3 - 6 years

5 - 8 Lacs

Posted:7 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Roles and Responsibility
  • Conduct clinical trials to ensure compliance with regulatory requirements and company standards.
  • Collaborate with cross-functional teams to design, implement, and monitor clinical trial protocols.
  • Develop and maintain relationships with investigators, site staff, and other stakeholders to ensure successful study execution.
  • Review and approve clinical trial protocols, informed consent forms, and other study-related documents.
  • Ensure timely and accurate reporting of clinical trial data to relevant authorities.
  • Participate in quality assurance activities to ensure high-quality deliverables.
Job Requirements
  • Minimum 2 years of experience in clinical trials, preferably in a pharmaceutical or CRO setting.
  • Strong knowledge of Good Clinical Practice (GCP) principles and regulations governing clinical trials.
  • Excellent communication and interpersonal skills are required for effective collaboration with diverse stakeholders.
  • Ability to work independently and as part of a team to achieve study objectives.
  • Strong problem-solving skills to resolve issues during study execution.
  • Familiarity with electronic data capture systems and other clinical trial management tools.

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