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Clinical Research Coordinator (Crc)

Dhanvantari Clinical Research Solutions
1-4 years
preferred by company
Bangalore, Mysore, India
1 May 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment

Job Description – Clinical Research Coordinator (CRC)

Job Title: Clinical Research Coordinator
Location: Mysore / Bangalore
Job Type: Full-Time
Joining: Immediate Joiners Preferred

About the Role

We are looking for a detail-oriented and proactive Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies while ensuring compliance with regulatory guidelines, study protocols, and ethical standards.

Key Responsibilities

  • Coordinate and manage day-to-day clinical trial activities.
  • Screen, recruit, and enroll eligible study participants.
  • Ensure informed consent is obtained and properly documented.
  • Maintain accurate clinical trial documentation, source documents, and case report forms (CRFs).
  • Coordinate with investigators, sponsors, CROs, and site staff.
  • Schedule patient visits and follow-up appointments as per protocol.
  • Monitor study progress and ensure protocol adherence.
  • Report adverse events and safety-related information promptly.
  • Assist during monitoring visits, audits, and inspections.
  • Ensure compliance with ICH-GCP, SOPs, regulatory, and ethical guidelines.
  • Manage study-related inventory, investigational products, and essential documents.

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Clinical Research, or related field.
  • 1–4 years of experience in clinical research coordination.
  • Strong knowledge of GCP, clinical trial documentation, and regulatory compliance.
  • Good communication and interpersonal skills.
  • Ability to handle multiple studies and meet deadlines.

Preferred Skills

  • Experience in patient coordination and site management.
  • Familiarity with EDC systems and medical terminology.
  • Strong documentation and organizational skills.