TI Sr Clinical Research Assistant Clinical Research Coordinator

The Knight Prostate Cancer Research Program is seeking a Therapeutic Interventional (TI) Sr. Clinical Research Assistant (Clinical Research Coordinator) working on complex therapeutic interventional (TI) clinical research protocols and data management.

This TI Sr. Clinical Research Assistant position will be part of the Knight Clinical Research Prostate Programand is responsible for implementation and overall management of oncology clinical trials.

These responsibilities include coordination of all aspects of a study as specifically outlined in the protocol. Primary focus will be subject safety and compliance with the prescribed protocol and Good Clinical Practice. The CRC will work collaboratively with physician nursing and ancillary staff in the scheduling and management of subject research activities. The CRC will maintain accurate complete and timely records on all research subjects including preparation of source documentation and clinical research data/case report forms. . The CRC will have direct patient contact process biological samples and perform other non invasive testing such as ECGs and vitals.

Given the complexities of oncology research and the challenges of working with a terminally ill population strong customer service organizational and interpersonal skills are required. Ability to clearly organize and/or adapt to multiple priorities and deadlines at one time is necessary. Attention to detail service orientation delegation and project management skills and above average critical judgment skills are essential.

Key Responsibilities:

• Study Coordination
• Dissemination of Clinical Research Information to Program
• Institutional Review Board (IRB) Compliance
• Data collection
• Education

Education & experience:

• Bachelors Degree in relevant field AND 1 year of relevant experience OR
• Associates AND 3 years of relevant experience OR
• 4 years of relevant experience OR
• Equivalent combination of training and experience.

Knowledge skills and abilities:

• Ability to prioritize multiple tasks at one time.
• Excellent communication analytical and organizational skills: both written and verbal.
• Ability to work independently and as part of a team while being collaborative in resolving problems.
• Intermediate skills with Microsoft Office (Excel Outlook Access Word and PowerPoint) on Window OS.
• Must have demonstrated excellent customer service skills both on the phone and in person.
• Must possess energy and drive to coordinate multiple projects simultaneously.
• Ability to use tact and diplomacy to maintain effective working relationships

Education & experience:

• Direct clinical research experience
• Research experience with some knowledge of clinical trials
• Experience coordinating different phases of projects including data collection
• Customer service experience
• CCRP or ACRP Certified

Knowledge skills and abilities:

• Microsoft Office Access and/or other networking and database systems
• Medical terminology
• OHSU systems such as Oracle and/or Epic

Apply online. Please be sure to upload a Cover Letter and Resume/CV.

We offer a variety of benefits on top of joining a thriving organization:

• Medical dental and vision coverage at no or low cost to employees
  • Covered 100 for fulltime employees and 88 for dependents
• Several retirement plans to choose from with contributions from OHSU
• 25 days a year of paid time off
• 8 days of sick time off
• Commuter subsidies
• Tuition reimbursement
• Access to group life insurance disability insurance and other supplemental benefits
• Annual Merit Increase
• Growth/Development Opportunities
• Employee discounts to local and major businesses

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