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Clinical Trial Assistant Jobs at Curaclin Research

Clinical Trial Assistant Jobs at Curaclin Research in Bhubaneswar for experienced candidates with regulatory, TMF, and GCP exposure.


Company Overview

Curaclin Research is an emerging clinical research organization focused on supporting ethically conducted and regulatory-compliant clinical trials in India. The organization collaborates with investigational sites, ethics committees, and sponsors to ensure clinical studies are executed in alignment with national regulations and international ICH-GCP standards. With a strong emphasis on documentation accuracy, regulatory compliance, and quality systems, Curaclin Research offers a structured environment for early-career professionals to gain hands-on experience across multiple stages of the clinical trial lifecycle. Clinical Trial Assistant Jobs


Job Location & Employment Type

  • Job Location: Bhubaneswar, Odisha
  • Employment Type: Full-Time
  • Work Mode: On-site
  • Industry: Clinical Research / CRO

Open Positions / Department Details

  • Job Title: Clinical Trial Assistant (CTA โ€“ Post 2)
  • Department: Clinical Operations / Regulatory Support
  • Experience Level: Early-career professionals

This position is suitable for candidates with prior exposure to clinical trial coordination, regulatory documentation, and ethics committee processes who wish to strengthen their career in clinical research operations. Clinical Trial Assistant Jobs


Key Roles & Responsibilities

The Clinical Trial Assistant will provide operational and regulatory support to ongoing clinical studies. The role involves close coordination with internal teams, investigational sites, and ethics committees to ensure regulatory compliance and documentation readiness. Clinical Trial Assistant Jobs

Key responsibilities include:

  • Preparing, submitting, and tracking regulatory and Ethics Committee (EC) documents
  • Supporting initial submissions, protocol amendments, continuing reviews, and study renewals
  • Maintaining and updating the Trial Master File (TMF) in accordance with ICH-GCP guidelines
  • Coordinating with clinical sites for collection and verification of essential study documents
  • Assisting in study start-up activities, including feasibility documentation and site activation readiness
  • Ensuring all regulatory documents are accurate, complete, and audit-ready
  • Tracking submission timelines and following up with ethics committees and sites
  • Supporting ongoing clinical trial maintenance activities throughout the study lifecycle
  • Assisting clinical operations teams with document control and compliance checks
  • Ensuring adherence to sponsor requirements, SOPs, and regulatory guidelines
  • Supporting internal audits, inspections, and quality reviews when required
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This role demands strong organizational skills, attention to detail, and a clear understanding of regulatory documentation processes in clinical research. Clinical Trial Assistant Jobs


Eligibility Criteria

Education

  • Bachelorโ€™s or Masterโ€™s degree in Pharmacy, Life Sciences, Biotechnology, or Clinical Research
  • Candidates with relevant academic training in clinical trials or regulatory affairs will be preferred

Experience

  • 6 months to 2 years of experience in clinical research, regulatory affairs, or clinical trial coordination
  • Exposure to TMF management, EC submissions, or study start-up activities is desirable

Skills Required

  • Practical knowledge of ICH-GCP guidelines
  • Understanding of Ethics Committee submission processes
  • Familiarity with Trial Master File (TMF) structure and maintenance
  • Strong documentation and organizational skills
  • Good written and verbal communication abilities
  • Ability to manage multiple tasks and meet regulatory timelines
  • Attention to detail with a compliance-focused mindset
  • Ability to work collaboratively with cross-functional teams

Salary & Benefits

  • Salary Range: โ‚น2,50,000 โ€“ โ‚น4,00,000 per annum (INR), based on experience and skill level

Additional benefits include structured learning, exposure to end-to-end clinical trial processes, and professional development opportunities within clinical operations and regulatory affairs. Clinical Trial Assistant Jobs


Selection Process

The selection process may include:

  1. Initial resume screening based on education and experience
  2. Technical or functional interview focusing on clinical research knowledge
  3. Evaluation of regulatory documentation and TMF understanding
  4. Final HR discussion and selection

Only shortlisted candidates will be contacted by the recruitment team. Clinical Trial Assistant Jobs


How to Apply

Interested candidates must apply via email only.

Applicants should send an updated resume highlighting clinical research experience and regulatory exposure.

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Email Subject Line:
Clinical Trial Assistant โ€“ Bhubaneswar


Important Dates

  • Application Status: Open until suitable candidates are selected

Early applications are recommended due to limited openings.


Why Apply for This Pharma Job?

This Clinical Trial Assistant position offers a valuable opportunity for early-career professionals to gain practical exposure to regulatory affairs, ethics committee coordination, and TMF management. Working with a growing clinical research organization allows candidates to understand real-world clinical trial operations beyond theory. The role supports long-term career growth in clinical operations, regulatory affairs, and project coordination, making it an ideal stepping stone for professionals aiming to build a sustainable career in clinical research. Clinical Trial Assistant Jobs


Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform created to share verified pharmaceutical and clinical research job opportunities. We are not affiliated with Curaclin Research or any hiring organization. Candidates are advised to verify job details directly with the employer before applying. IndiaPharmaJobs.in does not charge any fees for job listings or applications. Clinical Trial Assistant Jobs


Final Call-to-Action

If you have experience in clinical trial coordination and are looking to strengthen your career in regulatory affairs and clinical operations, this Clinical Trial Assistant role in Bhubaneswar offers a strong opportunity. Eligible candidates are encouraged to apply via email with their updated resumes at the earliest. Clinical Trial Assistant Jobs


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