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Clinical Research Coordinator

BayCare Health System

Tampa, FLFull-timeSeen 1w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
No compensation found
Location
Tampa, FL
Schedule
Full-time
Work Authorization
Not specified

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Job overview

BayCare Health System seeks a Clinical Research Coordinator at St. Joseph's Hospital to lead and implement clinical trials, ensure protocol adherence, manage regulatory documents, and coordinate patient scheduling and data collection in compliance with GCP, federal, state, and IRB requirements.

Skills & qualifications

RequiredNice to have

Skills

Protocol DevelopmentTrial FeasibilityPatient SchedulingIRB ReportingRegulatory Document MaintenanceInformed Consent ProcessElectronic Data CaptureCase Report Form CompletionAdverse Event ReportingInvestigational Product DispensingMentoring New Team MembersIndependent Work

Qualifications

Bachelor's Degree in Related FieldAssociate Degree in Related FieldHigh School DiplomaTechnical School Degree2 Years Research Experience5 Years Research Experience7 Years Research Experience5 Years LPN Experience1 Year Coordinator RoleCRC CertificationCCRP CertificationCCRC Certification

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
Paid Time Off
Tuition Assistance
401(k) Match

Full job description

Join the team that is revolutionizing health care – BayCare Health System

Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence.

Title: Clinical Research Coordinator

Facility: St. Joseph's Hospital

Responsibilities:

  • Lead and implement clinical trials under the direction of the Principle Investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements.

  • Duties may include:

  • Facilitate protocol development, Complete trial feasibility

  • Ensure study start-up completion worksheet is complete with required protocol specific training of research staff and ancillary departments

  • Ensure adherence to the study protocol and schedule of events, patient visit scheduling for protocol related procedures

  • Screening

  • Study recruitment

  • Preparation of IRB reports

  • Establishment and maintenance of regulatory documents

  • Performing the process of informed consent and HIPPA authorization

  • Clinical follow-up of study subjects including biometric data and specimen collection

  • Creation and completion of source worksheets

  • Building and maintaining EDC systems

  • Collecting source data for electronic data capture (EDC) systems

  • Building and completing Case Report Form (CRF)s

  • Assess patients for trial-related and non-trial related symptoms

  • Reporting of adverse events

  • Serious adverse events

  • Dispensing/accountability of investigational product

  • Participate in additional business activities to recruit new trials or meet recruitment goal

  • Mentors new team members to protocol and site processes

  • Must work independently and use sound judgement while performing job duties

  • Perform duties as assigned under the scope of related certification or licensure

BayCare offers a competitive total reward package including:

  • Benefits (Medical, Dental, Vision)

  • Paid Time Off

  • Tuition Assistance

  • 401K Match and additional yearly contribution

  • Annual performance appraisals and team award bonus

  • Family resources and wellness opportunities

  • Community perks and discounts

BayCare has different levels of Clinical Research Coordinators offering career progression and growth opportunities within the department. The required education/experience/certification for each level is outlined below.

Clinical Research Coordinator II

  • Required - Bachelor's degree in related field in lieu of experience

  • Or - 2 years of research experience with an Associates Degree in related field and CRC (Clinical Research), Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), or CRT/Active NBRC (Respiratory)

  • Or - 5 years of research experience with a High School Diploma and CCRP (Clinical Research) or CCRC (Clinical Research)

  • Or - 5 years LPN experience and 1 year coordinator role with a Technical School and LPN License

  • Or - 2 years LPN and 5 years Research with a Technical School and LPN License

Clinical Research Coordinator III

  • Required - 5 years research experience with an Associates degree in related field and CRC (Clinical Research), Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), or CRT/Active NBRC (Respiratory)

  • Or - 7 years research experience with a Technical School and LPN License

  • Or - 2 years research experience with a Bachelor's degree in a related field

Location: Tampa, FL

Status: Full Time, Exempt: No

Shift Hours: 8:00AM - 4:30PM

Weekend Work: None

Equal Opportunity Employer Veterans/Disabled

Position Clinical Research Coordinator

Location Tampa:St Josephs | Clinical | Full Time

Req ID 174339

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