CLINICAL RESEARCH COORDINATOR II

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 40,000 - 61,000; Full time

Job summary

Moffitt Cancer Center in Tampa is seeking a dedicated Clinical Research Coordinator (CRC II) to support clinical trials by coordinating patient care and regulatory processes, enrolling and following study subjects, and liaising with investigators and study sponsors.

This role offers a Monday–Friday schedule with a hybrid work arrangement after a 90-day introductory period, and a salary range reflecting clinical trials experience. Career growth and CCRP/CCRC opportunities are available.

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.

Responsibilities

• Coordinate research including administrative procedures at Moffitt Cancer Center.
• Screen, enroll, and follow study subjects with protocol compliance.
• Serve as liaison between investigators, care providers, and sponsor/regulatory staff.
• Provide core clinical research coordinator support for complex studies with higher patient volume.

Skills

Clinical trials coordination

Regulatory knowledge

Education

Bachelor’s degree

Associate’s degree

CCRP/CCRC certification preferred

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.SummaryJob 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.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 consideredCCRP/CCRC certification preferred.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