Curaclin Hiring Clinical Trial Assistants
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Core Competencies:
- Eligibility / Qualifications
- Required Education:
- Experience:
- Key Skills:
- Location & Salary
- Job Location:
- Salary:
- Application Process
- Apply via Email:
- Why This Role Matters in Clinical Research
- Frequently Asked Questions (FAQs)
- 1. Who can apply for the CTA role?
- 2. Is prior TMF experience required?
- 3. What is the work profile of a CTA?
- 4. Is this role suitable for freshers?
- 5. What are the growth opportunities?
- Summary
Curaclin Research is hiring Clinical Trial Assistants (CTA) with 2 open positions for candidates with 6 months to 2 years of experience in clinical research operations. This opportunity is based in Bhubaneswar, Odisha and is ideal for early-career professionals looking to build expertise in regulatory documentation, Trial Master File (TMF) management, and study start-up activities. While not a pure fresher role, candidates with internship or short-term experience in clinical trials, GCP compliance, and site coordination are strongly encouraged to apply.
Company Overview
Curaclin Research is a Site Management Organization (SMO) focused on delivering efficient clinical trial execution across sites. The company supports sponsors and CROs with study start-up, regulatory submissions, ethics committee coordination, and site operations aligned with ICH-GCP standards.
With increasing demand for clinical trials in India, Curaclin plays a key role in accelerating study timelines while maintaining strict compliance with global regulatory frameworks. The organization emphasizes data integrity, patient safety, and audit-ready documentation, making it a strong platform for professionals aiming to grow in clinical research, pharmacovigilance, and regulatory operations.
Job Role & Responsibilities
As a Clinical Trial Assistant, you will support study start-up and ongoing trial activities, focusing on documentation quality, regulatory submissions, and coordination with investigative sites.
Key Responsibilities:
- Handle Regulatory Authority and Ethics Committee (EC) documentation, submissions, tracking, and follow-ups
- Maintain and update Trial Master File (TMF) in line with sponsor requirements, ICH-GCP, and regulatory guidelines
- Coordinate with investigational sites for timely collection and verification of essential documents
- Support study start-up activities including site feasibility, document collection, and activation readiness
- Assist with submissions, amendments, and renewals as per protocol and regulatory timelines
- Ensure documentation accuracy, version control, and audit readiness
- Track milestones and maintain logs for submissions and approvals
- Collaborate with clinical operations, quality, and regulatory teams to ensure compliance
Core Competencies:
- Understanding of clinical trial lifecycle and study start-up processes
- Working knowledge of ICH-GCP guidelines and regulatory documentation
- Familiarity with TMF structure, filing, and maintenance
- Strong attention to detail and documentation accuracy
Eligibility / Qualifications
Required Education:
B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Clinical Research, Biotechnology, Microbiology, Biochemistry)
Experience:
- 6 months to 2 years in clinical research, SMO/CRO operations, or site coordination
- Exposure to TMF management, EC submissions, or regulatory documentation preferred
Key Skills:
- Knowledge of ICH-GCP and clinical research regulations
- Documentation and file management skills (TMF/eTMF exposure is a plus)
- Coordination and stakeholder communication skills
- Ability to manage timelines and maintain compliance
Location & Salary
Job Location:
Bhubaneswar, Odisha
Salary:
Competitive, based on experience in clinical operations, TMF management, and regulatory submissions. Candidates with hands-on exposure to study start-up and EC coordination can expect better compensation aligned with market standards.
Application Process
Interested candidates can apply by sharing their updated CV via email. Highlight your experience in TMF handling, EC submissions, and clinical documentation to improve shortlisting chances.
Apply via Email:
Why This Role Matters in Clinical Research
Clinical Trial Assistants are central to maintaining compliance and documentation integrity in trials. Accurate TMF management and timely regulatory submissions directly influence study approvals, site activation, and audit outcomes.
This role contributes to faster clinical development and ensures that investigational therapies reach patients safely. With growing clinical research activity in India, CTA roles offer strong career progression into Clinical Research Associate (CRA), Regulatory Affairs, and Clinical Operations.
Frequently Asked Questions (FAQs)
1. Who can apply for the CTA role?
Candidates with life sciences or pharmacy degrees and 6 months to 2 years of clinical research experience can apply.
2. Is prior TMF experience required?
Preferred but not mandatory. Basic understanding of TMF structure and GCP is important.
3. What is the work profile of a CTA?
Handling regulatory and EC submissions, maintaining TMF, coordinating with sites, and supporting study start-up and ongoing trial activities.
4. Is this role suitable for freshers?
Strict freshers are not targeted, but candidates with internships or short-term exposure to clinical research may be considered.
5. What are the growth opportunities?
Progression to CRA, Clinical Operations Specialist, or Regulatory Affairs roles based on performance and experience.
Summary
| Company | Curaclin Research |
|---|---|
| Vacancies | Clinical Trial Assistant (CTA) – 2 Positions |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Clinical Research, Biotechnology, Microbiology, Biochemistry) |
| Experience | 6 Months – 2 Years in Clinical Research / SMO / CRO |
To apply for this job please visit curaclinsmo.com.
