Clinical Research Supervisor
1 month ago
Job Title: Clinical Research Supervisor
M-F schedule - day shift - onsite in Orlando
Job Description
The Clinical Research Supervisor provides oversight of the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations, and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines. The Supervisor functions as a clinical study coordinator and assists in mentoring and developing clinical study coordinators and research staff. Responsibilities include scheduling clinical operations, supervising day-to-day activities, maintaining clinical competencies, and ensuring compliance with HIPAA regulations. The Supervisor will also manage clinical space, inventory, and supplies, and collaborate with Core Managers to optimize workflow and scheduling.
Hard Skills
- physical assessment
- phlebotomy
- IV insertion
- clinical research coordination
- development of SOPs
Soft Skills
- mentoring
- supervision
- performance management
- collaboration
- organization
Work Environment
Work environment includes both inpatient and outpatient clinical settings within the campus.
For more information, reach out to Gavin Pacheco - gpacheco@
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email ) for other accommodation options.
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