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Senior Clinical Study Research Specialist
3 weeks ago
Clinical Study Researcher Opportunity
- Job Description: We are seeking a skilled Clinical Study Researcher to join our team. As a key member of our research team, you will be 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).
- Required Skills and Qualifications: Proficient 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 high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
- Benefits: This role offers a unique opportunity to work on a variety of projects, develop your skills, and make a meaningful contribution to the success of our organization.
Responsibilities include preparation and review of SOPs, communicating with stakeholders to ensure effective and complete documentation within the timeline, and understanding study objectives and designing protocols.
Why Join Us:
- Develop your skills and expertise in clinical research
- Contribute to the success of our organization
- Work on a variety of projects and challenges
