Saint Louis, Missouri
Morrisville, North Carolina
Raleigh, North Carolina
Gainesville, Georgia
Posted: 14-Aug-24
Location: Dallas, Texas
Salary: Open
Categories:
Internal Number: 24011209
Clinical Research Supervisor - Flow Cytometry
JOB SUMMARY
Provides day-to-day supervision of flow core based research and staff. The ideal candidate will have an in-depth understanding and hands-on experience in flow cytometry sample processing, specimen analysis and cell sorting under BSL2+ conditions, with strong leadership and communication skills. This individual will be an integral part of our project development process by contributing scientific expertise, experimental support and solutions for our customers in order to help drive science forward. The supervisor will collaborate with research staff internal and external to the lab. The Clinical Research Supervisor provides day-to-day supervision of department based Clinical Research staff. This position develops, negotiates and monitors budgets related to funded research projects, facilitates the implementation of clinical research projects, and monitors for quality and timely completion.
ESSENTIAL FUNCTIONS OF THE ROLE
- Writes and assists in the development of proposals, grants, contracts and budgets for the department.
- Assists in the development of new protocols and other materials provided by study sponsors and provides input to Principal Investigators (PI) and management regarding clinical and research issues in order to establish financial and clinical feasibility.
- Assists various PIs, through delegated authority, in conducting clinical trials per federal, state and institutional guidelines.
- Prepares initial submission of projects, notification of amendments, Serious Adverse Event (SAE) reports, continuing review reports and other reports submitted to the Institutional Review Board (IRB). Reviews submissions prepared by staff to ensure that all submissions meet established standards.
- Oversees case report form completion performed by staff for all studies and assists in the coordination of audits by the study sponsor monitors. Monitors assigned Clinical Research funds.
- Orientates, trains, supervises and evaluates Clinical Research staff. Encourages continuing growth through more complex responsibilities and formal education programs. Coordinates project assignments for staff.
- Establishes and maintains good relations with the public, patients and staff; promotes department's research programs.
- Monitors communication with the IRB, Food and Drug Administration (FDA) and other applicable regulatory agencies.
KEY SUCCESS FACTORS
- Research certification or other certifications per specialty area preferred.
- Basic Life Support (BLS) per department requirements.
- Proven written and oral communication skills.
- Proven computer skills, including Microsoft office, Excel and PowerPoint.
- Ability to manage time impressible projects in order to meet deadlines.
- Ability to establish and maintain effective working relationships.
- Excellent leadership skills.
BENEFITS
Our competitive benefits package includes the following.
- Immediate eligibility for health and welfare benefits
- 401(k) savings plan with dollar-for-dollar match up to 5%
- Tuition Reimbursement
- PTO accrual beginning Day 1
Note: Benefits may vary based upon position type and/or level
QUALIFICATIONS
- EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification
- EXPERIENCE - 2 Years of Experience
- A bachelor's degree in biology or a closely related discipline is required. Minimum 5 years hands-on experience with flow cytometry (minimum of 5 colors) including design, acquisition, and analysis. Experience with multi-parameter sorting preferentially on BD flow cytometers (AriaII and Influx) is preferred. Thorough and demonstrated understanding of commercial flow cytometry software including Flow Jo and BD FACS Diva. Knowledge in multi-parameter flow cytometry analysis of immune cells, especially utilizing large antibody panelsStrong background in immunology and/or microbiology.