Curaclin Research Hiring Clinical Trial Assistants

Clinical Trial Assistant Vacancies at Curaclin Bhubaneswar

Curaclin Research hiring Clinical Trial Assistants with 6 months–2 years experience in Bhubaneswar, Odisha. CTA openings available.

Curaclin Research has announced hiring for the position of Clinical Trial Assistant (CTA) at its Bhubaneswar, Odisha location. This opportunity is designed for early-career clinical research professionals who want hands-on exposure to regulatory operations, ethics committee coordination, and trial documentation in a GCP-compliant clinical research environment. Candidates with 6 months to 2 years of relevant experience will find this role well suited for building a strong foundation in clinical trials and regulatory affairs.

Company Overview

Curaclin Research is a growing clinical research organization focused on delivering high-quality clinical trial support services across multiple therapeutic areas. The organization operates with a strong emphasis on regulatory compliance, ethical research practices, and adherence to international clinical research standards such as ICH-GCP. Curaclin Research supports sponsors and investigators through efficient trial management, documentation control, and site coordination.

The company’s work directly contributes to the development of safe and effective healthcare solutions by ensuring clinical trials are conducted ethically, accurately, and in compliance with regulatory expectations. Professionals working at Curaclin Research gain practical exposure to real-world clinical trial operations, making it an ideal environment for career growth in clinical research and regulatory affairs.

Job Role & Responsibilities

Clinical Trial Assistant (CTA)

The Clinical Trial Assistant will support clinical operations teams throughout the lifecycle of clinical studies, from start-up activities to ongoing trial maintenance.

Key Responsibilities:

• Handling regulatory and Ethics Committee (EC) documentation, submissions, tracking, and follow-ups
• Preparation, submission, and maintenance of regulatory documents as per protocol requirements
• Maintaining and updating the Trial Master File (TMF) in compliance with sponsor requirements, ICH-GCP, and regulatory guidelines
• Coordinating with investigational sites for timely collection and verification of essential documents
• Assisting with study initiation and start-up activities, including site feasibility and activation readiness
• Supporting protocol amendments, renewals, and ongoing regulatory submissions
• Ensuring accuracy, completeness, and audit readiness of trial documentation
• Supporting internal teams during inspections, audits, and sponsor reviews

This role provides strong exposure to regulatory operations, documentation control, and site coordination, which are critical skill areas in clinical research careers.

Eligibility / Qualifications

Required Education

• Life Sciences Graduate or Postgraduate

Relevant Courses Include:
B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Clinical Research, Pharmacy, Biomedical Sciences

Experience Requirement

• 6 months to 2 years of experience as a Clinical Trial Assistant, Clinical Research Coordinator, or in clinical operations support
• Working knowledge of ICH-GCP guidelines and clinical trial documentation
• Familiarity with regulatory submissions and Ethics Committee processes is preferred

Location & Salary

Job Location:
Bhubaneswar, Odisha

Salary Package:
Salary will be competitive and commensurate with experience, skills, and interview performance. Entry-level clinical research professionals can expect industry-aligned compensation.

Application Process

Interested candidates can apply by sharing their updated resume via email.

Apply Here: Shr.curaclinresearch@gmail.com

Candidates are advised to mention “Clinical Trial Assistant – Bhubaneswar” in the email subject line for faster shortlisting.

Why Join Curaclin Research

• Direct exposure to clinical trial regulatory and documentation activities
• Strong learning environment for early-career clinical research professionals
• Experience working with ICH-GCP compliant systems
• Opportunity to build long-term career paths in clinical operations and regulatory affairs
• Contribution to ethical and compliant clinical research that advances healthcare

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Frequently Asked Questions (FAQs)

Who can apply for the Clinical Trial Assistant role?

Candidates with life sciences or pharmacy backgrounds and 6 months to 2 years of clinical research experience can apply.

Is this role suitable for freshers?

Candidates with internship or short-term experience in clinical research are eligible.

What are the key skills required for this role?

Knowledge of ICH-GCP, regulatory documentation, TMF maintenance, and site coordination is required.

What is the job location?

The position is based in Bhubaneswar, Odisha.

How do I apply for this job?

Candidates should email their updated resume to Shr.curaclinresearch@gmail.com.

Summary Table

Company	Curaclin Research
Vacancies	Clinical Trial Assistant (CTA)
Required Education	B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Clinical Research
Experience	6 Months to 2 Years