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Clinical Trial Analyst

0.00 to 2.00 Years   Delhi   13 Feb, 2024
TECHNO ENDURA
Job LocationDelhi
EducationNot Mentioned
SalaryRs 4.0 - 6 Lakh/Yr
IndustryMedical / Healthcare
Functional AreaPharmacist / Medical Representative
EmploymentTypeFull-time

Job Description

    TMF SpecialistResponsibilities:
    • 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:
    • Bachelors 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

Keyskills :
healthcare administrationgcpclinical documentationregulatory affairsclinical trialstmfdocument management

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