Apply for Medpace Hiring Experienced Clinical Research Associate in Navi Mumbai. Experienced professionals can advance clinical research careers.
Introduction
Medpace is actively hiring Experienced Clinical Research Associates (CRA) for its Navi Mumbai office. This opportunity is ideal for clinical research professionals with prior site monitoring experience who are looking to advance their careers in a globally recognized Contract Research Organization (CRO). The position offers extensive exposure to clinical trial management, regulatory compliance, site monitoring, and patient safety activities across multiple therapeutic areas. Candidates with 2–4 years of Clinical Research Associate experience and a passion for advancing healthcare innovation are encouraged to apply. Professionals searching for Clinical Research Jobs, Pharma Jobs 2026, and CRO career opportunities will find this role highly rewarding.
About Company
Medpace is a leading global full-service Contract Research Organization (CRO) dedicated to accelerating the development of safe and effective medical therapies. Headquartered in Cincinnati, Ohio, USA, the company provides comprehensive Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device companies worldwide.
With operations across more than 40 countries and a workforce exceeding 5,000 professionals, Medpace supports clinical trial planning, regulatory affairs, project management, biostatistics, data management, pharmacovigilance, and medical monitoring services. The organization has developed strong expertise in oncology, cardiology, endocrinology, metabolic diseases, central nervous system disorders, anti-viral therapies, and anti-infective treatments.
Recognized globally for scientific excellence and operational quality, Medpace continues to play a significant role in bringing innovative treatments to patients while offering exceptional career growth opportunities for clinical research professionals.
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Job Details / Job Summary
| Particulars | Details |
|---|---|
| Company Name | Medpace |
| Job Role | Experienced Clinical Research Associate |
| Department | Clinical Research Operations |
| Qualification Required | Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Healthcare or Related Field |
| Experience Required | 2–4 Years as Clinical Research Associate |
| Salary Package | ₹8 LPA – ₹15 LPA (Expected) |
| Job Location | Navi Mumbai, Maharashtra |
| Employment Type | Full-Time |
| Industry Type | Clinical Research Organization (CRO) |
| Shift Timing | General Shift |
| Gender Eligibility | Male & Female |
| Application Mode | Online Application |
| Selection Process | Resume Screening, Technical Interview, HR Interview |
| Skills Required | Clinical Monitoring, GCP, Regulatory Compliance, Site Management |
| Official Notification Status | Active |
| Application Last Date | Apply As Soon As Possible |
Eligibility Criteria
Applicants should fulfill the following requirements:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Healthcare, or related discipline.
- Minimum 2 to 4 years of experience as a Clinical Research Associate.
- Prior clinical site monitoring experience is essential.
- Strong understanding of Good Clinical Practice (GCP) guidelines.
- Willingness to travel approximately 60–80% nationally.
- Proficiency in Microsoft Office applications.
- Strong communication and presentation skills.
- Ability to manage multiple clinical sites and priorities effectively.
Required Skills
Successful candidates should possess expertise in:
- Clinical Trial Monitoring
- Site Qualification and Initiation Visits
- Site Closeout Activities
- Good Clinical Practice (GCP)
- Regulatory Documentation Review
- Investigational Product Accountability
- Adverse Event Review and Reporting
- Source Data Verification (SDV)
- Clinical Trial Compliance
- Patient Recruitment Assessment
- Risk Identification and Mitigation
- Clinical Operations Management
- Communication and Stakeholder Management
- Monitoring Report Preparation
These competencies are highly valuable for professionals pursuing Clinical Research Jobs, Regulatory Affairs Jobs, and advanced CRO career opportunities.
Roles and Responsibilities
As an Experienced Clinical Research Associate, your responsibilities will include:
- Conducting qualification, initiation, monitoring, and closeout visits at research sites.
- Ensuring protocol compliance throughout study execution.
- Collaborating with investigators, site coordinators, and healthcare professionals.
- Verifying investigator qualifications, facilities, resources, and staff readiness.
- Performing source data verification and reviewing case report forms.
- Identifying and documenting protocol deviations according to SOPs and GCP requirements.
- Ensuring enrollment of eligible study participants only.
- Reviewing and maintaining essential regulatory documents.
- Managing investigational product and medical device accountability.
- Reviewing adverse events, serious adverse events, and concomitant medications.
- Assessing patient recruitment and retention strategies at study sites.
- Preparing monitoring reports and site follow-up documentation.
- Recommending corrective and preventive actions to maintain compliance standards.
PACE® Clinical Research Associate Training Program
Medpace provides ongoing development through its renowned PACE® Training Program.
The program offers:
- Advanced CRA skill development.
- Practical monitoring exercises.
- Interactive clinical research workshops.
- Cross-functional department exposure.
- Continuous professional development opportunities.
- Leadership and career advancement preparation.
Even experienced CRAs benefit from Medpace’s structured learning environment and professional development initiatives.
Home-Based Work Opportunity
One of the key advantages of this role is the availability of a home-based work option for Clinical Research Associates with more than one year of monitoring experience.
This flexibility allows professionals to maintain work-life balance while continuing to support clinical trials across multiple locations.
Salary Details
The expected salary package for the Experienced Clinical Research Associate position ranges between ₹8 LPA and ₹15 LPA, depending on:
- Years of CRA experience
- Monitoring expertise
- Therapeutic area exposure
- Clinical trial management skills
- Interview performance
Additional benefits may include:
- Travel allowances and bonuses
- Health and wellness programs
- Performance-based incentives
- Career progression opportunities
- Flexible work arrangements
- Employee appreciation programs
Selection Process
The recruitment process generally includes the following stages:
Step 1: Online Application
Candidates submit their applications through the official Medpace careers portal.
Step 2: Resume Screening
Recruiters evaluate qualifications, monitoring experience, and clinical research background.
Step 3: Technical Assessment
Candidates may be assessed on GCP, monitoring practices, and clinical trial knowledge.
Step 4: Hiring Manager Interview
Shortlisted applicants participate in discussions with clinical operations leaders.
Step 5: HR Interview
Final discussions regarding compensation, availability, and organizational fit.
Step 6: Offer and Onboarding
Successful candidates receive an employment offer and onboarding instructions.
Why Join Medpace?
Medpace offers numerous career advantages for experienced CRAs:
- Global clinical research exposure.
- Structured CRA career advancement framework.
- Opportunities for mentoring and leadership growth.
- Competitive salary and travel bonus programs.
- Flexible work environment.
- Exposure to multiple therapeutic areas.
- Collaboration with regulatory and scientific experts.
- Strong employee development culture.
How to Apply
Interested and eligible candidates can apply through the official Medpace recruitment portal.
Before applying:
- Update your latest resume with detailed CRA experience.
- Highlight monitoring visits, therapeutic areas, and regulatory expertise.
- Include certifications and relevant clinical research training.
- Verify all contact details before submission.
- Apply online as early as possible.
Professionals seeking Clinical Research Jobs, Pharma Jobs 2026, Regulatory Affairs Jobs, and advanced CRO opportunities are encouraged to apply.
Frequently Asked Questions (FAQs)
1. What qualification is required for the Medpace Experienced CRA position?
Candidates should possess a bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Healthcare, or a related field.
2. Can freshers apply for this Clinical Research Associate vacancy?
No. This position specifically requires 2–4 years of Clinical Research Associate experience.
3. What is the expected salary for this role?
The expected salary package ranges from ₹8 LPA to ₹15 LPA based on experience and qualifications.
4. How can I apply for the Medpace Experienced CRA job?
Eligible candidates can submit their applications through the official Medpace careers portal.
