Clinical Research Associate Manager
1 week ago
This is an exceptional opportunity for Clinical Research Associates to excel in their careers. At Pharma Universe, we offer a dynamic work environment where CRAs can monitor an average of 6 visits per month, allowing them to decide which sites can be monitored remotely and which will require an in-person visit.
Key Responsibilities- Create and implement subject enrolment strategies for assigned investigative sites
- Conduct study site visits (pre-study, initiation, monitoring, and close-out) and complete site visit deliverables within given timelines in the Monitoring Plan
- Ensure proper storage, dispensation, and accountability of all investigational product(s) and trial-related material
- Participate and act as Lead CRA on studies where they can add value
- Maintain tracking records for assigned sites including tracking of subject status, subject case report form (CRF) retrieval / source document review (SCV), regulatory documents, and investigational product
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase I and/or II is preferred
- Oncology and Rare Disease experience is highly desirable
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Ability to travel
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Clinical Research Associate
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Clinical Trials Specialist
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Research Associate
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