Clinical Research Coordinator I , Psychiatry, Mood Disorders

UT Southwestern Medical Center; Dallas (TX); On-site; USD 50,000 - 65,000; Full time

Job summary

UT Southwestern Medical Center seeks a Clinical Research Coordinator I for its Mood Disorders Division. The role involves coordinating clinical trials, ensuring regulatory compliance, and managing participant interactions. Ideal candidates hold a Bachelor's degree in a medical or related field and have clinical research experience.

Benefits

PPO medical plan with no cost for employee-only coverage

100% coverage for preventive healthcare

Paid Time Off available from day one

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF) Qualified Employer

Qualifications

• Requires 1 year of clinical research experience.
• Knowledge of BLS and CPR certification may be required.
• ACRP or SOCRA certification is a plus.

Responsibilities

• Coordinate regulatory aspects of clinical trials and maintain compliance.
• Directly interact with clinical research participants and manage data collection.
• Recruit and enroll subjects as per study protocols.

Skills

Communication

Teamwork

Organization

Regulatory Compliance

Education

Bachelor's Degree in a medical or science related field

Job description

Clinical Research Coordinator I - Psychiatry Department - Mood Disorders Division

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

The Mood Disorders Division of the Pschiatry Department is looking to hire a full time Clinical Research Coordinator I. This position is intended to serve as one of the primary coordinators at UT Southwestern for the ongoing Ketamine for Methamphetamine Use Disorder (KMD) trial. The coordinator will work closely with the site PI, site clinicians, coordinator, Clinical Research Unit staff, consulting cardiologist, and other team members in executing all aspects of the ongoing research study. This position will also work closely with members of the Big Southwest Node and of the KMD Lead Team to ensure that UTSW as a site is compliant with all the regulatory requirements, study site deliverables of the study. In addition these regulatory requirements will include site level maintenance of IRB protocol (with BRANY as sIRB as well as UTSW as local reliant IRB). Furthermore, this position is responsible for optimizing the resources available such as working with a multidisciplinary team including other study staff/medical clinicians, recruitment/retention specialist, external recruitment companies etc. to meet the recruitment goals assigned by the Lead Team of KMD.

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 or higher degree in medical or science related field

• Experience
  1 year clinical research experience

Preferred

• Education
  May consider additional years of experience or advanced degree in lieu of education or experience, respectively.

• 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 certifiction 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.

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.