Oncology Research Supervisor — Clinical Trials Team Lead

Medix™; Orlando (FL); Presencial; USD 70.000 - 112.000; Jornada completa

Descripción de la vacante

Medix is seeking an experienced Clinical Research Nurse (CRN) or Clinical Research Coordinator (CRC) with oncology research background to advance into a supervisory role. This role focuses on leading a small team, ensuring protocol compliance, and driving efficient study start-up and execution.

The candidate will mentor research staff, oversee day-to-day operations, and coordinate with sponsors and operations leadership to maintain quality and safety in oncology trials.

Formación

• 2+ years of clinical research experience with oncology focus.
• CRC or CRN background acceptable.
• Experience mentoring, training, or leading research staff.

Responsabilidades

• Oversee day-to-day activities of the clinical research team; manage workflow, staffing, and study priorities.
• Provide guidance, mentorship, training, and support to team members.
• Serve as resource for operational barriers; improve research processes and SOPs.
• Support onboarding, preceptorship, and performance management.
• Promote a positive team environment through regular communication.
• Ensure quality, participant safety, and regulatory compliance in operations.
• Coordinate oncology protocols from start-up to study completion.
• Partner with leadership, study intake, and sponsors to support start-up and execution.
• Monitor supplies and inventory; identify workflow improvement opportunities.

Conocimientos

Leadership

Mentoring

Team leadership

Organizational skills

Communication

Problem-solving

Educación

RN license

Descripción del empleo

Medix is seeking an experienced Clinical Research Nurse (CRN) or Clinical Research Coordinator (CRC) with oncology research background to advance into a supervisory role. This role focuses on leading a small team, ensuring protocol compliance, and driving efficient study start-up and execution.

The candidate will mentor research staff, oversee day-to-day operations, and coordinate with sponsors and operations leadership to maintain quality and safety in oncology trials.