Senior Clinical Document Specialist
2 days ago
Deliver high-quality, accurate, and well-structured clinical documents that support drug development and regulatory submissions.
- Develop key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
- Translate complex scientific data into clear, regulatory compliant documents that meet industry standards.
Proficient in developing high-quality clinical trial documents. Skilled in translating complex scientific data into clear, regulatory compliant documents. Experienced in crafting abstracts and manuscripts. Strong scientific communication skills. Proficient in MS Office Suite and Google Suite.
Benefits:Opportunity to work on high-profile projects. Collaborative and dynamic work environment. Professional growth and development opportunities. Recognition and rewards for outstanding performance.
Others:Preparation of protocols, CSRs, PIS-ICFs and CRFs. Understanding the study objectives and designing the protocol. Preparation and review of SOPs. Communicating with all stakeholders to ensure effective and complete documentation within the timeline.
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