Clinical Research Coordinator I, Lab Trivedi

UT Southwestern Medical Center

Dallas (TX)

Presencial

USD 64.000 - 90.000

Jornada completa

Hace 3 días

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Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

PPO health plan

Paid time off

Parental leave

TRS retirement

Wellness programs

Tuition reimbursement

PSLF eligible

Descripción de la vacante

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support both clinical and basic research projects. You will coordinate patient visits, data collection, sample handling, and quality control under investigator supervision.

The ideal candidate has 1 year of clinical research experience, strong communication, and RedCap familiarity. Phlebotomy skills and IRB exposure are a plus; proficiency with Microsoft Office is required.

Formación

Education at least a Bachelor's degree in medical or science field.
1 year of clinical research experience preferred; more with advanced degree may be considered.
Experience with RedCap is preferred.
Phlebotomy experience is desirable.
Strong communication and organizational skills required.

Responsabilidades

Direct interaction with clinical research participants via in-person, phone, or telehealth.
Coordinate regulatory aspects and ensure compliance with policies and FDA requirements.
Schedule study procedures and manage protocol logistics with oversight from the PI.
Screen, recruit, enroll, and follow subjects per protocol guidelines.
Maintain data collection tools (CRFs) and assist with protocol development and budgeting.

Conocimientos

Clinical research experience

Interdisciplinary teamwork

Communication skills

Phlebotomy experience

RedCap experience

Strong organizational skills

Educación

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

Herramientas

RedCap

Microsoft Office Suite

Descripción del empleo

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 general supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.

The Preferred Candidate Would Possess The Following Qualifications/skills

Experience in both clinical and research study settings
Ability to work within an interdisciplinary team
Strong written and oral communication skills
Experience with Microsoft Office Suite
Strong organizational skills

Among Other Activities, The Position Will Be Responsible For

Direct interaction with clinical research participants enrolled in RAD/D2K (and possibly to include other studies)
Coordination of study procedures, activities, and payments
Collection of longitudinal study data and ensuring quality control of clinical research data
Overseeing patient retention
Supporting IRB maintenance and drafting of manuscripts and/or funding proposals
May be involved in sample collecting and processing

The ideal candidate will have a minimum of 2 years of experience working directly with participants/patients in clinical research studies. S/he will also be able to perform phlebotomy and have experience working with human tissue (including plasma, serum, and urine) specimens. Finally, experience working in Redcap is preferred.

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
Learn more about these and other UTSW employee benefits!

Required

EXPERIENCE AND EDUCATION

Education Bachelor's Degree or higher degree in medical or science related field
Experience 1 year of clinical research experience May consider additional years of experience or advanced degree in lieu of education or experience, respectively.

Preferred

Licenses and Certifications (BLS) BASIC LIFE SUPPORT Licensure may be required based on research study protocols or affiliate location requirements. (CPRAED) CPR AED Licensure may be required based on research study protocols or affiliate location requirements. ACRP or SOCRA certification a plus

Job Duties

Directly interacts with clinical research participants, as required, for the research study. Interacts via telephone, telehealth or in-person.
Coordinate regulatory aspects of the trial including maintaining and developing regulatory information to comply with industry standards, University policies, FDA requirements or other hospital policies
Coordinate and schedule study procedures as per protocol. Approved study protocols which have order sets built may be pended by the non-licensed coordinator with oversight by PI.
When outside of protocol, presents evidence and provides options (within scope of protocol) to PI.
Screen, recruit, enroll and follow subjects according to protocol guidelines. May also assist with the consent process
Maintain and coordinate data collection information required for each study which may also include developing CRF's or data collection tools
Assist in developing and implementing research studies to include writing clinical research protocols.
Conduct study procedures according to the protocol with proper training and check offs to maintain scope of work
Requires familiarity with research budgets to assist with or develop study budgets. May perform research billing activities, as needed, based on size of department (including linking patient calendars).
May review and abstract information from medical records for verification of eligibility for trials, as needed based on size of department.
Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards.
Review research study protocols to ensure feasibility
Assist in developing website or other social media for marketing/recruiting of clinical research study
Develop proficiency in the clinical trial management system, electronic medical record and other required data entry systems
Maintain subject level documentation
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.

Salary Information

Salary Is Commensurate With Education, Skills, And Relevant Experience.

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.

Primary Location

Texas-Dallas-5323 Harry Hines Blvd

Work Locations

5323 Harry Hines Blvd

Job

Research & Laboratory

Organization

426028 - PY-Lab Trivedi

Schedule

Full-time

Shift

Day Job