Associate Clinical Research Coordinator-Breast

Moffitt; Town of Florida (NY); Hybrid; USD 30,000 - 46,000; Full time

Job summary

At Moffitt Cancer Center in Florida, the Associate Clinical Research Coordinator-Breast supports data collection, patient coordination, and regulatory tasks within clinical trials. The role combines remote and on-site work, with a 90-day training period and opportunities for growth in the Clinical Trials Office Academy.

The ideal candidate has an associate degree or equivalent experience, strong communication, and teamwork skills, plus familiarity with clinical research processes and patient

Qualifications

• Associate's degree or 2 years of relevant experience with a high school diploma or GED.
• Bachelor's degree in scientific, health related or business administration program preferred.
• Experience in clinical trials, familiarity with regulatory requirements, and ability to interact with patients and coordinate care with medical staff.

Responsibilities

• Coordinate data collection and management for assigned protocols.
• Obtain informed consent from participants and coordinate study visits.
• Assist with regulatory documentation and communication with study sponsors.
• Data entry into various database systems and follow-up of patients per protocol.

Skills

Effective communication

Teamwork

Clinical trials

Regulatory knowledge

Patient coordination

Time management

Collaboration

Education

Associate's degree

High school diploma or GED

Bachelor's degree preferred

Job description

Associate Clinical Research Coordinator-Breast page is loaded## Associate Clinical Research Coordinator-Breastremote type: Hybrid (Part -time in Office)locations: Richard M. Schulze Family Foundation Outpatient Centertime type: Full timeposted on: Posted Yesterdayjob requisition id: R-4821### 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.**Summary**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.These 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 skills* Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences* Prior experience in clinical trials is preferred* Familiarity with regulatory requirements in clinical research or ability to successfully learn this* Experience interacting with patients and coordinating care with medical staff* Gain 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 GED+ Bachelor's degree preferred in scientific, health related or business administration program.**Salary Range**$21.65 - $33.05*Salary 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.*## ***If you have the vision, passion, and dedication to contribute to our mission,***## ***then we have a place for you!*****1. Equal Employment Opportunity**Moffitt 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 Accommodation**Federal 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.