Top Clinical Trials Manager
2 semanas atrás
Senior Clinical Research Associate
We are seeking a highly skilled and experienced professional to manage clinical trials from start to finish, ensuring the highest level of quality and adherence to regulatory requirements.
Key Responsibilities:- Serve as primary contact for assigned study sites, conducting site visits and completing deliverables with quality and within given timelines.
- Assist with or oversee study start-up activities, including feasibility assessments, pre-study preparations, and site selection processes.
- Collect, review, and track essential/regulatory documents, ensuring accurate and compliant data management.
- Participate in investigator, client, and project team meetings, facilitating effective communication and collaboration.
- Ensure proper storage, dispensation, and accountability of all Investigational Product (IP) and trial-related materials, adhering to established protocols.
- 3+ years of clinical trial monitoring experience or equivalent experience, demonstrating a strong foundation in clinical research principles.
- Bachelor's Degree or higher in an allied health field, showcasing academic excellence and relevant coursework.
- Previous experience in conducting clinical research studies in a hospital setting, pharmaceutical company, or Contract Research Organization (CRO), highlighting adaptability and versatility.
- Opportunity to work on high-profile clinical trials, contributing to groundbreaking research and advancements in healthcare.
- Collaborative and dynamic work environment, fostering growth, learning, and professional development.
- Comprehensive training and mentorship programs, providing ongoing support and guidance.
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