Senior Assistant Clinical Research

We are looking for a highly skilled and experienced Senior Assistant Clinical Research to join our team at Fortis Healthcare Ltd. The ideal candidate will have a strong background in clinical research and a passion for delivering exceptional results.

Roles and Responsibility

  • Assist in the development and implementation of clinical research protocols and study designs.
  • Coordinate with cross-functional teams, including data management, biostatistics, and medical writing.
  • Conduct literature reviews and analyze data to inform study design and methodology decisions.
  • Develop and maintain databases and tracking systems for clinical trial data.
  • Collaborate with investigators and site staff to ensure compliance with study protocols and regulations.
  • Prepare and review study-related documents, including protocols, informed consent forms, and case report forms.

Job Requirements

  • Bachelor's degree in a related field such as biology, pharmacy, or medicine.
  • Proven experience in clinical research, preferably in a pharmaceutical company or CRO setting.
  • Strong knowledge of Good Clinical Practice (GCP) principles and regulatory requirements.
  • Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.
  • Proficiency in statistical analysis software and database management systems.
  • Ability to prioritize tasks and manage multiple projects in a fast-paced environment.
Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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