Clinical Research Coordinator (CRC)

Company: Advent Health 

Title: Clinical Research Coordinator - RN (Oncology - GU Team)

Location: AdventHealth Cancer Institute, 2501 N Orange Ave, Orlando, FL 32804

Schedule: Onsite 5 days/week

Days: Monday - Friday

Hours: 8am - 5pm, but flex (ex: if seeing a patient at 6am, not expected to stay until 5)

Must Haves:

• 1+ year Clinical research experience
• Active RN license
• Strong foundation in Good Clinical Practice (GCP)
• Comfort working directly with oncology patients
• Strong organization and ability to coordinate across multiple clinical teams/multiple moving pieces per visit
• Interest in oncology research and patient‐centered care
• Warm personality

Plusses:

• Coordinator experience - Experience coordinating with nursing, labs, pharmacy, or imaging teams
• ACRP & SOCRA 
• Oncology Research Experience
• Bilingual

Role:

We are hiring a Clinical Research Coordinator (CRC) to support our Oncology Research Team, with a focus on patient‐centered coordination within clinical research. While this position supports the GU oncology group, the role is far more about oncology research operations than GU‐specific disease knowledge.

Oncology research can be complex- patients are seen frequently, protocols often involve multiple medications, and coordination across care teams is critical. This role is ideal for someone who enjoys working directly with patients while staying organized in a fast‐paced clinical environment.

Day-to-Day Responsibilities: 

• Coordinate and conduct patient visits for oncology clinical research studies
• Assist with screening and pre‐screening patients for clinical trials
• Partner closely with care teams to coordinate:
• Infusion appointments
• Lab draws
• Imaging visits
• Study‐specific requirements
• Communicate visit details with ancillary teams such as infusion nurses, pharmacy, lab, and imaging teams to ensure patients move smoothly through their appointments
• Help support IRB submissions and study documentation
• Track patient visits, enrollment numbers, and study schedules with strong attention to detail
• Work closely with fellow CRCs to stay aligned on shared patients and coverage

What Makes This Role Unique:

• High‐volume oncology research setting with meaningful patient interaction
• Opportunities to learn complex oncology protocols and study workflows
• Collaborative team environment with strong training support
• Hands‐on exposure to infusion‐based and drug‐intensive clinical trials

Training & Support:

• Comprehensive onboarding and training provided
• Training typically lasts 3–4 months, with continued learning up to 6 months
• You’ll be supported as you learn the protocols, workflows, and patient populations