Clinical Research Project Manager - Supervisor

Apply for Job Job ID 365408
Location Twin Cities
Job Family Research-Support
Full/Part Time Full-Time
Regular/Temporary Regular
Job Code 7352P4
Employee Class Civil Service
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About the Job

In close partnership with the Clinical Research Director, this position is responsible for the research operations of a portfolio of research studies and a team of research staff. Research Project Managers are working managers, and duties include: assisting with the development of research studies, securing regulatory approvals, facilitating budget development and financial management, monitoring study accrual, and ensuring successful overall study coordination and compliance with applicable regulations and guidelines.

Major Duties/

Clinical Trial Portfolio Management and Oversight (30%)

• Facilitate efficient and effective study start-up, which includes:
  • Determining billing designations, informing calendar build, ensuring accurate pricing and budget development; partner with CTFS for budget development and negotiation for industry-sponsored trials; partner with PedsRSS for grants and subawards
  • Ensuring IRB and other regulatory approvals; partner with Regulatory Specialists for effective and efficient regulatory process and complete documents
  • Collaborate with clinical partners to establish study logistics, including specimen collection and management, investigational product management, clinical procedures, etc.
  • Serve as point person for faculty investigators and research sponsors; build effective relationships that promote research ethics and high quality research in children
  • Facilitating effective project planning and start-up for investigator-initiated research following federal regulations and local policies.
• Ensure compliance with University requirements for registering research projects, obtaining ancillary reviews, and updating study records in the Clinical Trials Management System.
• Utilize extensive knowledge and comprehension of Code of Federal Regulations (CFR), Good Clinical Practice (GCP) guidelines, and National Institute of Health (NIH) research rules to oversee all aspects of study conduct, including:
  • Participant recruitment and accrual monitoring
  • Compliant regulatory management, including continuing reviews and amendments
  • Directing staff roles and responsibilities per Delegation of Authority
  • Protecting the safety and health of human subjects

Clinical Research Coordination (40%)

• Be primary contact and information resource to University faculty and staff for protocol specific queries, including availability of trials, enrollment requirements, specimens needed, etc.
• Engage with investigators and ensure research procedures comply with regulations, policies, and best practices.
• Screen and recruit potential research subjects.
• Work with investigators to ensure subject eligibility, facilitate subject enrollments, ensure the appropriate recording of adverse events, and timely acquisition of research tissue.
• Coordinate subject visits, ensure protocol requirements are met
• Ensure timely and accurate data submission; engage with providers and investigators to ensure adequate source documentation is available; accurate interpretation and recording of data; maintenance of subject research charts.
• Facilitate the timely review and reporting of adverse reactions and severe adverse events
• Ensure compliance with requirements for registering subjects and study visits; facilitate compliant research billing of services
• Contribute to the production of research publications or presentations of research data

Research Operations and Process Improvement (10%)

• Serve as the primary CRP Education resource for the clinical research program and pediatric research teams, including implementation of new processes and standards
• Participate in work on internal business issues of moderate complexity, and recommend solutions and best practices
• Support development of standardized research practices and workflows
• Attend professional development and training sessions to ensure compliance with newest policies and procedures.
• Monitor trends and offer suggestions for improvements
• Assist with quality monitoring according to departmental procedures
• Support other special projects and program initiatives as directed

Staff Development and Supervision (20%)

• Direct supervision and mentoring of research support staff
• Interview, hire, and train new team members
• Perform performance evaluations and promote professional development
• Participate in the training of additional staff as requested

Salary Range: $78,000-$88,000/yr

All required qualifications must be included in the application materials

Required Qualifications:

• BA/BS in a related field, and five years of relevant experience; or advanced degree with three years of relevant experience; or a combination of related education and experience to total nine years
• Experience preparing and managing IRB and other regulatory review submissions, including securing initial IRB approvals and required per-review approvals.
• Experience in Clinical Research

Preferred Qualifications:

• Expert knowledge of the federal regulations governing human subject research, including protections for vulnerable populations
• Computer proficiency, and ability to navigate multiple software applications.
• Electronic document management experience and strong skills with Adobe and Microsoft Word
• Detail-oriented with exceptional organizational, planning and problem-solving skills
• Ability to work independently, as a part of a team and with changing priorities
• Demonstrated ability to maintain deadlines and prioritize assignments
• Excellent written, verbal and interpersonal skills
• Masters-level degree in relevant field
• Project management experience
• Clinical Research Certification (CCRC or CCRP)

Essential Employees:

The successful candidate will be designated as an Essential Employee. Essential Employees are expected to report to campus during a University State of Emergency (reduced operations or campus closure) unless specifically directed by the Department not to report or if directed by civil emergency or medical authorities not to report for health and safety reasons. As an Essential Employee, you must report to campus even if the closure is less than 3 days.

At University of Minnesota Department of Pediatrics, our experts, care teams and researchers are illuminating cures that save young lives. Our ground-breaking treatments are improving the lives of children who are ill or injured, and are becoming the standards of care for children across the country and around the world.

The Pediatric Clinical Research Services program serves the University's research mission by providing comprehensive research support to faculty investigators conducting medica.