Visiting Jr. Researcher, Dermatology

UT Southwestern Medical Center • Dallas, TX

1d

About The Position

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! 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 Working on a fellowship or post-degree education with no experience. JOB DUTIES The Clinical Research Fellow supports the successful conduct of clinical research studies under the direction of the Director of Clinical Trials and the supervision of a faculty Principal Investigator (PI). This role is responsible for active participation in all phases of clinical trial execution, including protocol implementation, patient-facing research activities, data and documentation management, and support for investigator-initiated research. The Clinical Research Fellow also contributes to the academic mission of the research program through mentorship, scholarly support, and collaboration with faculty, research staff, and learners. Key Responsibilities Protocol and Study Training Complete all required institutional, sponsor, and protocol-specific training related to assigned clinical research studies Maintain familiarity with study procedures, eligibility criteria, safety reporting requirements, and PI-specific expectations Remain current on applicable research compliance and Good Clinical Practice standards Clinical Trial Conduct Participate fully in the execution of clinical trials under faculty supervision Perform protocol-required efficacy and safety assessments Conduct physical examinations and obtain relevant medical histories, as appropriate to the study protocol and level of training Recruit, screen, and consent potential study participants Coordinate and manage baseline, follow-up, and final study visits Identify, document, and report adverse events and other safety data in accordance with protocol, sponsor, and regulatory requirements Enter study data into electronic case report forms (eCRFs) accurately and in a timely manner Maintain complete and accurate source documentation Assist in resolving data queries and discrepancies as applicable Attend investigator meetings, sponsor meetings, and monitoring visits as needed Sample Processing and Study Support Assist with the collection, processing, packaging, and shipment of research samples in accordance with protocol and laboratory requirements Support day-to-day study operations to ensure timely and compliant study execution Investigator-Initiated Research and Registries Support faculty and study teams in the development of investigator-initiated study protocols and informed consent documents Assist with Institutional Review Board (IRB) submissions, modifications, and related regulatory documentation Provide support for contract coordination and study start-up activities, as needed Contribute to the preparation of presentations, abstracts, posters, and manuscripts related to clinical research activities Education and Mentorship Provide guidance, support, and mentorship to students participating in clinical research activities Promote a collaborative learning environment within the clinical research program Document Review and Quality Support Assist with the review of translated protocols, informed consent forms, and related study materials for accuracy, completeness, and clarity Support quality and consistency in research documentation and communications 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. EEO 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.

Requirements

• Working on a fellowship or post-degree education with no experience.

Responsibilities

• Complete all required institutional, sponsor, and protocol-specific training related to assigned clinical research studies
• Maintain familiarity with study procedures, eligibility criteria, safety reporting requirements, and PI-specific expectations
• Remain current on applicable research compliance and Good Clinical Practice standards
• Participate fully in the execution of clinical trials under faculty supervision
• Perform protocol-required efficacy and safety assessments
• Conduct physical examinations and obtain relevant medical histories, as appropriate to the study protocol and level of training
• Recruit, screen, and consent potential study participants
• Coordinate and manage baseline, follow-up, and final study visits
• Identify, document, and report adverse events and other safety data in accordance with protocol, sponsor, and regulatory requirements
• Enter study data into electronic case report forms (eCRFs) accurately and in a timely manner
• Maintain complete and accurate source documentation
• Assist in resolving data queries and discrepancies as applicable
• Attend investigator meetings, sponsor meetings, and monitoring visits as needed
• Assist with the collection, processing, packaging, and shipment of research samples in accordance with protocol and laboratory requirements
• Support day-to-day study operations to ensure timely and compliant study execution
• Support faculty and study teams in the development of investigator-initiated study protocols and informed consent documents
• Assist with Institutional Review Board (IRB) submissions, modifications, and related regulatory documentation
• Provide support for contract coordination and study start-up activities, as needed
• Contribute to the preparation of presentations, abstracts, posters, and manuscripts related to clinical research activities
• Provide guidance, support, and mentorship to students participating in clinical research activities
• Promote a collaborative learning environment within the clinical research program
• Assist with the review of translated protocols, informed consent forms, and related study materials for accuracy, completeness, and clarity
• Support quality and consistency in research documentation and communications

Benefits

• 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

What This Job Offers

• Career Level: Entry Level
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees