Clinical Research Coordinator II - GYN

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 4,002,000 - 6,100,000; Full time

Job summary

Moffitt Cancer Center in Tampa is seeking a Clinical Research Coordinator II to support investigators in running cancer trials. You will screen, enroll and follow study subjects, educate patients, and help ensure protocol compliance while coordinating with physicians, nurses, and sponsors.

This development role offers a hybrid schedule after a 90-day introductory period, with paid training through the CTO Academy and opportunities to advance as you gain experience in Good Clinical Practices and

Qualifications

• Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred.
• Two (2) years of clinical trials coordination experience.
• Associate's degree considered with two (2) additional years of experience.
• Proficiency in EMR systems, trial management systems, and data capture/reporting systems.

Responsibilities

• Coordinate patient care and enroll/monitor study subjects per protocol.
• Collaborate with medical staff and sponsor for regulatory compliance.
• Manage multiple studies with increasing scope and data capture.

Skills

EMR systems

Clinical trial management systems

Microsoft Office

Database entry

GCP knowledge

Medical terminology

Verbal and written communication

Education

Bachelor's degree in scientific/health/business administration

Tools

CCRP/CCRC

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.SummaryAre 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.Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career.This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided.https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administrationThese positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers.Clinical Research Coordinator IIPosition Highlights:The Clinical Research Coordinator II (CRC II) is a second level in the CRC career path within Clinical Trials. It is a development career position supporting the PI in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center. The CRC II may also support PI sponsored IND or IDE trials. 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. The CRC II 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 CRC core support and additional responsibilities of more complex studies, with a higher patient volume in comparison to the CRC I. The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies. The supervisor or Principal Investigator will provide more detailed instructions on new complex assignments where there is limited prior depth, or breadth of knowledge or working experience. Moderate supervision provided while developing latitude for independent judgment. Still developing and acquiring higher level knowledge and skills, while working on moderate scope complexity where analysis of situations or data requires a review of a variety of factors. Solves a range of straight forward problems using prescribed guidelines and policies. Limited problem solving while working under defined guidelines. Continues to build productive internal/external working relationships.Requirements:Education and Experience:Bachelor's degree with a concentration in a scientific, health related, or business administration program preferredTwo (2) years of clinical trials coordination experience.Associate's degree considered with two (2) additional years of experience.License/Certification:CCRP/CCRC or equivalent preferredKnowledge and Skills:The CRC II is required to have thorough knowledge of word processing (Microsoft Office Suite), data base entry, and thorough knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research. They should be proficient in the use of EMR systems, clinical trial management systems and various other data capture/reporting systems. This person must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals. A proficient understanding of medical terminology required. The CRC II is required to work under minimal supervision to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing. The ability to prioritize assignments and pace one’s-self when working under the pressure of deadlines and work volume is required. This person must successfully demonstrate competency by meeting established competency guideline/checklist annually.Salary Range$29.05 - $44.28Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.Moffitt Career SiteIf you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!1. Equal Employment OpportunityMoffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.2. Reasonable AccommodationFederal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at [e-mail]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.Read more information about your EEO rights under the law.Transparency in Coverage Rule