Associate Clinical Research Coordinator

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 30,000 - 46,000; Full time

Benefits offered by this job

Relocation assistance

CTO Academy training

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator Associate to support non-therapeutic and therapeutic studies, coordinate data collection, obtain informed consent, and liaise with study teams. This entry-level to mid-career position offers a clear career path within the Clinical Trials Office and related departments.

The role features a Monday–Friday schedule with hybrid work after a 90‑day training period, relocation assistance possibly available, and paid training through the

Qualifications

• Associate’s degree required or 2 years of relevant experience with a high school diploma or GED
• Bachelor’s degree preferred in scientific, health related or business administration program
• Experience in clinical trials or regulatory requirements is preferred

Responsibilities

• Assist with informed consent and enrollment of study participants
• Coordinate data entry and study-related activities across protocols
• Support regulatory documentation and communication with study sponsors
• Assist with specimen collection and data monitoring as needed

Skills

Effective communication

Teamwork

Education

Associate degree

Bachelor’s degree 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.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-administrationClinical TrialsThese 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.Successful candidates will possess:Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skillsExcellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiencesPrior experience in clinical trials is preferredFamiliarity with regulatory requirements in clinical research or ability to successfully learn thisExperience interacting with patients and coordinating care with medical staffGain a solid learning and understanding of regulatory guidelines and following a clinical trial protocolPosition Highlights:The Clinical Research Coordinator Associate is a support position that administers duties related to the collection of data and/or the coordination of clinical trials, at Moffitt Cancer Center. Activities support assigned research protocols and include the coordination activities of assigned research protocols (generally non-therapeutic in nature) including obtaining informed consent from study participants, specimen collection and data entry.The job is a pre-entry position for the Clinical Trials Coordinator career path or other medical or research career paths.Other job duties may include support of therapeutic studies including completion of data entry into various database systems, follow-up of patients according to protocol (via review of records, clinic visit or telephone call), ordering supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, communicating with study sponsors, and facilitating the collection of study-required specimens.The position applies job skills and company policies and procedures to complete assigned tasks. Within its administrative support duties, it receives moderate supervision. The assignments are semi-routine in nature, but the CRC Associate recognizes the need for occasional deviation from accepted practice. Requires instructions only on new assignments.Credentials and Qualifications:*Associate’s degree*In lieu of an associate’s degree, 2 years of relevant experience required with a high school diploma or GEDBachelor’s degree preferred in scientific, health related or business administration program.Salary Range$21.65 - $33.05Salary 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