
Clinical Trial Document Specialist
4 days ago
Job Description:
We are seeking a skilled Medical Writer/Clinical Study Researcher to develop high-quality clinical trial documents that support drug development and approval processes. As a key member of our team, you will be responsible for creating clear, regulatory-compliant documents that showcase strong scientific communication skills.
The ideal candidate will have experience in developing protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs). You will also be able to translate complex scientific data into concise, well-structured documents.
Key Responsibilities:
- Developing high-quality clinical trial documents
- Translating complex scientific data into clear, regulatory compliant documents
- Crafting abstracts and manuscripts demonstrating strong scientific communication skills
- Preparing and reviewing SOPs
- Communicating with stakeholders to ensure effective and complete documentation within the timeline
Requirements:
- Proficient in developing high-quality clinical trial documents
- Strong scientific communication skills
- Able to work effectively with stakeholders
- Attention to detail and organizational skills
About Us:
We are committed to delivering high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions. If you are a skilled Medical Writer/Clinical Study Researcher looking for a challenging opportunity, we encourage you to apply.
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