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Senior Medical Communications Specialist
3 weeks ago
Job Overview:
The role of a Clinical Study Researcher and Medical Writer is multifaceted, requiring expertise in clinical trial documentation, scientific communication, and regulatory compliance.
- Key Responsibilities:
- Develop high-quality 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 support drug development and approval processes.
- Prepare abstracts and manuscripts, demonstrating strong scientific communication skills.
- Deliver high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
- Understand study objectives and design protocols.
- Prepare and review SOPs.
- Communicate effectively with stakeholders to ensure timely and complete documentation.
Requirements:
- Proficiency in developing high-quality clinical trial documents.
- Strong scientific communication skills.
- Ability to translate complex data into clear, regulatory compliant documents.
- Experience in crafting abstracts and manuscripts.
- Effective communication skills with stakeholders.
About This Opportunity:
This position offers a unique blend of scientific expertise and communication skills, making it an ideal fit for those who enjoy working at the intersection of science and writing. If you are passionate about medical writing and have experience in clinical trials, this could be the perfect opportunity for you.
