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2 days ago
**Job Opportunity:** We are seeking a skilled Medical Writer/Clinical Study Researcher to join our team.
- Main 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.
- Craft abstracts and manuscripts, demonstrating strong scientific communication skills.
- Deliver high-quality, accurate, and well-structured documents contributing to the success of clinical research and regulatory submissions.
- Understand study objectives, design protocols, and prepare SOPs for effective documentation within timelines.
- Communicate with all stakeholders to ensure seamless documentation processes.
Requirements:
- Proficient in developing high-quality key clinical trial documents.
- Strong scientific writing and translation skills.
- Ability to work under pressure and meet deadlines.
- Familiarity with regulatory compliance guidelines.
- Excellent communication and interpersonal skills.
Benefits:
- Ongoing professional development opportunities.
- A dynamic and supportive work environment.
- The chance to contribute to impactful clinical research projects.
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