Clinical Research Associate (Entry Level)
Location: Navi Mumbai, India
Job ID: 12794
Department: Clinical Research
Job Summary
We are seeking motivated individuals for the role of Clinical Research Associate (Entry Level). Candidates from diverse healthcare and life science backgrounds are encouraged to apply.
Preferred backgrounds include:
Nurses
Dieticians
Pharmacy Technicians
Pharmaceutical or Medical Device Sales Representatives
Biotechnology Engineers
Pharm.D or PhD candidates
Health and Wellness Coordinators
Research Assistants
No prior clinical research experience is required as comprehensive training will be provided through the PACE® – Medpace CRA Training Program.
PACE® – CRA Training Program
The PACE® (Professionals Achieving CRA Excellence) program is designed to develop strong foundational and advanced skills required for Clinical Research Associates.
Key features include:
Structured onboarding with comprehensive initial and ongoing training
Hands-on learning through interactive discussions and practical exercises
Exposure to various aspects of clinical research and drug or device development
Optional departmental rotations for broader understanding of clinical research functions
Development of independent CRA competencies
This program ensures candidates are well-prepared to perform effectively in clinical research environments.
Role Overview and Benefits
This position offers a dynamic career opportunity with:
Exposure to multiple therapeutic areas
Collaboration with clinical and regulatory experts
Defined career progression and promotion pathways
Opportunities for mentoring and leadership development
Competitive compensation and travel-related benefits
Extensive travel across sites within India (approximately 60–80 percent)
Key Responsibilities
Site Management and Monitoring
Conduct qualification, initiation, monitoring, and close-out visits at clinical trial sites
Ensure compliance with approved study protocols and regulatory requirements
Assess investigator qualifications, site facilities, equipment, and staff readiness
Data Verification and Quality Control
Verify source documentation against case report forms (CRFs)
Identify and report data entry errors and protocol deviations
Ensure adherence to Good Documentation Practices, GCP guidelines, SOPs, and regulatory standards
Patient Safety and Study Conduct
Ensure enrollment of eligible study participants only
Review adverse events, serious adverse events, concomitant medications, and related medical history
Ensure accurate and timely clinical data reporting
Regulatory Compliance
Review essential regulatory documentation
Manage investigational product or device accountability and inventory tracking
Communication and Reporting
Communicate effectively with clinical site staff and investigators
Evaluate site recruitment and retention performance and provide recommendations
Prepare monitoring visit reports and follow-up letters
Document findings, deviations, deficiencies, and corrective actions
Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related healthcare field
Clinical Research Coordinator experience will be considered an advantage
Willingness to travel approximately 60–80 percent nationally
Proficiency in Microsoft Office applications
Strong communication and presentation skills
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