Clinical Research Coordinator C (Department of Neurosurgery)
Clinical Research Coordinator C (Department of Neurosurgery)
University Overview
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The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
Posted Job Title
Clinical Research Coordinator C (Department of Neurosurgery)
Job Profile Title
Clinical Research Coordinator C
Job Description Summary
This position will be a resource for best practices of managing major clinical trials. The coordinator will provide guidance to both study trials and device trials. The incumbent will be a liaison to departmental interaction such as the investigational team, the nursing units and sponsor. They will be a resource to other members of the team and will oversee the implementation of new clinical trials. Will review all new trials to help identify the challenges and opportunities discovered. Will problem-solve the challenges to implement a plan of action. Work with the regulatory manager to ensure that submissions to the IRB are completed in a timely manner.
Job Description
Job Responsibilities
- Coordinate Phase I-IV clinical trials
- Recruit, consent and screen patients according to protocol
- Schedule patient visits and any necessary testing. Monitor patients per protocol requirements and ensure adherence to protocol requirements
- Organize and maintain all required documentation- including source documentation, case report forms, and research charts. Collect, review and report study data, Complete case report forms and resolve data queries
- Process and ship study specimens including blood, urine and tissue samples
- Participate in the initiation, monitoring, audit, and close-out visits. Participate in study team meetings disease site group meetings, and ongoing protocol training/compliance meetings
- Develop/maintain study specific case report forms and source document tools
- Participate in the coordination of Phase I-IV clinical trials (10% Essential: 1),Prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all other applicable review
- Other duties and responsibilities as assigned
Qualifications
- Bachelor of Science and 4 to 6 years of experience or equivalent combination of education and experience is required.
Position contingent upon funding.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$62,000.00 - $66,567.80 Annual Rate
Equal Opportunity Statement
The University of Pennsylvania is an equal opportunity employer. Candidates are considered for employment without regard to race, color, sex, sexual orientation, religion, creed, national origin (including shared ancestry or ethnic characteristics), citizenship status, age, disability, veteran status or any class protected under applicable federal, state or local law.
Special Requirements
Background checks may be required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
University Benefits
- Health, Life, and Flexible Spending Accounts: ...
- Tuition: ...
- Retirement: ...
- Time Away from Work: ...
- Long-Term Care Insurance: ...
- Wellness and Work-life Resources: ...
- Professional and Personal Development: ...
- University Resources: ...
- Discounts and Special Services: ...
- Flexible Work Hours: ...
- Penn Home Ownership Services: ...
- Adoption Assistance: ...
To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay
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