Posted in Other 14 days ago.
The SMMART TI Senior Clinical Research Assistant (Clinical Research Coordinator) will be responsible for the overall patient management of SMMART-operated clinical trials, and/or in conjunction with Knight Disease Teams that directly partner with our program on SMMART-collaborative clinical trials. This includes but is not limited to development and upkeep of research study forms and CRC training materials to perform study-related activities, verification of patient eligibility for study participation, consenting patients to participate and triaging patient questions when appropriate, maintaining adequate source documentation and data entry for proper conduct of protocol in accordance with applicable NCI and FDA guidelines, and maintenance of participant records and study files. This position will be responsible for placing study-related research orders in EPIC, monitoring study drug compliance with the clinical team, and collection and procurement of biological specimens (such as tissue and blood) when necessary. Involvement of other non-invasive testing, such as ECGs, may occasionally occur as needed. This position may also assist management with verification that appropriate research activities were performed for the appropriate participant(s) and clinical trial(s). This position will have direct and frequent patient contact both in-person and via phone/virtual.
Level of research responsibility for this position requires general supervision. This position will be expected to complete responsibilities with moderate oversight to perform tasks, and requires increased innovation and problem solving, understanding of complex protocol requirements and adherence, and participant data management. This position may also be asked to assist management with other administrative projects or duties as needed.
The TI Sr. Clinical Research Assistant (Clinical Research Coordinator) may also assist in the continuing education and compliance of key stakeholders (physicians, residents, interns, nurses, and other related personnel) for compliance to and knowledge of SMMART clinical trials, workflows, and study activities. This position always promotes the mission of the Knight Cancer Institute through our professional standards of customer service, reliability, productivity, professionalism, accuracy, timeliness, and problem-solving.
Key Responsibilities include:
Education and experience:
Bachelor's degree in relevant field AND 1 year of relevant experience OR
Associate’s degree AND 3 years of relevant experience OR
4 years of relevant experience OR
Equivalent combination of training and experience.
Required Competencies:
PI241033057
Siemens Medical Solutions USA, Inc. |
Equipment Depot |
Portland State University |