CLINICAL RESEARCH COORDINATOR I - BMT

Moffitt Cancer Center is hiring a Clinical Research Coordinator I to coordinate on-site clinical research activity. The role coordinates patient care and study activities, supports screening and enrollment, monitors protocol compliance, and manages study data, source documentation, and adverse experience reporting.

Responsibilities

The CRC I coordinates clinical research activity on-site at Moffitt Cancer Center

As the primary resource for the protocols, the CRC I will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines with the direction of a mentor or supervisor

The clinical research coordinator I will act as liaison between the investigators, Moffitt regulatory staff and the sponsor

Along with the investigator, the CRC I will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study

In addition, the CRC I is responsible for data and source documentation and adverse experience reporting

The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols

The CRC I is expected to work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures

Preferred

Same as the above with the experience taking place in the oncology setting

Knowledge of EMR system (e.g. Powerchart), clinical trial management systems (e.g. OnCore)

Experience with clinical trials preferred

previous experience in a medically related field or an understanding of medical terminology preferred

Oncology experience

EMR systems

PowerChart

Clinical trial management systems

OnCore

Clinical trial experience

Medical field experience

Medical terminology

Benefits

Hybrid (Part -time in Office)

Company

Comprehensive cancer hospital and research center

Tampa, Florida, USA

http://moffitt.org/

Founded in 1986

10001+ employees

Qualifications

Bachelor's Degree in preferred scientific, health related or business administration program

Bachelors Degree with one (1) year of relevant clinical, health related, scientific, business or research experience

In lieu of a Bachelors Degree, Associates degree with an additional year of relevant experience for a total of two (2) years of experience

CRC I is required to have through knowledge of word processing (Microsoft Office Suite), data base entry, and a basic understanding of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research

Must possess effective verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals

CRC I is required to work under general 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

Must have ability to prioritize and pace one's-self when working under the pressure of deadlines and work volume

Successfully demonstrates competency by meeting established competency guideline/check list annually

Same as the above with the experience taking place in the oncology setting

Knowledge of EMR system (e.g. Powerchart), clinical trial management systems (e.g. OnCore)

Experience with clinical trials preferred

Previous experience in a medically related field or an understanding of medical terminology preferred

Bachelors Degree with one (1) year of relevant clinical, health related, scientific, business or research experience.

In lieu of a Bachelors Degree, Associates degree with an additional year of relevant experience for a total of two (2) years of experience.

Required skills

Clinical Research, Clinical Practice (GCP), Microsoft Office Suite, PowerChart, OnCore, Oncology, Medical Terminology

Preferred skills

Experience with clinical trials preferred

Experience

1+ years