Clinical Research Coordinator I- Plano West

The US Oncology Network•Plano, TX

1d•Onsite

About The Position

Texas Oncology is seeking a Clinical Research Coordinator to support the Plano West location in the Oncology Clinical Research department. This position offers typical hours of Monday-Friday from 8:30 am to 5:00 pm. The level of this position (I, 2, or Sr) will be determined by the candidate's experience. Texas Oncology is the largest community oncology provider in the country, committed to making advanced cancer care accessible in local communities. Our mission is to deliver high-quality, high-touch, evidence-based cancer care using leading-edge technology and research, enabling patients to achieve 'More breakthroughs. More victories.' in their cancer fight.

Requirements

Associate's degree in a clinical or scientific related discipline required.
Minimum one year of experience in a clinical or scientific related discipline, preferably in oncology required.
Minimum five years of experience in a clinical or scientific related discipline required, preferably in oncology.
Minimum seven years of experience in a clinical or scientific related discipline required.
Minimum five years of oncology and/or research experience preferred.

Nice To Haves

Bachelor's degree preferred.
SoCRA or ACRP certification preferred.
SoCRA or ACRP strongly preferred.

Responsibilities

Screens potential patients for protocol eligibility.
Presents trial concepts and details to 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.