Clinical Research Associate (CRA Entry)

Medpace Clinical Research India
๐Ÿ‘œ 0 - 1 years
๐Ÿ“ Navi Mumbai, Maharashtra
Posted on June 02, 2026

Brief Summary:

Medpace is seeking motivated professionals to support clinical trial monitoring activities across multiple therapeutic areas. Selected candidates will be responsible for ensuring regulatory compliance, site management, patient safety oversight, data quality, and successful execution of clinical studies.

This opportunity provides exposure to global clinical development programs and offers a strong foundation for career growth within the clinical research industry.

Job Description:

๐Ÿš€ WEโ€™RE HIRING | Clinical Research Associates (CRA Entry & Experienced CRA) | Medpace Clinical Research India | Navi Mumbai ๐Ÿš€

Looking for Clinical Research Associate jobs in India? Medpace Clinical Research India is hiring both Entry-Level Clinical Research Associates and Experienced CRAs for its Navi Mumbai office.

This is an excellent opportunity for B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, Nursing, Clinical Research professionals, Research Assistants, and candidates looking to build a long-term career in clinical trials monitoring and clinical research operations.

One of the biggest highlights of this opportunity is Medpaceโ€™s globally recognized PACEยฎ Clinical Research Associate Training Program, designed to help freshers transition successfully into the clinical research industry.

๐Ÿข Company: Medpace Clinical Research India
๐ŸŒ Industry: Clinical Research / CRO
๐Ÿ‘‰ Role: Clinical Research Associate (CRA Entry) & Experienced Clinical Research Associate
๐Ÿ’ผ Experience: 0โ€“1 Year (Entry CRA) | 2โ€“4 Years (Experienced CRA)
๐Ÿ“ Location: Navi Mumbai, Maharashtra
๐Ÿข Work Mode: On-site
๐Ÿ•’ Employment Type: Full-Time, Permanent
โœˆ Travel Requirement: 60โ€“80% National Travel

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿ”ง Key Responsibilities
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿ“Œ Site Management & Monitoring
โœ” Conduct Site Qualification Visits (SQV)
โœ” Perform Site Initiation Visits (SIV)
โœ” Conduct Routine Monitoring Visits (MV)
โœ” Execute Close-Out Visits (COV)

๐Ÿ“Œ Clinical Trial Compliance
โœ” Verify investigator qualifications and training
โœ” Review regulatory documentation
โœ” Ensure protocol compliance
โœ” Monitor adherence to ICH-GCP guidelines

๐Ÿ“Œ Source Data Verification
โœ” Compare source documents with Case Report Forms (CRFs)
โœ” Identify and resolve data discrepancies
โœ” Ensure Good Documentation Practices (GDP)

๐Ÿ“Œ Safety Monitoring
โœ” Review Adverse Events (AE)
โœ” Verify Serious Adverse Events (SAE)
โœ” Assess concomitant medications and medical history

๐Ÿ“Œ Investigational Product Accountability
โœ” Verify drug/device inventory
โœ” Review storage conditions
โœ” Ensure accountability compliance

๐Ÿ“Œ Site Performance Management
โœ” Assess patient recruitment activities
โœ” Evaluate patient retention rates
โœ” Recommend process improvements

๐Ÿ“Œ Reporting Activities
โœ” Prepare monitoring visit reports
โœ” Generate follow-up letters
โœ” Document findings and corrective actions

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐ŸŽ“ Eligibility Criteria
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿ“Œ CRA Entry Position
โœ” Bachelorโ€™s Degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Clinical Research, or related healthcare disciplines
โœ” Strong communication skills
โœ” Basic Microsoft Office knowledge
โœ” Willingness to travel extensively across India

๐Ÿ“Œ Preferred Educational Backgrounds
โœ” B.Pharm
โœ” M.Pharm
โœ” Pharm.D
โœ” B.Sc Life Sciences
โœ” M.Sc
โœ” Biotechnology
โœ” Clinical Research
โœ” Nursing
โœ” Research Assistants
โœ” Pharmacy Technicians

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿ›  Required Skills
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
โœ… Clinical Trial Monitoring
โœ… Site Management
โœ… ICH-GCP Compliance
โœ… Clinical Documentation Review
โœ… Source Data Verification
โœ… Regulatory Documentation
โœ… Clinical Operations
โœ… Safety Monitoring
โœ… Investigational Product Accountability
โœ… Monitoring Visit Reporting
โœ… Communication & Stakeholder Management
โœ… Problem-Solving Skills

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐ŸŽ“ Medpace PACEยฎ CRA Training Program
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
One of the major attractions of this opportunity is Medpaceโ€™s industry-recognized PACEยฎ Clinical Research Associate Training Program.

The program includes:

โœ” Comprehensive CRA onboarding
โœ” Interactive learning sessions
โœ” Practical clinical monitoring exercises
โœ” Hands-on training
โœ” Exposure to multiple clinical research functions
โœ” Career development support

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿ’ฐ Salary & Benefits
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿ“Œ Expected Annual Compensation

๐Ÿ’ต CRA Entry: โ‚น5.5 LPA โ€“ โ‚น8 LPA
๐Ÿ’ต Experienced CRA: โ‚น8 LPA โ€“ โ‚น14 LPA

โœจ Additional Benefits
โœ” Travel bonus opportunities
โœ” Flexible work environment
โœ” Structured career progression
โœ” Employee wellness programs
โœ” Paid time off benefits
โœ” Professional development opportunities
โœ” Employee recognition programs

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐ŸŒŸ Why Join Medpace?
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
โœจ Opportunity to work with a leading global CRO
โœจ Exposure to international clinical trials and drug development programs
โœจ Industry-recognized CRA training and career development
โœจ Strong growth opportunities within clinical operations
โœจ Exposure to multiple therapeutic areas
โœจ Collaborative and learning-focused work environment
โœจ Global career opportunities across clinical research functions

โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
๐Ÿš€ Why Choose a Career as a Clinical Research Associate?
โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”โ”
โœ” High demand across CROs and pharmaceutical companies
โœ” International career opportunities
โœ” Attractive compensation packages
โœ” Exposure to clinical trials and drug development
โœ” Strong career growth pathways into Clinical Trial Management, Clinical Operations, and Project Management
โœ” Opportunity to contribute to the development of innovative therapies and medicines


๐Ÿ” Referrals are highly appreciated!

โšก If you are passionate about clinical research, clinical trials, and patient-focused drug development, Medpace offers an excellent platform to build a rewarding and long-term career in the global clinical research industry.

Required Skills:

โœ… Clinical Trial Monitoring โœ… Site Management โœ… ICH-GCP Compliance โœ… Clinical Documentation Review โœ… Source Data Verification โœ… Regulatory Documentation โœ… Clinical Operations โœ… Safety Monitoring โœ… Investigational Product Accountability โœ… Monitoring Visit Reporting โœ… Communication & Stakeholder Management โœ… Problem-Solving Skills

About Medpace Clinical Research India

Medpace is a leading global Contract Research Organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device companies worldwide.

Headquartered in Cincinnati, Ohio, Medpace operates in more than 40 countries and employs over 5,000 professionals globally.

๐Ÿ”ฌ Therapeutic Areas Include:
โœ” Oncology
โœ” Cardiology
โœ” Endocrinology
โœ” Metabolic Diseases
โœ” Central Nervous System Disorders
โœ” Anti-Infective Research
โœ” Anti-Viral Research
โœ” Verified