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CLINICA Research Solutions Hiring For Clinical Trial Assistant

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CLINICA Research Solutions LLP

Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, or a related healthcare

Navi Mumbai, Maharashtra

1 Year

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CLINICA Research Solutions LLP is hiring a Clinical Trial Assistant (CTA) for its Navi Mumbai office. This is an excellent opportunity for professionals with at least one year of clinical research experience to work closely with clinical trial documentation, site coordination, and clinical operations in a growing research organization.

If you have a solid understanding of GCP guidelines, clinical trial documentation, and site management, this Clinical Trial Assistant job in Navi Mumbai could be your next career move.


Job Overview

Job DetailsInformation
CompanyCLINICA Research Solutions LLP
PositionClinical Trial Assistant (CTA)
Job LocationNavi Mumbai, Maharashtra
Employment TypeFull-Time
Work ModeWork From Office
ExperienceMinimum 1 Year as Clinical Research Coordinator (CRC)
QualificationExperience in Clinical Research Coordination
Salary₹2.8 – ₹4 LPA
FreshersNot Eligible

Key Responsibilities

As a Clinical Trial Assistant (CTA), you will be responsible for:

  • Supporting day-to-day clinical trial operations.
  • Maintaining accurate clinical trial documentation.
  • Coordinating with clinical research sites and investigators.
  • Assisting in Trial Master File (TMF) documentation and record management.
  • Ensuring compliance with Good Clinical Practice (GCP) guidelines.
  • Tracking study-related documents and timelines.
  • Supporting communication between sponsors, CRO teams, and study sites.
  • Assisting in site coordination and administrative activities throughout the clinical trial lifecycle.

Eligibility Criteria

Applicants should meet the following requirements:

  • Minimum 1 year of experience as a Clinical Research Coordinator (CRC).
  • Strong understanding of clinical trial processes.
  • Experience in clinical documentation and site coordination.
  • Familiarity with Good Clinical Practice (GCP) guidelines.
  • Excellent communication and coordination skills.
  • Ability to manage multiple study-related tasks efficiently.

Freshers are not eligible for this position.


Preferred Skills

  • Clinical Operations
  • Clinical Trial Documentation
  • Site Coordination
  • Good Clinical Practice (GCP)
  • Clinical Research Processes
  • Documentation Management
  • Communication Skills
  • Team Collaboration
  • Organizational Skills
  • Time Management

Salary & Benefits

  • Annual CTC: ₹2.8 – ₹4 Lakhs
  • Opportunity to work in a professional clinical research environment.
  • Exposure to clinical trial management processes.
  • Career growth in Clinical Operations and Clinical Research.
  • Hands-on experience with regulatory documentation and site coordination.
  • Collaborative and learning-focused work culture.

How to Apply

Interested and eligible candidates can send their updated resume to:

Email: hr@clinicaresearch.com

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