pounds) as needed

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

Quick apply

Refine Your Search

clinical research jobs in vashi navi mumbai maharashtra

Clinical Research Coordinator I - India

Clinical Research - Infection control

Clinical Project Coordinator - Entry

Clinical Pharmacologist

Head Quality Assurance-Clinical Research

Clinical Pharmacologist

Clinical Trial Coordinator - (FSP )

Medical Affairs Executive

Clinical Research Medical Advisor

Clinical Psychologist

Research Scientist-ADL

Randomization & Study Product Coordinator

Clinical Data Svs Associate

Resident Medical Officer (RMO)

Deputy Director -Complementary and Alternative Medicine (CAM)

Regeneration Specialist

Resident Medical Officer (RMO)

Regulatory Submissions Coordinator (Senior/ Experienced)

TL-Medical Safety

Hospital Administrator

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