Clinical Research Associate (CRA Entry)
Brief Summary:
This opportunity provides exposure to global clinical development programs and offers a strong foundation for career growth within the clinical research industry.
Job Description:
๐ WEโRE HIRING | Clinical Research Associates (CRA Entry & Experienced CRA) | Medpace Clinical Research India | Navi Mumbai ๐
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 Medpaceโs globally recognized PACEยฎ Clinical Research Associate Training Program, designed to help freshers transition successfully into the clinical research industry.
๐ข Company: Medpace Clinical Research India
๐ Industry: Clinical Research / CRO
๐ Role: Clinical Research Associate (CRA Entry) & Experienced Clinical Research Associate
๐ผ Experience: 0โ1 Year (Entry CRA) | 2โ4 Years (Experienced CRA)
๐ Location: Navi Mumbai, Maharashtra
๐ข Work Mode: On-site
๐ Employment Type: Full-Time, Permanent
โ Travel Requirement: 60โ80% National Travel
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๐ง Key Responsibilities
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๐ Site Management & Monitoring
โ Conduct Site Qualification Visits (SQV)
โ Perform Site Initiation Visits (SIV)
โ Conduct Routine Monitoring Visits (MV)
โ Execute Close-Out Visits (COV)
๐ Clinical Trial Compliance
โ Verify investigator qualifications and training
โ Review regulatory documentation
โ Ensure protocol compliance
โ Monitor adherence to ICH-GCP guidelines
๐ Source Data Verification
โ Compare source documents with Case Report Forms (CRFs)
โ Identify and resolve data discrepancies
โ Ensure Good Documentation Practices (GDP)
๐ Safety Monitoring
โ Review Adverse Events (AE)
โ Verify Serious Adverse Events (SAE)
โ Assess concomitant medications and medical history
๐ Investigational Product Accountability
โ Verify drug/device inventory
โ Review storage conditions
โ Ensure accountability compliance
๐ Site Performance Management
โ Assess patient recruitment activities
โ Evaluate patient retention rates
โ Recommend process improvements
๐ Reporting Activities
โ Prepare monitoring visit reports
โ Generate follow-up letters
โ Document findings and corrective actions
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๐ Eligibility Criteria
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๐ CRA Entry Position
โ Bachelorโs Degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Clinical Research, or related healthcare disciplines
โ Strong communication skills
โ Basic Microsoft Office knowledge
โ Willingness to travel extensively across India
๐ Preferred Educational Backgrounds
โ B.Pharm
โ M.Pharm
โ Pharm.D
โ B.Sc Life Sciences
โ M.Sc
โ Biotechnology
โ Clinical Research
โ Nursing
โ Research Assistants
โ Pharmacy Technicians
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๐ Required Skills
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Clinical Trial Monitoring
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Site Management
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ICH-GCP Compliance
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Clinical Documentation Review
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Source Data Verification
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Regulatory Documentation
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Clinical Operations
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Safety Monitoring
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Investigational Product Accountability
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Monitoring Visit Reporting
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Communication & Stakeholder Management
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Problem-Solving Skills
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๐ Medpace PACEยฎ CRA Training Program
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One of the major attractions of this opportunity is Medpaceโs industry-recognized PACEยฎ Clinical Research Associate Training Program.
The program includes:
โ Comprehensive CRA onboarding
โ Interactive learning sessions
โ Practical clinical monitoring exercises
โ Hands-on training
โ Exposure to multiple clinical research functions
โ Career development support
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๐ฐ Salary & Benefits
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๐ Expected Annual Compensation
๐ต CRA Entry: โน5.5 LPA โ โน8 LPA
๐ต Experienced CRA: โน8 LPA โ โน14 LPA
โจ Additional Benefits
โ Travel bonus opportunities
โ Flexible work environment
โ Structured career progression
โ Employee wellness programs
โ Paid time off benefits
โ Professional development opportunities
โ Employee recognition programs
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๐ Why Join Medpace?
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โจ Opportunity to work with a leading global CRO
โจ Exposure to international clinical trials and drug development programs
โจ Industry-recognized CRA training and career development
โจ Strong growth opportunities within clinical operations
โจ Exposure to multiple therapeutic areas
โจ Collaborative and learning-focused work environment
โจ Global career opportunities across clinical research functions
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๐ Why Choose a Career as a Clinical Research Associate?
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โ High demand across CROs and pharmaceutical companies
โ International career opportunities
โ Attractive compensation packages
โ Exposure to clinical trials and drug development
โ Strong career growth pathways into Clinical Trial Management, Clinical Operations, and Project Management
โ Opportunity to contribute to the development of innovative therapies and medicines
๐ Referrals are highly appreciated!
โก 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:
About Medpace Clinical Research India
Headquartered in Cincinnati, Ohio, Medpace operates in more than 40 countries and employs over 5,000 professionals globally.
๐ฌ Therapeutic Areas Include:
โ Oncology
โ Cardiology
โ Endocrinology
โ Metabolic Diseases
โ Central Nervous System Disorders
โ Anti-Infective Research
โ Anti-Viral Research