Clinical Research Coordinator - Oncology- Denton at Texas Oncology
Denton, TX 76201, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

0.0

Posted On

12 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Addition, Oncology

Industry

Hospital/Health Care

Description

Overview:
Texas Oncology is looking for a hybrid/remote Clinical Research Coordinator to join our team! This position will support the Northeast Texas region. This is a full-time Monday - Friday 8am-5pm position with no weekends, call, or major holidays.
This position can be a level 1, 2 or Sr based on candidate experience
Texas Oncology is the largest community oncology provider in the country and has approximately 600+ providers in 220+ sites across Texas and southeastern Oklahoma. Our 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 nearby. Our 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 breakthroughs. More victories.” ® in their fight against cancer. Today, Texas Oncology treats half of all Texans diagnosed with cancer on an annual basis.

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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 requirements. May 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. May work directly with sponsors. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite.
  • Assists with collection and maintenance of regulatory documents in accordance with USOR SOPs and applicable regulations.
  • May assist in the packing and shipping of lab specimens to central vendors. May be required to complete Hazmat and/or IATA training
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