
Supv Clinical Research
Dallas, TXJobSeen 2w agoSeen in employer's feed 2 days ago
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The Clinical Research Supervisor oversees daily supervision of Clinical Research staff and develops, negotiates, and monitors budgets for funded research projects. The role facilitates clinical research project implementation and timely completion, supports protocol and submission development, and monitors regulatory communications. It also coordinates staff assignments, training, and evaluation. Research certification or specialty-area certifications are preferred; Basic Life Support is required per department requirements.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
About Us
Here at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and White is the largest not-for-profit healthcare system in Texas that empowers you to live well.
Our Core Values are:
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We serve faithfully by doing what's right with a joyful heart.
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We never settle by constantly striving for better.
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We are in it together by supporting one another and those we serve.
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We make an impact by taking initiative and delivering exceptional experience.
Benefits
Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include:
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Immediate eligibility for health and welfare benefits
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401(k) savings plan with dollar-for-dollar match up to 5%
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Tuition Reimbursement
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PTO accrual beginning Day 1
Note: Benefits may vary based upon position type and/or level.
Job Summary
The Clinical Research Supervisor oversees daily supervision of Clinical Research staff. This position develops, negotiates, and monitors budgets for funded research projects. It also facilitates the implementation of clinical research projects and ensures quality and timely completion.
Essential Functions of the Role
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Writes and assists in the development of proposals, grants, contracts, and budgets for the department.
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Assists in developing new protocols and materials from study sponsors. Provides input to Principal Investigators and management on clinical and research issues to establish financial and clinical feasibility.
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Assists various PIs, through delegated authority, in conducting clinical trials per federal, state, and institutional guidelines.
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Prepares initial project submissions, amendment notifications, SAE reports, continuing review reports, and other reports for the IRB. Reviews staff-prepared submissions to ensure they meet established standards.
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Oversees case report form completion by staff for all studies. Assists in coordinating audits by study sponsor monitors. Monitors assigned Clinical Research funds.
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Orientates, trains, supervises, and evaluates Clinical Research staff. Encourages growth through complex responsibilities and education programs. Coordinates project assignments for staff.
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Establishes and maintains good relations with the public, patients, and staff; promotes the department's research programs.
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Monitors communication with the IRB, Food and Drug Administration (FDA), and other applicable regulatory agencies.
Key Success Factors
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Research certification or other certifications per specialty area preferred.
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Basic Life Support (BLS) per department requirements.
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Proven written and oral communication skills.
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Proven computer skills, including Microsoft Office, Excel, and PowerPoint.
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Ability to manage time impressible projects in order to meet deadlines.
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Ability to establish and maintain effective working relationships.
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Excellent leadership skills.
Belonging Statement
We believe that all people should feel welcomed, valued and supported.
QUALIFICATIONS
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EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification
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EXPERIENCE - 2 Years of Experience
As a health care system committed to improving the health of those we serve, we are asking our employees to model the same behaviours that we promote to our patients. As of January 1, 2012, Baylor Scott & White Health no longer hires individuals who use nicotine products. We are an equal opportunity employer committed to ensuring a diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
How this job compares
Set against the 1,183 open Clinical Research jobs on Olive Jobs, counted October 31, 2026.
- Pay
- This postingNot listed
- Texas median$45–108K/yr21 salary ranges
- US median$25–35/hr168 hourly ranges
- Openings
- Olive Jobs lists 102 open Clinical Research jobs in Texas and 1,183 across the US. 11% of them nationwide are listed as remote or flexible.
- Hiring the most in Texas
- UNIVERSITY OF TEXAS AT AUSTIN30 open
- Houston Methodist22 open
- Iterative Health6 open
- Experience
- This posting asks for at least 2 years of experience; Clinical Research postings that state a minimum ask for 3 years at the median (826 postings).
- Education
- 463 of the 1,183 open Clinical Research jobs (39%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on October 31, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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