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Clinical Research Associate Entry

Medpace Clinical Research India

Navi Mumbai, Maharashtra, India · Full Time

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Experience
Any
Salary
—
Openings
1
Posted
2 weeks ago
Work mode
In office
Education
Any graduate
Eligibility
Any graduate is eligible to apply for this position, with a preference for candidates holding qualifications in health or life science disciplines.
Resume
Required to apply

Where you'll work

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Job description

About Medpace

Medpace is a comprehensive clinical contract research organization focused on expediting the development of medical therapeutics. Operating globally with expertise in numerous therapeutic fields such as oncology, cardiology, endocrinology, and infectious diseases, Medpace prides itself on delivering efficient, high-quality clinical trial services. The company supports every phase of clinical trials through regulatory and therapeutic experts to ensure streamlined paths to approval.

Position Overview

The Clinical Research Associate (CRA) Entry position welcomes candidates from diverse healthcare and science backgrounds including nursing, dietetics, pharmacy, biotechnology, health coordination, and research assistance. No prior research experience is necessary as comprehensive training is provided through the PACE® training program which equips candidates with necessary CRA skills and facilitates hands-on practical learning and departmental rotations.

Responsibilities

  • Perform qualification, initiation, monitoring, and closeout visits in accordance with approved clinical protocols.
  • Liaise closely with medical site staff such as coordinators and clinical research physicians to ensure effective communication.
  • Confirm investigator credentials, training, and availability of appropriate facilities and staff.
  • Audit medical records and source documentation against case report forms to ensure accuracy, correct errors, and uphold good documentation practices.
  • Ensure enrollment of eligible subjects only and monitor regulatory compliance.
  • Review regulatory documents, and oversee accountability for investigational drugs or devices.
  • Verify adverse events and concomitant medications are properly documented as per protocols.
  • Evaluate site’s subject recruitment and retention strategies and recommend enhancements.
  • Draft and submit monitoring reports and follow-up communications summarizing observations, deviations, and corrective recommendations.

Qualifications

  • Bachelor's degree required; degrees in health or life sciences preferred.
  • Experience as a Clinical Research Coordinator is advantageous.
  • Willingness to travel extensively within the country (approximately 60-80%).
  • Proficiency in Microsoft Office applications.
  • Strong communication and presentation capabilities are desirable.

Professional Development and Culture

The role offers a dynamic, team-oriented environment where you work with physicians and scientists to bring innovative therapies to patients worldwide. Medpace emphasizes continuous learning, leadership accessibility, and a collaborative culture. Its structured career progression and industry-leading training programs promote rapid professional growth. Employees benefit from competitive compensation, comprehensive health and wellness benefits, flexible work arrangements post-training, and social events.

Additional Information

This role requires national travel of up to 80%, entails working in an office environment with occasional work-from-home flexibility after initial training, and offers competitive remuneration along with potential travel bonuses. Candidates who join Medpace embark on a rewarding career path focused on clinical research excellence and improving patient outcomes globally.

Minimum education

Bachelor's Degree

Tools & software

Microsoft Office required

How they work

Communication Teamwork & Collaboration Attention to Detail Time Management Presentation Skills

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