AdventHealth
Clinical Research Coordinator II Oncology
Join AdventHealth as a Clinical Research Coordinator II (Oncology) at the Winter Park Cancer Center (2100 Glenwood Drive, Ste 201). This full‑time, day shift role is based in Winter Park, Florida.
Benefits
Benefits from Day One
Paid Days Off from Day One
Student Loan Repayment Program
Career Development
Whole Person Well‑Being Resources
Mental Health Resources and Support
Pet Insurance
Schedule & Location Schedule:
Full time Shift:
Day Location:
Winter Park Cancer Center, 2100 Glenwood Drive Ste 201, Winter Park, FL
Community AdventHealth Orlando, a flagship 1,368‑bed hospital serving the Southeast, Caribbean, and South America, provides a vibrant environment for clinical research and patient care.
Role Overview The Clinical Research Coordinator II serves the AdventHealth Research Institute (AHRI) by planning, coordinating, evaluating, and performing nursing care for participants while collecting data for assigned research projects. The role follows study‑specific protocol guidelines, communicates with Principal Investigators (PI), Sub‑Investigators, Clinical Research Leads, and support staff, and ensures compliance with FDA, ICH/GCP, and HIPAA regulations.
Responsibilities
Advocate for patients while conducting industry‑sponsored and investigator‑initiated clinical trials.
Review and explain informed consent documents to participants and legal representatives.
Manage multiple trial protocols, coordinate execution and follow‑up, and maintain accurate, legible documentation.
Adhere to hospital policies, SOPs, and all applicable local, state, and federal regulations.
Coordinate support staff, laboratory technicians, and assistants to ensure timely, high‑quality results.
Serve as liaison between PIs, IRB, and Office of Sponsored Programs; prepare and review all required study documentation.
Collaborate with sponsors and assist site monitors during visits.
Provide flexible hours and availability for research‑related questions.
Perform additional duties as assigned to support smooth operations of the AHRI Core.
Qualifications
Bachelor’s degree and at least 2 years of clinical research experience, OR
Associate’s degree and at least 4 years of experience, OR
Graduate of an accredited allied health certificate program with six (6) years of clinical research or healthcare experience.
Preferred: Master’s degree in Healthcare, Research, or related field.
Certification as Clinical Research Coordinator (CCRC) (ACRP or SOCRA).
American Heart Association BLS, ACLS, or other relevant certifications.
Additional certifications such as medical assistant, medical technician, or phlebotomy are advantageous.
EEO Statement This facility is an equal opportunity employer and complies with federal, state, and local anti‑discrimination laws, regulations, and ordinances. We do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age, or disability/handicap in respect to recruitment, selection, placement, promotion, wages, benefits, and other terms and conditions of employment.
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Benefits
Benefits from Day One
Paid Days Off from Day One
Student Loan Repayment Program
Career Development
Whole Person Well‑Being Resources
Mental Health Resources and Support
Pet Insurance
Schedule & Location Schedule:
Full time Shift:
Day Location:
Winter Park Cancer Center, 2100 Glenwood Drive Ste 201, Winter Park, FL
Community AdventHealth Orlando, a flagship 1,368‑bed hospital serving the Southeast, Caribbean, and South America, provides a vibrant environment for clinical research and patient care.
Role Overview The Clinical Research Coordinator II serves the AdventHealth Research Institute (AHRI) by planning, coordinating, evaluating, and performing nursing care for participants while collecting data for assigned research projects. The role follows study‑specific protocol guidelines, communicates with Principal Investigators (PI), Sub‑Investigators, Clinical Research Leads, and support staff, and ensures compliance with FDA, ICH/GCP, and HIPAA regulations.
Responsibilities
Advocate for patients while conducting industry‑sponsored and investigator‑initiated clinical trials.
Review and explain informed consent documents to participants and legal representatives.
Manage multiple trial protocols, coordinate execution and follow‑up, and maintain accurate, legible documentation.
Adhere to hospital policies, SOPs, and all applicable local, state, and federal regulations.
Coordinate support staff, laboratory technicians, and assistants to ensure timely, high‑quality results.
Serve as liaison between PIs, IRB, and Office of Sponsored Programs; prepare and review all required study documentation.
Collaborate with sponsors and assist site monitors during visits.
Provide flexible hours and availability for research‑related questions.
Perform additional duties as assigned to support smooth operations of the AHRI Core.
Qualifications
Bachelor’s degree and at least 2 years of clinical research experience, OR
Associate’s degree and at least 4 years of experience, OR
Graduate of an accredited allied health certificate program with six (6) years of clinical research or healthcare experience.
Preferred: Master’s degree in Healthcare, Research, or related field.
Certification as Clinical Research Coordinator (CCRC) (ACRP or SOCRA).
American Heart Association BLS, ACLS, or other relevant certifications.
Additional certifications such as medical assistant, medical technician, or phlebotomy are advantageous.
EEO Statement This facility is an equal opportunity employer and complies with federal, state, and local anti‑discrimination laws, regulations, and ordinances. We do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age, or disability/handicap in respect to recruitment, selection, placement, promotion, wages, benefits, and other terms and conditions of employment.
#J-18808-Ljbffr