Medpace Clinical Research India is hiring for the position of Clinical Research Associate Entry (CRA Entry) in Navi Mumbai, Maharashtra. This is a full-time, permanent opportunity within the Research & Development function for candidates looking to begin or develop a career in clinical research.
The position is suitable for graduates from healthcare and life science backgrounds. No prior clinical research experience is required, as Medpace provides initial and ongoing training through its PACE® CRA Training Program.
The role involves clinical trial site visits, source data verification, regulatory document review, investigational product or medical device accountability, adverse event review, site monitoring and preparation of monitoring reports.
Medpace Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Medpace Clinical Research India |
| Position | Clinical Research Associate Entry |
| Department | Research & Development |
| Job Location | Navi Mumbai, Maharashtra |
| Employment Type | Full-time, Permanent |
| Experience | 0–1 years |
| Qualification | Minimum Bachelor’s Degree |
| Preferred Background | Health or Life Science-related field |
| Work Area | Clinical Research |
| Travel Requirement | Approximately 60–80% nationally |
| Application Mode | Online |
About Medpace
Medpace is a full-service Contract Research Organization (CRO) that provides clinical development services to biotechnology, pharmaceutical and medical device companies.
The organization supports clinical development programs across different therapeutic areas, including oncology, cardiology, metabolic and endocrinology, central nervous system, and anti-viral and anti-infective areas.
Medpace operates internationally and provides opportunities for professionals to work with physicians, scientists and other clinical research specialists.
About the Clinical Research Associate Entry Role
The Clinical Research Associate Entry position is designed for candidates entering the CRA profession. Medpace states that candidates can come from a variety of medical and science-related healthcare backgrounds.
Examples of backgrounds represented among successful CRA candidates include nursing, dietetics, pharmacy-related roles, pharmaceutical or medical device sales, biotechnology, PhD/Pharm.D studies, health and wellness coordination and research assistance.
Prior research experience is not required, as the company provides structured training to develop the skills needed for the CRA position.
PACE® CRA Training Program
Medpace provides its PACE® (Professionals Achieving CRA Excellence) Training Program to prepare new CRAs for their responsibilities.
The training program includes:
- Interactive discussions focused on CRA responsibilities.
- Hands-on exercises and practical job-related training.
- Development of skills required to perform CRA duties independently.
- In-house and field-based learning.
- Potential exposure to clinical research departmental rotations.
- Learning about different aspects of drug and medical device development and approval.
This structured training is intended to help candidates transition into the CRA role and develop practical clinical research capabilities.
Key Responsibilities
As a Clinical Research Associate Entry, the selected candidate will be responsible for activities such as:
- Conduct qualification, initiation, monitoring and closeout visits at clinical research sites.
- Ensure site activities are performed according to approved clinical trial protocols.
- Communicate with site personnel, including coordinators, clinical research physicians and other site staff.
- Verify investigator qualifications, training, facilities, laboratories, equipment and staffing resources.
- Review medical records and research source documents against case report form (CRF) data.
- Identify data entry errors and communicate required corrections to site personnel.
- Monitor adherence to Good Documentation Practices.
- Identify and communicate protocol deviations according to applicable SOPs, GCP and regulatory requirements.
- Verify that investigators enroll only eligible study participants.
- Review regulatory documentation maintained by clinical research sites.
- Monitor accountability and inventory of investigational drugs or medical devices, as applicable.
- Review adverse events, serious adverse events, concomitant medications and related illnesses for accurate reporting.
- Assess patient recruitment and retention performance at clinical sites.
- Provide suggestions to sites to support recruitment and retention.
- Prepare monitoring reports and follow-up correspondence.
- Document significant findings, deviations, deficiencies and recommended corrective actions.
Educational Qualification and Eligibility
Required Qualification
Candidates should have:
- Minimum Bachelor’s Degree
Preferred Educational Background
A degree in a health or life science-related field is preferred.
The role may be relevant to graduates from different healthcare and science disciplines, depending on their overall profile.
Experience
The listing indicates 0–1 years of experience, and the job description specifically states that prior research experience is not required.
Previous experience as a Clinical Research Coordinator (CRC) is considered an advantage.
Required Skills
Candidates should have the following skills and capabilities:
- Basic familiarity with clinical research concepts.
- Understanding of healthcare or life science environments.
- Familiarity with Microsoft Office.
- Strong communication skills.
- Good presentation abilities.
- Attention to detail and accurate documentation practices.
- Ability to communicate effectively with clinical research site personnel.
- Ability to work according to protocols, SOPs and applicable regulatory requirements.
- Willingness to travel extensively for clinical site activities.
Travel Requirement
The position requires approximately 60–80% national travel.
Candidates considering this opportunity should be comfortable travelling to clinical research sites as part of their CRA responsibilities.
Work Location and Employment Type
Location: Navi Mumbai, Maharashtra, India
Employment Type: Full-time, Permanent
The vacancy is categorized under Research & Development within the Pharmaceutical & Biotechnology field.
Career Growth and Development
The CRA Entry position provides exposure to clinical trials and multiple aspects of clinical research site management.
According to the job information, Medpace provides defined career paths, onboarding and training programs, ongoing learning opportunities and opportunities for professional development.
The role can also provide exposure to different therapeutic areas and collaboration with physicians, scientists and other clinical research professionals.
Salary / CTC
The vacancy does not disclose a specific salary or CTC. It states that the company offers competitive compensation, but no exact amount is provided.
Candidates can confirm the applicable compensation package during the recruitment process.
Benefits
The listed employee benefits may include:
- Competitive compensation programs.
- Health and wellness benefits.
- Retirement benefits.
- Paid time off (PTO).
- Office-based work culture with occasional work-from-home flexibility for eligible positions after training.
- Company-sponsored social events.
- Training and professional development opportunities.
Benefits may vary depending on the country and applicable company policies.
Selection Process
After an application is submitted, a Medpace team member reviews the candidate’s profile. If the profile matches current hiring requirements, the candidate may be contacted for an interview.
The company notes that applications are reviewed carefully, but only candidates selected for interviews will be contacted.
How to Apply
Interested and eligible candidates can apply online for the Clinical Research Associate Entry position in Navi Mumbai.
Candidates should review the complete job requirements and submit accurate educational and professional details with their application.
Position: Clinical Research Associate Entry
Location: Navi Mumbai, Maharashtra
Experience: 0–1 years
Employment Type: Full-time, Permanent
The vacancy is listed through the Medpace Clinical Research India recruitment page.
Important Details Before Applying
- Company: Medpace Clinical Research India
- Position: Clinical Research Associate Entry
- Location: Navi Mumbai, Maharashtra
- Department: Research & Development
- Experience: 0–1 years
- Qualification: Minimum Bachelor’s Degree
- Preferred Background: Health or Life Science-related field
- Previous Research Experience: Not required
- CRC Experience: An advantage
- Travel: Approximately 60–80% nationally
- Employment Type: Full-time, Permanent
- Key Areas: Clinical trial monitoring, site management, source data verification and regulatory documentation
- Training: PACE® CRA Training Program
Important Note
Job availability, eligibility requirements, compensation, benefits and recruitment procedures may change. Candidates should review the latest employer-provided vacancy information before applying.
The CRA role involves significant national travel, so candidates should consider the travel requirement before submitting their application.
Frequently Asked Questions
1. What position is Medpace hiring for?
Medpace Clinical Research India is hiring for a Clinical Research Associate Entry position.
2. Where is the CRA Entry job located?
The position is based in Navi Mumbai, Maharashtra.
3. Is prior clinical research experience required?
No. The job description states that research experience is not required, as Medpace provides comprehensive initial and ongoing training through its PACE® program.
4. What qualification is required for the CRA Entry position?
A minimum Bachelor’s Degree is required. A background in a health or life science-related field is preferred.
5. Is Clinical Research Coordinator experience required?
No. CRC experience is listed as an advantage, rather than a mandatory requirement.
6. How much travel is involved in this role?
The position requires approximately 60–80% national travel.
7. What does a Clinical Research Associate do?
The role includes clinical site visits, monitoring, source document verification, regulatory document review, investigational product or device accountability, adverse event review, recruitment and retention assessment, and preparation of monitoring reports.
8. What training does Medpace provide?
Medpace provides the PACE® CRA Training Program, which includes interactive learning, hands-on exercises, in-house and field-based training, and potential exposure to other clinical research functions.
