Clinical Trial Assistant @ Dhanraj Construction

Job Description

TMF Specialist

Responsibilities:

• Receive and process clinical trial documents, ensuring proper filing and indexing.
• Perform quality checks on documents to ensure they meet regulatory requirements and study protocols.
• Maintain and update the TMF according to established guidelines and best practices.
• Track and manage document versions and ensure timely filing of essential documents.
• Respond to requests for documents from internal and external stakeholders.
• Prepare the TMF for inspections and audits.
• Collaborate with cross-functional teams, including clinical research associates, data managers, and regulatory affairs specialists.
• Stay up-to-date on evolving TMF regulations and best practices.

Qualifications:

• Bachelor's degree in life sciences, healthcare administration, or a related field preferred.
• Minimum of 0-2 years of experience in clinical research or document management.
• Strong understanding of Good Clinical Practice (GCP) guidelines and TMF regulations.
• Excellent organizational and time management skills.
• Proficiency in Microsoft Office Suite and document management systems.
• Meticulous attention to detail and accuracy.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.

Interested to apply can share Cv or call/whatsapp to hidden_mobile 
 

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Pharmacist / Medical Representative
Functional Area: Not Applicable
Role/Responsibilies: Clinical Trial Assistant

+ View Contact

Keyskills:   clinical documentation document management regulatory affairs gcp tmf healthcare administration clinical research clinical trials