Project Manager 3 – Clinical Research & Healthcare Programs

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 We serve faithfully by doing what's right with a joyful heart. We never settle by constantly striving for better. We are in it together by supporting one another and those we serve. 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:

• 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.

Job Summary

We are seeking an experienced and highly organized Project Manager to lead a national, multi-site clinical research consortium focused on improving outcomes for individuals with chronic kidney disease. This role provides operational leadership for a large pragmatic clinical trial and related stakeholder engagement, implementation science, and data coordination activities across multiple health systems and academic institutions.

Responsibilities

Responsibilities include:

• Coordinating consortium operations
• Managing project timelines and deliverables
• Facilitating communication among participating sites and research cores
• Supporting regulatory and contractual activities
• Monitoring study progress
• Ensuring compliance with sponsor requirements

Essential Functions Of The Role

The essential functions of the role include:

• Coordinate day-to-day operations of a national, multi-site clinical research consortium
• Develop and maintain project plans, timelines, milestones, and deliverable tracking systems
• Facilitate communication and collaboration among investigators, research coordinators, data teams, stakeholder partners, and external collaborators
• Organize and support Steering Committee, investigator, stakeholder, and site coordinator meetings, including agenda preparation, meeting minutes, and follow-up actions
• Monitor study progress, enrollment performance, milestone achievement, and sponsor reporting requirements
• Support implementation of study protocols across participating sites and assist with resolving operational challenges
• Coordinate activities related to regulatory approvals, contracts, subawards, and data use agreements
• Prepare reports, presentations, and project updates for investigators, sponsors, and oversight committees
• Collaborate with finance and grants management teams to monitor project budgets and ensure compliance with sponsor requirements
• Serve as a central point of contact for participating institutions and research partners
• Maintain project documentation and ensure compliance with organizational, regulatory, and sponsor policies

Qualifications

Minimum qualifications:

• Minimum of 5 years of clinical project management related experience required

Preferred qualifications:

• Master's degree in Public Health, Healthcare Administration, Clinical Research, Business Administration, or related field
• Experience supporting clinical research, healthcare operations, academic medicine, or grant-funded programs preferred
• Project Management Professional (PMP) certification
• Experience managing multicenter clinical research studies, clinical trials, or research networks
• Experience coordinating projects across multiple institutions or clinical sites
• Experience with federally funded, foundation-funded, or industry-sponsored research programs
• Experience working with physicians, principal investigators, research coordinators, and healthcare leadership
• Experience in academic medicine, clinical research administration, or healthcare research operations
• Knowledge of clinical research regulations, IRB processes, and Good Clinical Practice (GCP)
• Experience with REDCap, clinical trial management systems, and other research platforms

Pay

The pay range for this position is $40.35 (entry-level qualifications) - $62.52 (highly experienced). The specific rate will depend upon the successful candidate’s specific qualifications and prior experience.

Belonging Statement

We believe that all people should feel welcomed, valued and supported.