Senior Professional Research Assistant
- Employer
- University of Colorado Anschutz Medical Campus
- Location
- Denver, CO
View more
- Administrative Jobs
- Academic Affairs, Research Staff & Technicians
- Employment Type
- Full Time
- Institution Type
- Four-Year Institution
You need to sign in or create an account to save a job.
Description
Qualifications
Minimum Requirements
Job Category: Faculty
Primary Location: Aurora
Schedule: Full-time
Posting Date: Jan 13, 2022
Unposting Date: Ongoing
University of Colorado – School of Medicine
Senior Professional Research Assistant
The University of Colorado has a requirement for COVID-19 vaccinations and full completion thereof by 9/1/21 or upon start date. Information regarding this requirement, and exemptions can be found at: Anschutz: https://www.ucdenver.edu/docs/librariesprovider284/default-document-library/3000-general-admission/3012---covid-19-vaccination-requirement-and-compliance.pdf?sfvrsn=4e9df3ba_2 Denver: https://www.ucdenver.edu/coronavirus Exemptions vary by campus location/department. Campus/Unit-Specific Exemptions:
- Anschutz Campus – Exemptions are allowed for medical or religious reasons.Denver Campus - Exemptions are allowed for medical, religious, or personal reasons.Consolidated/Central Services Administration – Will follow Anschutz policy on exemptions.
The University of Colorado Denver seeks individuals with demonstrated commitment to creating an inclusive learning and working environment. We value the ability to engage effectively with students, faculty and staff of diverse backgrounds
The University of Colorado division of Gynecologic Oncology is looking to hire a full time Clinical Research Supervisor. This position oversees clinical studies performed at the CU Cancer Center and directly supervises the clinical research staff. The role will be to coordinate the daily activities required to conduct clinical research protocols, recruitment and enrollment of research participants, schedule study participant clinic visits, accurately record and enter data, process biospecimens, respond to data queries from study sponsors, and support physician investigators. Additionally, the supervisor will assist in regulatory compliance and submissions for all clinical trials. The position may be utilized to support research at the main Anschutz Medical Campus as well as in Northern Colorado. The supervisor in this position will not be called on to make independent medical decisions at any time, but a solid fundamental knowledge of biological and medical sciences is necessary for this position. Additionally, an appreciation of accepted methods of clinical research is highly desirable. Professional FieldMedical/Clinical Research Supervision Received Division of Gynecologic Oncology investigators and administrative director. Discussions with the research team and Director of clinical research will be held on a regular basis. Supervision ExercisedThis individual is responsible for the supervision, discipline, and evaluation of all members with her/his designated clinical research team(s). Examples of Work Performed- Arranges orientation and provides training, supervision and leadership to the clinical research staff. Assists clinical research staff with technical issues, problem solving and intervention when appropriate; delegates responsibility for elements of the conduct of selected clinical trials. Acts as an interdepartmental liaison with UCH clinic staff (i.e. investigators, nurses, clinic support staff, laboratory, pharmacy, radiology). Plans and directs investigator and coordinator meetings including but not limited to pre-study qualification visits, initial orientations, study audits, and closeout visits. Makes recommendations regarding clinical research personnel issues, including performance evaluations, counseling, and disciplinary actions with guidance from the Director of Clinical Research.Work with finance team members to resolve discrepancies and to review account balances on a regular basis.Participate in external audits and internal process improvement strategies to promote consistent best practices.Assures compliance with all protocol details which includes ensuring the capture of all data points requested on a protocol-specific basis and ensuring that tests and procedures required by clinical protocols are performed and documentedActs as support and able to fill in for team PRA/CRC role when necessary.Assists with regulatory compliance and submissions
Qualifications
Minimum Requirements
- Master’s degree or equivalent experience as determined by the Dean or his or her designeeProficient with Microsoft Office including Outlook, Excel, Word and PowerPoint.Experience working in a healthcare setting2 years of clinical research experience
- CCRC – Certified Clinical Research CoordinatorCCRP – Certified Clinical Research ProfessionalCCRA – Certified Clinical Research Associate
- Four (4) years of clinical and/or clinical research experience. One year of oncology researchPersonnel management experienceExperience serving as a primary coordinator for clinical trialsExperience teaching, orienting and mentoring new employees to clinical researchExperience assisting in the development of policy, procedure or patient education materials related to clinical research
Job Category: Faculty
Primary Location: Aurora
Schedule: Full-time
Posting Date: Jan 13, 2022
Unposting Date: Ongoing
You need to sign in or create an account to save a job.
Get job alerts
Create a job alert and receive personalized job recommendations straight to your inbox.
Create alert