Clinical Research Coordinator- Clinical Research and Sponsored Programs
Saint Francis Health SystemOur take on this role
About this role
Coordinate clinical trials through patient recruitment, informed consent, data collection, and adverse event reporting. The full-time schedule is Monday–Friday, 8:00am–5:00pm, and the role requires at least two years of related clinical research experience.
What could you bring from clinical work?
- Nurses: Your experience recognizing and documenting adverse events could help with timely, accurate study safety reporting.
- OTs and SLPs: Explaining assessments and educating patients about participation may help you explain study requirements and obtain informed consent.
- PTs: Collecting outcome measures and interpreting clinical records could help you collect and analyze research data.
- Social workers: If you've coordinated communication among patients, families, and clinicians, that experience could help you serve as their research contact for information and issue resolution.
Full job description from Saint Francis Health System
Current Saint Francis Employees - Please click HERE to login and apply.
Full Time
Days
Monday - Friday | 8:00am - 5:00pm
The ideal candidate would demonstrate strong verbal and written communication skills. They should have a working knowledge of the Epic Research Module or a willingness to learn. High attention to detail and accuracy in data entry and documentation are essential, as is the ability to manage multiple projects/studies simultaneously through effective time management. The candidate must be able to work independently as well as collaboratively within a multidisciplinary research team, exhibit adaptability to support cross-coverage and evolving departmental needs, maintain professional conduct and confidentiality, and show initiative in learning and problem-solving within their scope of responsibilities.
Job Summary: The Clinical Research Coordinator performs clinical research activities, investigations, and develops and compiles reports based on records, observations, test results and other information received for the purpose of advancing knowledge through clinical trial research in multiple disciplines. This role ensures timely and accurate reporting of adverse events, and helps maintain study budgets, supplies, and regulatory documentation.
Minimum Education: Bachelor’s degree, preferred.
Licensure, Registration and/or Certification: Certified Clinical Research Professional (CCRP), preferred.
Work Experience: Minimum 2 years of related experience in clinical research with a medical or scientific background.
Knowledge, Skills and Abilities: Comprehensive knowledge of medical terminology and current healthcare management methodology. Ability to use logical and/or scientific thinking to solve problems. Ability to follow and interpret written and verbal instructions. Ability to perform basic algebraic and geometric calculations as needed to computer dosage levels of drugs based on lab test results. Working knowledge of clinical research practices and protocols. Working knowledge of applicable guidelines and laws pursuant to clinical research. Ability to work in Word proficiently with working knowledge of Excel and Access or other database program used in the production of reports. Effective interpersonal, written, and verbal communication skills. Ability to organize and prioritize work in an effective and efficient manner. Ability to be detail oriented as required in the examination of clinical and numerical data.
Essential Functions and Responsibilities: Recruits and screens clinical research patients for protocol eligibility. Obtains informed consent through patient education; instructs patients regarding study design and purpose, anticipated side effects, patient's responsibilities and rights. Serves as a resource to physicians concerning protocol requirements and determines data requirements as delineated by each trial. Performs data collection and analysis of test results and records relating to clinical research. Collects appropriate data from physician offices and patient charts regarding research studies. Serves as liaison for patients, patient families, physicians, and regulatory body representatives for the purpose of providing a single point of contact for information, education and issue resolution. Coordinates with physician offices or treatment sites to assure billing compliance and drug accountability. Instructs the research data analyst to ensure that protocol parameters and treatment guidelines are correctly applied. Prepares new study applications, writes informed consent and submits for Institutional Research Ethics Board (IREB) approval according to applicable regulations.
Decision Making: Independent judgment in making decisions involving non-routine problems under general supervision.
Working Relationships: Coordinates activities of others (does not supervise). Leads others in same work performed (does not supervise). Works directly with patients and/or customers. Works with internal and/or external customers via telephone or face to face interaction. Works with other healthcare professionals and staff. Works frequently with individuals at Director level or above.
Special Job Dimensions: None.
Supplemental Information: This document generally describes the essential functions of the job and the physical demands required to perform the job. This compilation of essential functions and physical demands is not all inclusive nor does it prohibit the assignment of additional duties.
Clinical Research and Sponsored Programs - Yale Campus
Location:
Tulsa, Oklahoma 74136