Columbus , Nebraska
Boise, Idaho
Nashville, Tennessee
Saint Louis, Missouri
Posted: 21-Nov-23
Location: Dallas, Texas
Salary: Open
Categories:
Internal Number: 23021292
Shift: 8AM-5PM
Location: In Office at 909 N Washington Ave, Dallas, 75246
JOB SUMMARY
The clinical research supervisor position will support the research department at Baylor Scott & White Institute for Rehabilitation. Our current research efforts center around studying traumatic brain injury, using robotics during inpatient and outpatient spinal cord rehabilitation, stroke recovery, and supporting a healthy lifestyle for outpatients living in the community. With a diverse patient group from acute care therapy, inpatient rehabilitation, and outpatient therapy we are able to create unique research opportunities for our patients. In this position you will be part of a team including PhD investigators, Physical Medicine and Rehab (PM&R) physicians, project managers, post doctorate fellows, physical therapists, and clinical research staff. The majority of research projects include Investigator initiated research that is funded by federal and foundation grants.
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
- PhD Preferred
- EXPERIENCE - 2 Years of Experience