Medpace Hiring Clinical Research Associates (CRA Entry & Experienced CRA) | 0–4 Years
Medpace Clinical Research India is hiring both Entry-Level Clinical Research Associates (CRA) and Experienced Clinical Research Associates for its Navi Mumbai office. This is an excellent opportunity for Life Sciences, Pharmacy, Biotechnology, Nursing, and Clinical Research professionals looking to build a career in clinical trial monitoring.
A major highlight of this opportunity is Medpace's globally recognized PACE® Clinical Research Associate Training Program, designed to help aspiring CRAs develop industry-ready monitoring skills.
📋 Job Overview
| Details | Information |
|---|---|
| Company | Medpace Clinical Research India |
| Position | Clinical Research Associate (Entry) & Experienced CRA |
| Location | Navi Mumbai, Maharashtra |
| Employment Type | Full-Time, Permanent |
| Experience | 0–1 Year (Entry CRA) | 2–4 Years (Experienced CRA) |
| Industry | Clinical Research / CRO |
| Travel Requirement | 60–80% National Travel |
💰 Experienced CRA: ₹8 LPA – ₹14 LPA
🏢 About Medpace
Medpace is a leading global Contract Research Organization (CRO) providing Phase I-IV clinical development services to pharmaceutical, biotechnology, and medical device companies worldwide. The organization operates in more than 40 countries and supports global clinical development programs across multiple therapeutic areas.
Key Therapeutic Areas:
- Oncology
- Cardiology
- Endocrinology
- Metabolic Diseases
- Central Nervous System Disorders
- Anti-Infective Research
- Anti-Viral Research
📌 Key Responsibilities
Site Management & Monitoring
- Conduct Site Qualification Visits (SQV).
- Perform Site Initiation Visits (SIV).
- Conduct Monitoring Visits (MV).
- Execute Close-Out Visits (COV).
Clinical Trial Compliance
- Verify investigator qualifications and training.
- Review regulatory documentation.
- Ensure protocol compliance.
- Monitor adherence to ICH-GCP guidelines.
Source Data Verification
- Compare source documents with Case Report Forms (CRFs).
- Identify and resolve data discrepancies.
- Ensure Good Documentation Practices (GDP).
Safety Monitoring
- Review Adverse Events (AE).
- Verify Serious Adverse Events (SAE).
- Assess concomitant medications and medical history.
Investigational Product Accountability
- Verify drug/device inventory.
- Review storage conditions.
- Ensure accountability compliance.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Clinical Research
- Nursing
- Research Assistants
- Pharmacy Technicians
CRA Entry Position:
- 0–1 Year Experience.
- Strong communication skills.
- Basic Microsoft Office knowledge.
- Willingness to travel across India.
Experienced CRA Position:
- 2–4 Years Clinical Monitoring Experience.
- Knowledge of ICH-GCP Guidelines.
- Clinical Trial Monitoring Experience.
🎓 Medpace PACE® CRA Training Program
One of the biggest advantages of joining Medpace is the globally recognized PACE® Clinical Research Associate Training Program.
The program is specifically designed to help aspiring Clinical Research Associates develop practical monitoring skills and build successful careers in clinical research.
- Comprehensive CRA onboarding program.
- Interactive learning sessions.
- Practical clinical monitoring exercises.
- Hands-on training.
- Exposure to multiple clinical research functions.
- Career development support.
- Structured mentorship opportunities.
🎁 Salary & Benefits
💰 Experienced CRA: ₹8 LPA – ₹14 LPA
- Travel bonus opportunities.
- Flexible work environment.
- Structured career progression.
- Employee wellness programs.
- Paid time off benefits.
- Professional development opportunities.
- Employee recognition programs.
- Global clinical trial exposure.
🚀 Why Choose a Career as a Clinical Research Associate?
- High demand across CROs and pharmaceutical companies.
- International career opportunities.
- Exposure to clinical trials and drug development.
- Attractive compensation packages.
- Strong career progression into Lead CRA, CTM, and Project Management roles.
- Opportunity to work directly with investigators and clinical trial sites.
👨⚕️ Who Should Apply?
- Life Sciences Graduates.
- B.Pharm, M.Pharm & Pharm.D Professionals.
- Clinical Research Coordinators (CRC).
- Nurses.
- Research Assistants.
- Clinical Trial Assistants (CTA).
- Biotechnology Graduates.
- Professionals seeking CRA career growth.
📄 Resume & Interview Preparation Tips
- Highlight clinical research, internships, CRC, CTA, or site experience.
- Mention ICH-GCP knowledge and clinical trial exposure.
- Include monitoring, documentation, and regulatory activities if applicable.
- Showcase communication, site management, and organizational skills.
- Use an ATS-friendly resume format.
📝 How to Apply
- Select the position you want to apply for.
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Complete the 15-second countdown timer to unlock the application button.
- Apply only if your qualifications match the role requirements.
🚀 Job Application Link
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
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