Clinical Research Associate Job at Meril in Vapi, Gujarat, India

Meril is hiring a Meril Clinical Research Associate / Clinical Research Coordinator in Vapi, Gujarat, India. The role is full-time, on-site, and requires 2-4 years of experience.

Job Details

  • Company: Meril
  • Job Title: Clinical Research Associate
  • Location: Vapi, Gujarat, India
  • Work Mode: On-site
  • Employment Type: Full-time
  • Experience Required: 2-4 Years

Job Description

We are looking for a proactive and result-oriented Clinical Research Associate / Clinical Research Coordinator to develop and maintain collaborations with hospitals, medical colleges, diagnostic centres, clinicians, and research institutions for healthcare research and AI-based medical technology projects.

Key Responsibilities

  • Identify and establish collaborations with potential hospitals, healthcare institutions, clinicians, and research partners.
  • Conduct field visits, introductory meetings, and follow-ups with medical professionals and institutional stakeholders.
  • Assess site feasibility, institutional capabilities, and potential collaboration opportunities.
  • Coordinate institutional documentation, agreements, ethics committee submissions, and approval follow-ups.
  • Facilitate site onboarding and coordinate project initiation activities after the necessary approvals.
  • Coordinate with clinical sites for study-related requirements, data collection, documentation, and project deliverables.
  • Maintain site collaboration trackers, visit reports, meeting minutes, and progress updates.
  • Liaise with internal teams to resolve operational issues and ensure timely execution of assigned activities.
  • Build and maintain professional relationships with existing and prospective collaborators.
  • Achieve assigned targets for site development, collaboration progress, and project execution.

Required Skills

  • Strong communication, interpersonal, and relationship-management skills.
  • Willingness to travel and independently manage assigned geographical areas.
  • Good documentation, reporting, and follow-up skills.
  • Proficiency in MS Office and email communication.
  • Basic knowledge of clinical research and institutional ethics processes.
  • Ability to manage multiple stakeholders and work toward defined targets.

Additional Information

Preferred Candidate: Profile Candidates with a Life Sciences background who are confident in interacting with healthcare professionals, conducting institutional visits, and developing long-term clinical collaborations.

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Applications can be submitted through the original notification.