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Supervisor Clinical Research, Simmons Cancer Center

The University of Texas Southwestern Medical Center

Dallas (TX)

On-site

USD 70,000 - 90,000

Full time

3 days ago
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Job summary

UT Southwestern Medical Center seeks a Clinical Research Coordinator to oversee research projects. This role includes managing participant coordination, ensuring data accuracy, and leading a team in executing research protocols at a leading medical center in Dallas. Candidates should possess a Bachelor's degree and significant clinical research experience.

Benefits

PPO medical plan
Paid Time Off
Tuition Reimbursement
Wellness programs
Retirement Programs

Qualifications

  • 5 years of clinical research experience.
  • BLS and CPR certifications may be required.
  • Prior experience in UTSW clinical research mentoring program is a plus.

Responsibilities

  • Coordinate multiple complex research protocols.
  • Monitor patient safety and regulatory compliance.
  • Assure accurate data collection and timely submissions.

Skills

Clinical research
Patient interaction
Data management

Education

Bachelor's Degree in medical or science related field

Job description

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
Works under the direction of an Investigator(s) with limited supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Provides supervision to a team engaged in the execution of multiple, complex research protocols.

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
  • 100% coverage for preventive healthcare-no copay
  • 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
  • Learn more about these and other UTSW employee benefits!


EXPERIENCE AND EDUCATION
Required
  • Education

  • Bachelor's Degree in medical or science related field.
  • Experience

  • 5 years of clinical research experience.
    May consider additional years of experience or advanced degree in lieu of education or experience, respectively.
    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.
Preferred
  • 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.
    ACRP or SOCRA certification a plus.

JOB DUTIES
  • Assists with the daily operations for the research unit, to include but not limited to staffing, protocol management, budgeting, and regulatory requirements.
  • May assist in development of study design, implementation, and administration for new studies ensuring compliance with HRPP/IRB requirements, Federal/State regulations, and grant and/or contract parameters.
  • Assists with monitoring and oversight of active clinical research protocols in accordance with internal policies, federal and state regulations, and University policies.
  • Oversees and coordinates data collection and assures accuracy and timely submission to sponsors and/or external
  • Oversees and coordinates the scheduling and efficient usage of research facilities.
  • Performs research billing activities (including linking patient calendars) and oversees the financial status of the research protocols for the team
  • Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards
  • Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing, or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
  • Performs other duties as assigned.

SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information. To the extent this position requires the holder to research, work on, or have access to critical infrastructure as defined in Section 113.001(2) of the Texas Business and Commerce Code, the ability to maintain the security or integrity of the critical infrastructure is a minimum qualification to be hired and to continue to be employed in the position.

EEO Statement
UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.
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