Moffitt Cancer Center
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CLINICAL RESEARCH COORDINATOR II
role at
Moffitt Cancer Center
Summary Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan.
Position Highlights
Supports the Principal Investigator (PI) in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center.
As the primary resource for the protocols, the CRC II will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines.
Will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor.
Along with the investigator, the CRC II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
The CRC II will perform all Clinical Research Coordinator core support and additional responsibilities of more complex studies, with a higher patient volume.
The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies.
Credentials And Qualifications
Bachelor’s degree with 2 years clinical trials coordination experience
In lieu of a bachelor’s degree, an associate’s degree with 4 years clinical trials coordination experience may be considered
CCRP/CCRC certification preferred.
Seniority level Entry level
Employment type Full-time
Job function Research, Analyst, and Information Technology
Industries Hospitals and Health Care
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CLINICAL RESEARCH COORDINATOR II
role at
Moffitt Cancer Center
Summary Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan.
Position Highlights
Supports the Principal Investigator (PI) in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center.
As the primary resource for the protocols, the CRC II will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines.
Will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor.
Along with the investigator, the CRC II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
The CRC II will perform all Clinical Research Coordinator core support and additional responsibilities of more complex studies, with a higher patient volume.
The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies.
Credentials And Qualifications
Bachelor’s degree with 2 years clinical trials coordination experience
In lieu of a bachelor’s degree, an associate’s degree with 4 years clinical trials coordination experience may be considered
CCRP/CCRC certification preferred.
Seniority level Entry level
Employment type Full-time
Job function Research, Analyst, and Information Technology
Industries Hospitals and Health Care
#J-18808-Ljbffr