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Clinical Research Manager, Simmons Cancer Center

Job in Dallas, Dallas County, Texas, 75215, USA
Listing for: The University of Texas Southwestern Medical Center
Full Time position
Listed on 2026-01-10
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Job Description & How to Apply Below

Job Description - Clinical Research Manager, Simmons Cancer Center (913090)

Job Description

Clinical Research Manager, Simmons Cancer Center - (913090)

Description

Clinical Research Manager - Simmons Cancer Center - Neuro-Oncology Division

WHY UT SOUTHWESTERN? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals.

Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!

JOB SUMMARY The Clinical Research Manager is responsible for the overall Neuro-Oncology Disease Oriented Team (Use the "Apply for this Job" box below). functions and includes working closely with DOT leaders to manage pipeline of studies, organizing monthly DOT meetings and assisting in the development of investigator-initiated trials. Additionally, manages coordination of staff, which includes hiring, initial training and onboarding, continuing education and development as well as performance management.

This role also provides oversight of study start-up activities, which includes managing the progress of new trials through regulatory approval, contract and budgeting as well as ancillary reviews. Additional responsibilities include general study management activities such as monitoring accrual, facilitating continuing review, maintaining relationships with sponsor, pharmacy, ancillary and clinic staff and playing an active role in quality assurance by participating in internal audits and implementation of corrective actions as required.

This role also requires the incumbent to maintain the ability to function as a study coordinator when required.

BENEFITS UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

  • PPO medical plan, available day one at no cost for full-time employee-only coverage
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer
  • Education Bachelor's Degree in science, social science, business, health-related (including nursing) field or Master’s Degree in science, social science, business, or health-related (including nursing) field or PhD or equivalent in science, social science, business, or health-related (including nursing) field
  • Experience 6 years of related experience to include management experience with Bachelor's Degree or 4 years of related experience to include management experience with Master's Degree or 3 years of related experience to include management experience with PhD.

Preferred

Experience Prior experience in the UTSW clinical research mentoring program is highly desirable, and participation in the UTSW clinical research mentoring program may count as additional experience.

Previous Neuro-Oncology Coordinating experience

Previous Study start-up experience

  • Licenses and Certifications (BLS) BASIC LIFE SUPPORT may be required based on research study protocols or affiliate location requirements. (CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements.

JOB DUTIES

  • Reviews proposed new research studies and determines projects to implement; negotiates budget and contract issues; initiates regulatory activities; oversees preparation of necessary project summaries, consent forms, etc. for IRB; oversees compliance with all regulatory requirements.
  • Oversees on-going research studies and quality assurance measures, developing criteria where necessary; negotiates…
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