Job details
Job type full-time
Full job description
Overview
Texas oncology is looking for a full-time clinical research coordinator to join our team!this position will support the mary crowley cancer research center in dallasTexas oncology is the largest community oncology provider in the country and has approximately 600+ providers in 220+ sites across texas and southeastern oklahomaOur founders pioneered community-based cancer care because they believed in making the best available cancer care accessible to all communities, allowing people to fight cancer at home with the critical support of family and friends nearbyOur mission is still the same today-at texas oncology, we use leading-edge technology and research to deliver high-quality, high-touch, evidence-based cancer care to help our patients achieve `more breakthroughsMore victories.` ® in their fight against cancerToday, texas oncology treats half of all texans diagnosed with cancer on an annual basis.
All texas oncology employees, except those who work from home full time or who have a medical or religious accommodation, must be fully vaccinated, as defined by the cdc, by december 3, 2021.
Why work for us?
Come join our team that is responsible for helping lead texas oncology in treating more patient diagnosed with cancer than any other provider in texasWe offer our employees a competitive benefits package that includes medical, dental, vision, life insurance, short-term and long-term disability coverage, a generous pto program, a 401k plan that comes with a company match, a wellness program that rewards you practicing a healthy lifestyle, and lots of other great perks such as tuition reimbursement, an employee assistance program and discounts on some of your favorite retailers.
What does the clinical research coordinator do?
The clinical research coordinator is responsible for supporting the management and coordination of tasks for multiple clinical research studies to include screening patients for eligibility and participates in the subject`s study visits and required activities per protocolDuties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers, and participation in required training and education, assures site research quality by practicing in compliance with us oncology research, inc(usor) standard operating procedures (sop), principles of good clinical practice (gcp) and applicable federal, state, and local regulations through osha, cdc and hippaSupports and adheres to us oncology compliance program, to include the code of ethics business standards.
Responsibilities
The essential duties and responsibilities:
Screens potential patients for protocol eligibility.
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials.
Assists with patient care in compliance with protocol requirementsMay disburse investigational drug and maintain investigational drug accountability.
Participates in data collection, entry, and reporting for the subjects.
In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
Participates in required training and education programs as well as monitoring and auditing activities.
Qualifications
The ideal candidate for the clinical research coordinator will have the following background and experience:
Associates degree in a clinical or scientific related discipline required, bachelor`s degree preferred.
Experience in a clinical or scientific related discipline, preferably in oncology preferred.
Experience in microsoft office preferred.
Texas oncology is part of the us oncology network and is an equal opportunity employerAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.
