Study Coordinator

The US Oncology Network • Denver, CO

11h • Onsite

About The Position

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Research Study Coordinator in Denver. Bring your established interventional trials 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 required
• Minimum 3 years research experience on interventional trials
• Requires corrected vision and hearing within normal range.
• All qualified candidates are required to pass a background check and non-federal drug test (which excludes marijuana) post offer of employment and prior to hire.

Nice To Haves

• bachelor's degree preferred

Responsibilities

• Plan the execution and monitor the completion of more intense and complex assigned clinical research protocols.
• Support of other research teams and monitoring adherence to the clinical protocol and preparing reports on the data.
• Work closely with the physician principal investigator, clinical trial sponsor and internal and external study teams for study operation.
• Assists in the execution of highly complex trials for the research team.
• Trials assigned will involve complex protocol management and assisting the data management, clinical and regulatory research teams.
• Assist with the training of new Study Coordinators and Data Coordinators.
• Initiate improvements, tools, processes, and forms to enhance efficiency and quality of work within the research department.
• Planning and tracking of all assigned clinical activity in the lifecycle phases of the startup, interim and close out.
• Updates clinical teams on protocol modifications and specifications including visit schedule, assessment windows, dose modifications, central and local laboratory assessments.
• Creates study specific tools for source documentation as well as checklists and clinic information documents.
• Ensures study specific tools are updated with any amendment(s) or study changes.
• Participates as needed in monitor visits for each assigned trial at each monitoring visit.
• Reviews and comments on follow-up letters.
• Assists with reviews of trial data for responses to queries.
• Provide required study metrics to leadership.
• Assists in physician oversight by updating on protocol issues.
• Assists with sponsor and FDA audit preparation.
• Assists with reviews and responses to monitoring and auditing findings.
• Participates in sponsor meetings as assigned.
• Adhere to professional standards and SOPs established for clinical research.

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: Mid Level
• Education Level: Associate degree