Job Description

One of the largest and most comprehensive providers of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator in Boulder.

We realize that it sounds cliché but it is true - taking care of cancer patients is a calling.

No matter the role each 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.

Pay is based on several factors including but not limited to education, work experience, certification, etc.

A wide salary range is posted for this position and any job offer is based upon a salary analysis to comply with the Colorado Equal Pay for Equal Work Act. The salary analysis considers relevant experience, education, and certifications as compared to others doing substantially similar work. While all offers are compliant with the Colorado Equal Pay for Equal Work Act, there is no guarantee an offer will be at the top of the posted range based on the salary analysis.

As of the date of this posting, in addition to your salary, we offers the following benefits for this position, subject to eligibility requirements: 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, and employee paid critical illness and accident insurance.

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.

Skills/Qualifications:

• 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.

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