Clinical Research Coordinator I Oncology

Texas Health Huguley FWS; Orlando (FL); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading healthcare organization seeks a Clinical Research Coordinator I for its Oncology department. In this role, you will manage patient interactions, oversee recruitment for clinical trials, and ensure compliance with regulatory guidelines. This position offers the opportunity to impact research positively while working within a prestigious hospital environment.

Benefits

Benefits from Day One

Paid Days Off from Day One

Mental Health Resources and Support

Pet Insurance

Qualifications

• FDA compliance and regulatory knowledge essential.
• Experience in human life sciences/biomedical research is preferred.

Responsibilities

• Coordinate patient recruitment and consent for clinical trials.
• Conduct data collection and maintain compliance with study protocols.
• Collaborate with various departments to ensure research standards.

Skills

Patient screening

Data collection

Biospecimen collection

Education

Bachelor’s degree in Healthcare or related field

Associates degree in Healthcare and two years of clinical research

Graduate of an accredited allied health certificate program

Job description

Job Description - Clinical Research Coordinator I Oncology (25019029)

Job Description

Clinical Research Coordinator I Oncology (

Job Number:

25019029 )

Description

Clinical Research Coordinator I- AdventHealth Orlando

All the benefits and perks you need for you and your family:

- Benefits from Day One

- Paid Days Off from Day One

- Mental Health Resources and Support

- Pet Insurance*

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full Time

Shift : Days

The community you’ll be caring for: AdventHealth Orlando

• Located on a lush tropical campus, our flagship hospital, 1,368-bed AdventHealth Orlando
• Serves as the major tertiary facility for much of the Southeast, the Caribbean and South America
• AdventHealth Orlando houses one of the largest Emergency Departments and largest cardiac catheterization labs in the country
• We are already one of the busiest hospitals in the nation, providing service excellence to more than 32,000 inpatients and 125,000 outpatients each year

The role you’ll contribute:

The Clinical Research Coordinator I (CRC I) is involved in all aspects of research conducted including patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs. Specific activities to include: Research participant recruitment and consenting for the therapeutic areas they serve, provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies, and the coordination of biospecimen collection (i.e. blood, tissue) through collaborative interaction with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance.

The value you’ll bring to the team:

•Execute and coordinate the informed consent process for AdventHealth Research Institute participants in clinical trials and research studies across multiple locations.This may require travel between sites and research laboratories, and/or the use of technology.

•Responsible for all aspects of research conducted including patient screening, assessing eligibility, and coordinating the participation and follow-up of volunteers placed on research studies, trials, and programs.

•Coordinate research participant recruitment and consenting for the therapeutic areas they serve

•Provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies

•Coordinate or perform biospecimen collection (i.e. blood, tissue) and maintain HIPAA protected database connecting patient information to biospecimens used in research; perform patient chart review and data collection.

•Collaborative interaction with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices, to ensure ongoing regulatory and protocol compliance.

•Through collaboration with assistant clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems.

•Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents.

•Serves as the study-specific point of contact for participants, investigators, research staff, hospital departments and external research partners.

•Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the Institutes research division intended to meet standards. Ensures all patient-facing activities are compliant with clinical research standards and AHRI procedures.

•Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.

Qualifications

The expertise and experiences you’ll need to succeed :

• Bachelor’s degree in Healthcare or related field with no research experience OR Bachelor’s degree in any field with research experience.
• Associates degree in Healthcare or related field and two (2) years of clinical research or healthcare experience or
• Graduate of an accredited allied health certificate program with four (4) years of clinical research or healthcare experience.
• Preferred qualifications:
  • Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment
  • Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials.
  • One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology

o Master’s degree in Healthcare, Research, or related field

o Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA))

o American Heart Association Basic Life Support (BLS)

o Other certification as applicable to clinical degree or program (i.e. medical assistant, medical technician, phlebotomy)