Providence is calling a Supervisor Clinical Research - Program Development, Neuro Muscular Skeletal (1.0 FTE, Days) to St Vincent Mob East Pavillion in Portland, OR. Monday-Friday schedule with flexible start times between 7am to 9 am.
$1,000 sign-on bonus for eligible external hires that meet required qualifications and conditions for payment.
Apply today! Applicants that meet qualifications will receive a text message with some additional questions from our Modern Hire system.
We are seeking a Supervisor Clinical Research - Program Development Neuro Muscular Skeletal. The Clinical Research Supervisor will function under the direction of the Clinical Research Manager, overseeing diverse activities related to clinical studies. Responsibilities include managing trial assignment with attention to detail, efficiency and accuracy, providing leadership and day-to-day supervision of the Clinical Trials Coordinators, Sr. Clinical Research Assistants, and Clinical Research Assistants in the research program(s), communicating with Regional Research to ensure timely resolution or completion of regulatory/contract issues, and maintaining effective communication with investigators, sponsors, and ancillary departments that support PBSI studies regarding study progress, assisting with the development of departmental policies, procedures, and systems for conducting clinical trials, and mentoring and training new staff.
In this position you will have the following responsibilities:
Responsible for day-to-day supervision of Clinical Trials Coordinators and Clinical Research Assistants and related Human Resource issues.
Responsible for all aspect of clinical trial management, including coordinating study visits, completing assessments and procedures according to protocol, collecting source documents, completing case reports forms, tracking/reporting serious adverse events and protocol deviations, and entering data into clinical trial databases, and resolving queries as necessary.
Assist investigator and manager to review protocol, assess feasibility, and allocate resources and services needed to initiate new study.
Work closely with sponsors and clinical research organizations to coordinate site selection, site initiation, other study startup activities, and monitoring and close out visits.
Work closely with Regional Research in the completion of regulatory/IRB submission and study budget/agreement for new studies.
Attend investigators meetings and other study related training and meetings.
Monitor study progress and keep manager appraised of issues requiring action to ensure study objective and timeline are met.
Serves as a resource liaison for investigators and other researchers involved in the day to day management of patients on clinical trials and provide back up support in the absence of other research staff.
Implements quality assurance principles for the controls for accuracy, completeness, and confidentiality of research data.
Provides support to individual physician investigators to ensure compliance with treatment plans and follow-up studies, and assesses outcomes. Conducts follow-up for assessment of off-treatment patients.
Establishes positive working relationships within the department, throughout the hospital and between other institutions to promote research collaboration.
Performs other duties as requested.
Required qualifications for this position include:
Bachelor's Degree in a scientific -OR- health services discipline
Society of Clinical Research Associates (SOCRA) -OR- Association of Clinical Research Professionals (ACRP) certification
Five (5) years clinical research professional experience
Experience training, mentoring, and developing staff
Strong experience with monitoring audit facilitation; demonstrated effectiveness in resolving issues of varying complexity in a professional manner
Experience with medical terminology
Advanced level proficiency in Microsoft Access, Excel, Word, Internet Explorer, and Outlook
Preferred qualifications for this position includes:
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Job Category: Non-Clinical Lead/Supervisor/Manager
Req ID: 347979