
Clinical Documentation Specialist
3 days ago
Job Title: Clinical Documentation Specialist
">- Responsible for developing high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
- Skilled in translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
- Experienced in crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
- Committed to delivering accurate and well-structured documents that contribute to the success of clinical research and regulatory submissions.
Key Responsibilities:
">- Preparation and review of SOPs.
- Communication with all stakeholders to ensure effective and complete documentation within the timeline.
- Understanding the study objectives and designing the protocol.
Requirements:
">- Proficient in MS Office Suite.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
Benefits:
">- Opportunity to work on challenging projects.
- Collaborative and dynamic work environment.
- Professional growth and development opportunities.
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