Curaclin Research Hiring For Clinical Trial Assistant

Pharmabharat; Hinoba-an; On-site; PHP 198,000 - 297,000; Full time

Job summary

Curaclin Research is hiring Clinical Trial Assistants (CTA) for its operations in Bhubaneswar. The role focuses on regulatory documentation, EC submissions, and TMF maintenance, with 1–2 years of experience preferred.

Selected candidates will support trial start-up activities, site coordination, and regulatory submissions in a fast-paced clinical research environment.

Qualifications

• 1–2 years of relevant clinical research or trial operations experience.
• Experience or exposure to regulatory documentation and Ethics Committee submissions.
• Understanding of Trial Master File (TMF) processes and GCP/ICH guidelines.

Responsibilities

• Handle Regulatory and Ethics Committee (EC) documentation, submissions, tracking and follow-ups.
• Maintain TMF according to sponsor requirements and GCP/ICH guidelines.
• Coordinate with investigational sites to ensure timely collection of essential documents.
• Support study initiation and start-up activities, including site feasibility and activation readiness.
• Assist with regulatory submissions, amendments and renewals as per protocol requirements.
• Track documentation and follow up with stakeholders to support study progress.

Skills

Regulatory docs

EC submissions

TMF management

GCP/ICH

Site coordination

Documentation

Job description

Curaclin Research Hiring For Clinical Trial Assistant

B.Pharm / M.Pharm / Pharm.D / B.Sc / M.Sc

Bhubaneswar, Odisha

1–2 Years

Verified Job

Email Application

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Curaclin Research is hiring Clinical Trial Assistants (CTA) for its clinical research operations in Bhubaneswar, Odisha. The company has 2 openings for candidates with 1–2 years of experience who can support regulatory documentation, Ethics Committee submissions, Trial Master File (TMF) maintenance, and clinical trial site start-up activities.

This Clinical Trial Assistant job in Bhubaneswar is a suitable opportunity for professionals looking to build or advance their careers in clinical research and clinical trial operations.

Curaclin Research Clinical Trial Assistant Jobs 2026

Clinical Trial Assistant Responsibilities

Selected candidates will support clinical trial activities, documentation, and study start-up operations. Key Clinical Trial Assistant responsibilities include:

• Handle Regulatory and Ethics Committee (EC) documentation, submissions, tracking, and follow-ups.
• Maintain and update the Trial Master File (TMF) according to sponsor requirements and applicable GCP and ICH guidelines.
• Coordinate with investigational sites to ensure timely collection of essential documents.
• Support study initiation and start-up activities, including site feasibility, document collection, and activation readiness.
• Assist with regular regulatory submissions, amendments, and renewals according to protocol requirements.
• Track documentation and follow up with relevant stakeholders to support timely study progress.
• Help ensure clinical trial documentation remains complete, accurate, and inspection-ready.

Clinical Trial Assistant Eligibility

Candidates applying for this CTA vacancy in Bhubaneswar should have:

• 1–2 years of relevant experience in clinical research or clinical trial operations.
• Experience or exposure to regulatory documentation and Ethics Committee submissions.
• Understanding of Trial Master File (TMF) processes.
• Familiarity with GCP and ICH guidelines.
• Ability to coordinate with clinical research sites and study teams.
• Good documentation, communication, organization, and follow-up skills.

Note: The provided job advertisement does not specify a particular educational qualification. Candidates should confirm the required degree/qualification with Curaclin Research before applying.

Why Consider This Clinical Research Opportunity?

This role provides exposure to several important areas of clinical research, including:

• Clinical trial start-up and site activation
• Regulatory and Ethics Committee submissions
• Site documentation and coordination
• GCP/ICH-compliant clinical trial documentation
• Study amendments and renewals

For professionals with relevant experience, this Clinical Trial Assistant career opportunity in Bhubaneswar can provide practical exposure across multiple clinical trial functions.