CLINICAL RESEARCH COORDINATOR I

at  H Lee Moffitt Cancer Center

Tampa, FL 33612, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate31 Oct, 2024Not Specified07 Aug, 20242 year(s) or aboveCredentialsNoNo
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Description:

The Rad Onc Data Management department in the Clinical Trials Office is looking for a Clinical Research Coordinator I.

Position Highlights:

  • Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor.
  • Act as liaison between the investigators, Moffitt regulatory staff and the sponsor.
  • Will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
  • Responsible for data and source documentation and adverse experience reporting.
  • Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
  • Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.

Credentials and Qualifications:

  • Bachelor’s degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience
  • In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience
  • CCRP/CCRC or equivalent preferred.

Location: H. Lee Moffitt Cancer Center & Research Institute · Rad Onc Data Mgmt
Schedule: Full Time, Day Shift, 8-

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Business Administration, Administration, Business

Proficient

1

Tampa, FL 33612, USA