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About Company

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:

Position Name :

Clinical Research Associate Entry

Organization :

Medpace

Qualification:

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Experience:

0 YEARS / Freshers - 1 Year

Salary:

25,000 - 35,000 /month

Location:

mumbai

This role takes you on a journey through travel and excitement, allowing you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

  • Dynamic working environment with varying responsibilities day-to-day
  • Expansive experience in multiple therapeutic areas
  • Work within a team of therapeutic and regulatory experts
  • Defined CRA promotion and growth ladder with potential for mentoring and management advancements
  • Competitive pay and opportunity for a significant travel bonus

Responsibilities:
As a CRA Entry, you will specifically be responsible for the following:

  • Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
  • Verifying adequate investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are adhered to, and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
  • Verification that the investigator is enrolling only eligible subjects
  • Regulatory document review
  • Medical device and/or investigational product/drug accountability and inventory
  • Verification and review of adverse events, serious adverse events, concomitant medications, and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
  • Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications:

  • Minimum of a bachelor’s degree; Health or life science-related field preferred
  • Candidates with Clinical Research Coordinator experience are an advantage
  • Willing to travel approximately 60-80% nationally
  • Familiarity with Microsoft® Office
  • Strong communication and presentation skills are a plus

Application Link