Clinical Research Site Manager
1 month ago
About the Role:
The Clinical Research Manager will be responsible for overseeing the day-to-day clinical operations at our site, ensuring the optimal conduct of studies, maintaining protocol compliance, and meeting clinical data quality standards.
Key Responsibilities:
- Directly manage site staff, including interviews, training, performance reviews, and goal performance oversight.
- Manage staffing needs, develop and refine subject visit flow, and ensure on-time data capture by delegated staff.
- Track vital trial metrics and operational objectives, ensuring conformance to laws, regulations, GCP guidelines, protocol, and internal SOPs/policies.
- Participate in the conduct of PSSVs, SIVs, and introduce self to CROs, Project Managers, and CRAs.
- Provide backup for study tasks, maintain oversight of accurate and efficient data entry, and address patient, vendor, and sponsor complaints.
- Facilitate the Quality Control process.
Requirements:
- Bilingual Spanish/English (or comfortable discussing complex medical terms with patients and vendors).
- 5+ years of Clinical Research experience at the site level.
- 1+ years of direct people management experience.
- Willingness to jump in hands-on as a CRC as needed.
About SQRL:
SQRL is a fast-growing clinical research site network with over 10 sites, managing clinical studies in Phase I - IV in therapeutic areas mainly focused on GI, Hepatology, and CNS. Our goal is to be the best place to work in the country, and we're excited to find people who share our vision.
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