Clinical Research Assistant Lead, Internal Medicine

UT Southwestern Medical Center; Dallas (TX); Sur place; USD 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

PPO medical plan

Paid Time Off

Retirement Programs through the TRS

Paid Parental Leave Benefit

Wellness programs

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF)

Résumé du poste

UT Southwestern Medical Center in Dallas seeks a data management professional to support local and national research studies. The role coordinates patient participation, visits, data quality, and regulatory compliance under PI supervision.

The ideal candidate has experience in clinical research coordination, data entry, and familiarity with phlebotomy or related procedures. This on-site position offers comprehensive benefits and career development opportunities.

Qualifications

• High School Diploma or higher in medical or science field.
• Experience requirements vary by degree level (4/2/1 years).
• Prior UTSW clinical research mentoring is desirable.

Responsabilités

• Assist with participant screening and recruitment for complex trials.
• Obtain and document consent for study participants.
• Enter and verify data in case report forms and data systems.
• Coordinate study visits and ensure protocol adherence.
• Maintain study documentation and regulatory filings.
• Support with specimen collection and basic patient care per scope.

Connaissances

Data management

Clinical research coordination

Phlebotomy

Data entry

Regulatory knowledge

Formation

High School Diploma

Associate's Degree in medical or science-related field

Bachelor's Degree or higher in medical or science-related field

Outils

EHR systems

Data entry software

Description du poste

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 No. 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 provide ongoing data management for local and national research studies and may coordinate observational (non-treatment/treatment) trials/studies. Works on complex studies in a lead role, under the direction of the PI and/or Clinical Research Coordinator.

Works under the direction of Investigators and the Research program manager with limited supervision to coordinate clinical research projects. The position primarily coordinates patient participation, research visits, conduct data management and ensures the quality control of clinical research data is support of multiple drug, device or biorepository complex research studies in Pulmonary hypertension, Interstitial lung diseases, Lung transplant, Interventional Pulmonology and COPD.

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

• High School Diploma or
• Associate's Degree in medical or science related field or
• Bachelor's Degree or higher in medical or science related field

Experience

• 4 years of experience with High School Diploma or
• 2 years of experience with Associate's Degree or
• 1 year of experience with Bachelor's Degree or higher

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 protocol or affiliate location requirements.
• (CPRAED) CPR AED may be required based on research study protocol or affiliate location requirements.

JOB DUTIES

• Assists with participant screening and recruitment for complex trials or multiple research studies at any given time.
• Conducts and documents consent for participants in studies. Develops consent plans and documents for participants.
• Independently corrects and documents incomplete, inaccurate, or missing data for more complex studies.
• Understands visit schedules, criteria and protocol requirements for complex trials; schedules research visits, etc.
• Completes research protocol related tasks.
• Reviews and abstracts information from medical records including eligibility criteria.
• Recruits and enrolls patients in research study that may include consenting patients.
• Enters data into case report forms or other data collection system based on research study. Assists with maintenance of study level documentation.
• Assists with data queries and possible edits for accuracy.
• Compiles data for regulatory requirements and /or deadlines for local or sponsor submissions.
• Maintains existing databases and ensures data integrity.
• Assists with ordering and maintaining research supplies following university/department procedures, ensuring that equipment is in good working order.
• Assists with collecting and processing specimens following established procedures/protocols.
• With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG's needed for research study. Based on research study, other procedures/equipment/services may be required.
• May perform patient care (basic skills) under the direction of PI following scope of work document.
• 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, modif