Primary Duties and Responsibilities
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- Supervise a team of clinical research coordinators, providing day-to-day oversight, training, mentorship, and performance support
- Manage the full lifecycle of complex clinical trials- from study start-up through closeout ensuring compliance
- Oversee regulatory submissions, informed consent processes, patient recruitment, and data integrity
- Provide financial oversight, support budget tracking, and ensure accurate clinical trial billing and documentation
- Champion service excellence by promoting clear communication, timely issue resolution, and continuous quality improvement
- Other duties as assigned
Job Qualifications
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Bachelor’s degree in biological sciences, pharmacy, or other related field and/or equivalent combination of education and experience
Advanced Degree (preferred)
Minimum 5+ years of experience in a clinical research setting
Experience working with a variety of local and external IRBs, scientific review and other research committees
Knowledge of clinical research concepts, policies and procedures, and human safety protection regulation and laws
Clinical Research Certification (CCRP, ACRP, etc.) (preferred)
Ability to effectively communicate in a timely and professional manner
Ability to set priorities and complete ongoing tasks with competing deadlines
Proficiency with Microsoft Office Applications and Adobe