Clinical Research Coordinator I

US Oncology Network • Boulder, CO

254d • $25 - $29

About The Position

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator in Boulder. Bring your established Oncology and or Research experience and join a team dedicated to providing an excellent experience to patients. We realize that it sounds cliché but it is true - taking care of cancer patients is a calling. It's much more than a job. Each of us has a unique story that brought us to Rocky Mountain Cancer Centers (RMCC), but those stories usually share common themes of care, compassion, and commitment. No matter the role each RMCC team member serves in, the goal is the same: to provide the best care possible for each and every one of our patients. Whether we are a nurse holding our patient's hand, or a scheduler on the phone finding an appointment that fits into a patient's schedule, we are deeply connected to our patients and do what we can to help. If this sounds like you, we'd love to have you join our team.

Requirements

• Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
• One year of experience in a clinical or scientific related discipline, preferably in oncology preferred.
• Previous clinical research experience required.
• Experience in Microsoft Office.
• Experience working with physicians preferred.

Nice To Haves

• Excellent communication skills.
• Excellent organizational skills.
• Strong ability to multi-task.
• Excellent time management skills.
• Strong interpersonal skills to interact with multiple people on many different levels.
• High level of attention to detail.
• Ability to work in a fast-paced environment.

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.

Benefits

• Health, dental, and vision plans.
• Wellness program.
• Health savings account.
• Flexible spending accounts.
• Potential for research bonus depending on financials of department after one year of employment.
• 401(k) retirement plan.
• Life insurance.
• Short-term disability insurance.
• Long-term disability insurance.
• Employee Assistance Program.
• PTO.
• Holiday pay.
• Tuition reimbursement.
• Employee paid critical illness and accident insurance.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Ambulatory Health Care Services
• Education Level: Associate degree