Clinical Research Coordinator Sr-Bedford, Tx

US Oncology Network • Bedford, TX

415d

About The Position

The Clinical Research Coordinator at Texas Oncology will support the Bedford, TX location and is responsible for managing and coordinating tasks for multiple clinical research studies. This role involves screening patients for eligibility, ensuring protocol compliance, and participating in patient study visits. The position can be filled at Level 1, 2, or Senior based on the candidate's experience, contributing to the mission of providing high-quality cancer care through research and technology.

Requirements

• Level 1: Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
• Minimum one year of experience in a clinical or scientific related discipline, preferably in oncology required.
• Level 2: Minimum five years of experience in a clinical or scientific related discipline required, preferably in oncology.
• SoCRA or ACRP certification preferred.
• Level Sr: Minimum seven years of experience in a clinical or scientific related discipline required.
• Minimum five years of oncology and/or research experience preferred.
• SoCRA or ACRP strongly preferred.

Nice To Haves

• SoCRA or ACRP certification preferred for Level 1 and 2.
• SoCRA or ACRP strongly preferred for Level Sr.

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.

Benefits

• Medical, Dental, Vision, Life Insurance
• Short-term and Long-term disability coverage
• Generous PTO program
• 401k plan with company match
• Wellness program that rewards healthy lifestyle
• Tuition Reimbursement
• Employee Assistance program
• Discounts on various retailers

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Ambulatory Health Care Services
• Education Level: Associate degree
• Number of Employees: 501-1,000 employees