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Jd For Clinical Study Design_mbbs_hyderabad @ randstad offshore

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 Jd For Clinical Study Design_mbbs_hyderabad

Job Description

Role & responsibilities :


Key Responsibilities

  • Conduct medical review of study related documents
  • Prepare high quality medical rationale documents for agency submission
  • Periodic Safety review
  • Medical monitoring
  • Develop clinical rationale for new products.

Competencies and exposure to succeed in the role.

  • Previous experience in medical review of clinical study documents (trial and BA/BE).
  • Knowledge of clinical development for different regulatory such as USFDA, IND, EMA, JFDA.
  • Familiarity with medical coding dictionaries (e.g., MedDRA) and safety reporting
  • Strong attention to detail and ability to work with complex medical data.
  • Effective communication and interpersonal skills to collaborate with cross-functional teams and stakeholders.

Preferred candidate profile

Job Classification

Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Research & Development
Role Category: Pharmaceutical & Biotechnology
Role: Clinical research Scientist
Employement Type: Full time

Contact Details:

Company: randstad offshore
Location(s): Hyderabad

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Keyskills:   Literature Search Clinical Development Clinical Trials Protocol Writing medical reviwer

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₹ 6-13 Lacs P.A

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