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Clinical Research Coordinator Job in Kolkata at KV Clinical

Clinical Research Coordinator Job in Kolkata at KV Clinical. Pharma candidates can gain trial experience, patient coordination, and regulatory compliance exposure.

Are you looking to grow your career in clinical research and work directly on clinical trials? KV Clinical Research Pvt. Ltd. is hiring Clinical Research Coordinators (CRC) in Kolkata. This role is ideal for candidates with prior clinical research experience who want hands-on exposure to trial coordination, patient management, and regulatory compliance.


Company Overview

KV Clinical Research Pvt. Ltd. is a clinical research organization focused on conducting high-quality clinical trials in compliance with global regulatory standards. The company works closely with investigators, sponsors, and CRO partners to ensure efficient and ethical trial execution. It offers a professional environment for learning and career advancement in clinical research.


Job Overview

Job TitleClinical Research Coordinator (CRC)
CompanyKV Clinical Research Pvt. Ltd.
LocationKolkata, West Bengal, India
Employment TypeFull-Time
DepartmentClinical Research / Site Operations
ExperienceMinimum 1+ Year
QualificationB.Pharm / M.Pharm / PharmD / M.Sc Clinical Research / Diploma
Salary₹2.5 LPA – ₹4.5 LPA (Estimated)
Application ModeEmail Application

Job Location & Employment Type

  • Work Location: Kolkata, West Bengal
  • Job Type: Full-time
  • Work Mode: On-site

Open Positions / Department Details

This role is part of the Clinical Research Site Operations Team, responsible for managing clinical trials at the site level and ensuring compliance with protocols and regulatory requirements.


Key Roles & Responsibilities

As a Clinical Research Coordinator, you will play a crucial role in managing clinical trial activities at the site.

Clinical Trial Coordination

  • Coordinating and managing clinical trial activities
  • Supporting investigators in trial execution
  • Monitoring study progress and timelines
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Patient Management & Recruitment

  • Assisting in patient recruitment and screening
  • Supporting the informed consent process
  • Ensuring patient safety and protocol adherence

Documentation & Data Management

  • Maintaining Trial Master File (TMF)
  • Handling Case Report Forms (CRFs) and data entry
  • Ensuring accurate and complete documentation

Regulatory Compliance

  • Ensuring compliance with:
    • ICH-GCP guidelines
    • Regulatory requirements
  • Reporting deviations and adverse events

Stakeholder Coordination

  • Liaising with:
    • Sponsors
    • CROs
    • Internal teams
  • Ensuring smooth communication and trial execution

Eligibility Criteria

Educational Qualification

Candidates must have:

  • B.Pharm / M.Pharm / PharmD
  • M.Sc in Clinical Research
  • Diploma in Clinical Research

Experience Required

  • Minimum 1+ year of experience in:
    • Clinical trials
    • Clinical Research Coordinator (CRC) role

Skills Required

  • Strong knowledge of:
    • Clinical trial processes
    • ICH-GCP guidelines
    • TMF and CRF handling
  • Good communication and coordination skills
  • Attention to detail and compliance mindset
  • Ability to manage multiple tasks and timelines

Salary & Benefits

  • Estimated Salary: ₹2.5 LPA – ₹4.5 LPA

Benefits:

  • Hands-on experience in clinical trials
  • Opportunity to work with investigators and sponsors
  • Career growth in:
    • Clinical Research
    • CRA roles
    • Regulatory pathways
  • Exposure to GCP-compliant environments

Selection Process

The hiring process may include:

  1. Resume screening
  2. HR interview
  3. Technical interview
  4. Final selection

How to Apply

Interested candidates can apply via email:

Website: www.kvclinicalresearch.com

Application Tips:

  • Highlight CRC experience and clinical trial exposure
  • Mention GCP knowledge and documentation skills

Important Dates

  • No fixed deadline mentioned
  • Early application is recommended

Why Apply for This Pharma Job?

This role is ideal for professionals aiming to build a strong foundation in clinical research. Key benefits include:

  • Work on real-time clinical trials at site level
  • Gain expertise in patient coordination and trial management
  • Exposure to regulatory compliance and documentation
  • Opportunity to grow into CRA and clinical operations roles
  • Work in a structured and learning-focused environment
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Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with KV Clinical Research or any recruiter. We do not charge any fees for job applications. Candidates should verify details before applying.


Final Call-to-Action

If you have clinical research experience and want to advance your career as a CRC, apply now and join KV Clinical Research.


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