Clinical Trial Investigator

Behavioral Health Market Context

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•Must possess a PhD, MS., or similar post‑graduate degree in Science, Medicine, or Engineering
•7+ years of experience in a related field
•Must be able to effectively work and manipulate large data sets
•Experienced user in Excel and the ability to learn and adapt with various software platforms
•Well organized with a sense of responsibility for project and time management
•2 more items(s)

•The Clinical Investigator, CRS oversees the clinical research of consumer products involving healthy paid volunteers
•Develops research studies and creates standards and guidelines for clinical research services and programs
•Ensures adherence to standard operating procedures, good clinical practice and FDA regulations
•Oversees the clinical research of consumer products involving healthy paid volunteers
•Writes protocols, collects and reviews data, prepares progress reports, analyzes results, writes summaries and conclusions and issues reports
•Protects the rights, safety and welfare of subjects
•Interfaces with the Sponsor, staff, contractors, professional societies, Institutional / Investigational Review Board (IRB), subjects, government agents / agencies and other business units
•Notifies the Sponsor and / or IRB of any changes to or deviations from the protocol and document changes and deviations
•Maintains training records of staff members
•Maintains Quality Assurance (QA)
•7 more items(s)