CLINICAL RESEARCH COORDINATOR ASSOCIATE

SPEROS; Magnolia (AR); Hybrid; USD 28,929 - 44,083; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator Associate to support non-therapeutic research protocols, perform data entry, and assist with regulatory documentation. The role involves coordinating study activities, obtaining informed consent, and maintaining study records with moderate supervision.

The position is part of the clinical research team, with responsibilities including data entry, coordination of protocol visits, and communication with sponsors.

Qualifications

• Bachelor's degree in scientific, health related, or business administrative program preferred; Associate's degree required.
• Experience in hands-on research and data entry.
• Knowledge of word processing (Microsoft Office Suite) and database entry.

Responsibilities

• Administers data collection and coordination of clinical trials.
• Obtain informed consent from study participants and collect specimens as needed.
• Enter data into sponsor electronic data capture systems and maintain regulatory documents.
• Assist with miscellaneous study tasks and communicate with study sponsors.

Skills

Microsoft Office

Data entry

Communication

Organization skills

Education

Bachelor's or Associate degree in scientific/health or business admin

Tools

PowerChart EMR

OnCore

sponsor data entry systems

Job description

## CLINICAL RESEARCH COORDINATOR ASSOCIATEApplyremote type: Hybrid (Part -time in Office)locations: Magnolia Hospitaltime type: Full timeposted on: Posted Todayjob requisition id: R-2398### 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**The Clinical Research Coord. Associate (CRC Assoc.) 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.The Clinical Research Coord. Associate (CRC Assoc.) 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 Assoc. recognizes the need for occasional deviation from accepted practice. Requires instructions only on new assignments.## **Requirements:**Education:Bachelor's degree in scientific, health related, or business administrative program preferred; Associate's degree required\*\* In lieu of Associate's degree, high school diploma or GED with two (2) additional years of experience will be consideredExperience:Hands-on research experience preferred with one (1) year in the oncology research setting. Should have knowledge of word processing (Microsoft Office Suite) and database entry. Must have the ability to work well under the pressure of meeting mandatory deadlines. Must have good organizations skills and careful attention to detail. Good oral and written communication skills required. Must have ability to plan, organize and coordinate multiple work assignments. Need to have the ability to read, write, interpret and apply instructions to assigned activities. Successfully demonstrates competency by meeting established competency guideline/check list annually. Preferred: Knowledge of EMR system (ex: Powerchart), clinical trial management systems (ex: OnCore), experience entering data into sponsor electronic data capture systems, general knowledge of medical terminology.**Salary Range**$21.12 - $32.24*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.*Moffitt Career Site## ***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 EEO rights under the law.