Clinical Research Coordinator II - Oncology

BayCare Health System; Clearwater (FL); On-site; USD 55,000 - 75,000; Full time

Job summary

BayCare Health System is seeking a Clinical Research Coordinator II to conduct and manage clinical research studies in Clearwater, FL. Responsibilities include coordinating study protocols, patient assessments, and regulatory compliance. The ideal candidate will have a degree in a related field and relevant research experience, offering a chance to contribute to innovative healthcare solutions.

Benefits

Paid Time Off

Tuition Assistance

401K Match

Annual performance appraisals

Family resources and wellness opportunities

Community perks and discounts

Qualifications

• Bachelor's Degree in related field or equivalent experience.
• 2 years of research experience or CRC license.
• 5 years of research experience with High School diploma or GED.

Responsibilities

• Coordinate and implement clinical research studies under supervision.
• Ensure adherence to study protocols and manage patient schedules.
• Prepare IRB reports and manage regulatory documents.

Skills

Clinical research

Patient assessment

Regulatory compliance

Data collection

Education

Bachelor's Degree in related field

Associates Degree plus CRC certification

High School Diploma/GED with CCRP or CCRC

Technical School LPN with relevant experience

Job description

Clinical Research Coordinator II - Oncology

Clinical Research Coordinator II - Oncology

Direct message the job poster from BayCare Health System

Talent Acquisition Senior Recruiter at BayCare Health System

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 II - Oncology

This position can be filled at a Clinical Research Coordinator I, II, or III level based on experience, education, and certification. Speak with a recruiter today for more information on our career ladder!

Responsibilities:

• Coordinate and implement clinical research studies under the direction of the Principal Investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements.
• Duties may include:
• 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, Creation and completion of source worksheets.
• Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion.
• Assesses patients for trial-related and non-trial related symptoms, reporting of adverse events, serious adverse events, and dispensing / accountability of investigational product.
• Must work independently and use sound judgment while performing job duties.
• Perform other duties as assigned under the scope of related certification or licensure.

BayCare offers a competitive total reward package including:

• 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

Required Education, Experience, and Certifications:

• Bachelor's Degree in related field in lieu of experience and certifications
• Associates Degree in related field and CRC (Clinical Research) Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), CRT/Active NBRC (Respiratory); with 2 years of Research Experience
• High School Diploma/GED and CCRP (Clinical Research) or CCRC (Clinical Research) with 5 years research experience
• Technical School Licensed Practical Nurse and LPM License with 5 years LPN experience and 1 year coordinator level role or 2 years LPN experience with 5 years research experience

Location: Clearwater, FL

Status: Full Time, Exempt: No

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

Equal Opportunity Employer Veterans/Disabled

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Hospitals and Health Care

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