Medpace Hiring Clinical Research Associate (CRA) – Navi Mumbai

Pharma Hiring Hub; Mumbai; On-site; INR 350,000 - 550,000; Full time

Benefits offered by this job

Paid CRA training

Global exposure

Travel across India

Job summary

Medpace Clinical Research India Pvt. Ltd. invites fresh graduates to join as Clinical Research Associate (CRA) – Entry at Navi Mumbai. No prior monitoring experience required; successful candidates will undergo Medpace’s PACE® CRA Training Program before taking on independent monitoring activities.

This role offers international exposure in clinical research, comprehensive training, and a clear career path within a globally respected CRO, with travel across India to study sites and sponsors.

Qualifications

• Fresh graduates encouraged to apply.
• 0–2 years of experience; freshers eligible.
• Qualifications include B.Pharm, M.Pharm, Pharm.D, Nursing, Biotechnology & Life Sciences.

Responsibilities

• Monitor clinical studies to ensure compliance with ICH-GCP and protocols.
• Visit and monitor sites; verify regulatory documentation and AE/SAE reporting.
• Prepare monitoring reports and communicate findings to investigators.

Skills

CRA Monitoring

Regulatory Compliance

GCP Knowledge

Communication Skills

Education

B.Pharm

M.Pharm

Pharm.D

Nursing

Biotechnology & Life Sciences

Job description

Clinical Research Associates (CRAs) are among the most sought-after professionals in the pharmaceutical and clinical research industry. They play a crucial role in ensuring that clinical trials are conducted according to international regulatory standards while protecting participant safety and maintaining the integrity of clinical data. As the clinical research industry continues to expand across India, the demand for skilled CRAs is increasing rapidly, making it an excellent career choice for pharmacy and life sciences graduates.

Medpace Clinical Research India has announced an exciting opportunity for fresh graduates by opening applications for the position of Clinical Research Associate (CRA) – Entry at its Navi Mumbai office. One of the biggest advantages of this opportunity is that prior monitoring experience is not mandatory. Selected candidates receive comprehensive training through Medpace’s globally recognized PACE® (Professionals Achieving CRA Excellence) Training Program before taking responsibility for independent monitoring activities.

If you are passionate about clinical research, patient safety, and drug development while looking for a career with international exposure, this opportunity could be the ideal starting point.

Job Overview

Particulars

Details

Company Medpace Clinical Research India Pvt. Ltd.

Position Clinical Research Associate (CRA) – Entry

Location Navi Mumbai (Ghansoli)

Employment Type Full-Time

Experience 0–2 Years (Freshers Eligible)

Qualification B.Pharm, M.Pharm, Pharm.D, Nursing, Biotechnology & Life Sciences

Training PACE® CRA Training Program

Travel Requirement 60–80% National Travel

About Medpace

Medpace is a globally recognized Contract Research Organization (CRO) providing clinical development services to pharmaceutical, biotechnology, and medical device companies. The organization manages studies across multiple therapeutic areas and supports sponsors from early clinical development through regulatory approval.

The company is known for investing heavily in employee development and is widely respected for its structured CRA training program, making it one of the preferred employers for candidates starting careers in clinical research.

What Does a Clinical Research Associate Do?

A Clinical Research Associate acts as the bridge between the sponsor, Contract Research Organization, and clinical trial sites. Their primary responsibility is to monitor clinical studies and ensure that every trial follows Good Clinical Practice (GCP), study protocols, and regulatory requirements.

CRAs regularly visit hospitals and research sites to review patient records, verify study documentation, assess investigational product accountability, and ensure accurate reporting of clinical data. Their work directly contributes to patient safety and the successful completion of clinical trials.

Key Responsibilities

• Conduct Site Qualification, Site Initiation, Monitoring, and Close-Out Visits.
• Identify protocol deviations and documentation discrepancies.
• Maintain communication with investigators and study coordinators.
• Review Investigator Site Files and regulatory documents.
• Audit investigational product accountability records.
• Verify reporting of Adverse Events (AE) and Serious Adverse Events (SAE).
• Prepare monitoring reports and follow-up letters.
• Ensure compliance with ICH‑GCP and study protocols.
• Support successful completion of global clinical trials.

One of the biggest advantages of joining Medpace is its internationally recognized PACE® CRA Training Program. Instead of expecting fresh graduates to possess monitoring experience, the company provides structured classroom learning and practical exposure before assigning independent monitoring responsibilities.

• Interactive classroom training.
• Clinical trial case studies.
• Mock site monitoring exercises.
• Site visit simulations.
• Rotations across Clinical Operations, Data Management, and Drug Safety.
• Mentorship from experienced Clinical Research Associates.

Eligibility Criteria

• B.Pharm
• M.Pharm
• Pharm.D
• Nursing
• Physiotherapy
• Biotechnology
• Microbiology
• Biomedical Sciences
• Other Health or Life Science Degrees

Fresh graduates are encouraged to apply. Previous experience as a Clinical Research Coordinator or Research Assistant can be an added advantage.

Why Join Medpace?

• Paid structured CRA training.
• Global clinical research exposure.
• Excellent career growth opportunities.
• International monitoring experience.
• Exposure to multiple therapeutic areas.
• Travel opportunities across India.
• Learning-focused work environment.

A Clinical Research Associate role provides excellent long-term career opportunities. With experience, professionals can advance to Senior CRA, Lead CRA, Clinical Trial Manager, Project Manager, Clinical Operations Manager, and eventually leadership positions within global pharmaceutical companies and CROs.

Resume Tips

• Mention GCP certifications if available.
• Highlight Clinical Research Coordinator experience.
• Include patient interaction or hospital exposure.
• Showcase communication and presentation skills.
• Mention clinical research internships.
• Keep your resume ATS‑friendly and well‑structured.