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Form of workClinical Research Coordinator I - Psychiatry Department - Mood Disorders Division Departmental Job Description
At UT Southwestern's Center for Depression Research and Clinical Care (CDRC), we believe that a future free from the burden of emotional and behavioral disorders is possible. Our mission is exemplified by the extensive research done in the center on methods to prevent and treat depression and associated disorders, including bipolar, anxiety, and substance use disorders.
The Psychiatry Department is looking to hire a Clinical Research Coordinator I to assist with their ongoing clinical trials and studies. This position will manage multiple projects related to the Texas-Youth Depression and Suicide Research Network (TX-YDSRN) in the Center for Depression Research and Clinical Care (CDRC). Duties will include:
Coordinating the implementation of projects and related trainings.
Oversee Clinical Research operations. Develop training and program materials
Assisting in conducting psychosocial interventions (including behavioral activation) and clinical assessments
Train and support interventionists to implement psychosocial interventions
Overseeing project IRBs Establishing and maintaining relationships with network partners
Working with interventionists to ensure program fidelity
Attend trainings and weekly meetings to discuss success and obstacles of different projects
Bachelor's or higher degree in medical or science related field and one-year Clinical Research experience.
May consider additional years of experience or advanced degree in lieu of education or experience, respectively.
ACRP or SOCRA certification a plus.
A Heart Saver for non-licensure or BLS for Licensure may be required based on research study protocols or affiliate location requirements.
May perform some or all the following:
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.
Work requires knowledge of basic and Clinical Research terminology, regulations, and procedures.
Work requires strong computer skills (spreadsheets, databases, and interactive web-based software).
Work requires ability to communicate effectively with various levels of internal and external contacts.
Work requires ability to work with confidential information on daily basis
Proactively works to maximize results of the team and organization
Follows and understands the regulations for Protected Health Information (PHI)
Work requires good communication skills.
Work requires the ability to problem solve.
- Work is performed primarily in office environment but may require periodic visits to clinic areas for purpose of interviewing patients.
For COVID-19 vaccine information,applicants should visithttps://www.utsouthwestern.edu/covid-19/work-on-campus/
To learn more about the benefits UT Southwestern offers, visit https://www.utsouthwestern.edu/employees/hr-resources/
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information
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.
To learn more, please visit: https://jobs.utsouthwestern.edu/why-work-here/diversity-inclusion
