Oncology Clinical Research Coordinator-RN

About the role

Executes and coordinates the informed consent process for participants in clinical trials and research studies.

Screens potential research participants to determine eligibility for clinical trials and studies.

Provides detailed information about the study, including its purpose, procedures, risks, and benefits, to potential participants.

Ensures that participants fully understand the informed consent document before they sign it, and clarifies any questions or concerns.

Maintains accurate and complete records of the informed consent process, including signed consent forms and documentation of discussions.

Careers in this role involve coordinating or performing biospecimen collection and maintaining HIPAA protected database connecting patient information to biospecimens used in research.

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

Maintains sensitivity to cost containment measures by conserving hospital supplies and human resources while overseeing proposed project budgets.

Conducts research regarding patient screening and clinical eligibility assessments.

Carefully coordinates the care and follow-up of volunteers placed on research studies, trials, and programs.

Provides ongoing support and information to participants throughout the duration of studies.

Works flexible hours and is available for research project-related questions.

Responsibilities

• Performs clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.
• Works independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner.
• Acclimates and integrates into various clinical settings as needed per protocol.
• Administers physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures.
• Communicates effectively with research participants, investigators, research staff and external partners.
• Applies analytical approach to problem solving, obtains and analyzes facts, and applies sound judgement.
• Accepts direction and responds to the changing needs of clinical research units.
• Uses working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill.
• Knowledge of specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment.
• Knowledge of specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials.
• Knowledge of one to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology.
• Bilingual (English/Spanish).

Requirements

• Associate's of Nursing [Required]
• Bachelor's of Nursing [Preferred]
• Field Of Study Nursing Nursing

Qualifications

• Registered Nurse (RN) [Required]
• Basic Life Support - CPR Cert (BLS) [Required]
• Certified Clinical Research Coordinator (CCRC) [Preferred]

Skills

• Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.
• Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner.
• Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures.
• Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research.
• Ability to communicate effectively with research participants, investigators, research staff and external partners.
• Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement.
• Ability to accept direction and respond to the changing needs of clinical research units.
• Working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill.
• 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.
• Bilingual (English/Spanish).

Benefits

Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance

Paid Time Off from Day One

403-B Retirement Plan

Whole Person Well-being Resources

Mental Health Resources and Support

Pet Benefits

Schedule

Full time

Shift Day (United States of America)

Pay

$71,260.80 - $123,215.55