Lead CRC: Computational Psychiatry & Wearables

UT Southwestern Medical Center; Dallas (TX); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

PPO medical plan day one for full-time

Paid Time Off from day one

Retirement Programs (TRS)

Paid Parental Leave

Wellness programs

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF)

Job summary

UT Southwestern Medical Center in Dallas, TX is seeking a CRC Lead to coordinate longitudinal research studies involving wearable sensor data and clinical outcomes. The role centers on screening, recruiting, enrolling participants, obtaining informed consent, and administering standardized assessments.

The ideal candidate has a bachelor’s degree in a medical/science field and at least four years of clinical research experience; familiarity with REDCap, EPIC, ETHOS, Velos, Florence, and Microsoft

Qualifications

• Education Bachelor's Degree in medical or science related field
• Experience 4 years of clinical research experience with Bachelor's Degree; prior experience in the UT Southwestern clinical research mentoring program is highly desirable; may count as additional experience.
• May consider additional years of experience or advanced degree in lieu of education or experience, respectively.

Responsibilities

• Maintains required subject documentation for each study protocol.
• Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Interacts via telephone, telehealth or in-person.
• Coordinates regulatory documentation for research studies that includes maintaining information to comply with industry standards, University policies, FDA requirements or other hospital policies.
• Coordinates and schedules procedures as per research study.
• Screens, recruits, enrolls and follows subjects according to research protocol guidelines (non-clinical and clinical procedures).
• Maintains and coordinates data collection information required for each study that may also include developing CRF's or data collection tools.
• Assists in developing and implementing research studies, may include writing clinical research protocols.
• Conducts research procedures according to the protocol with proper training and check offs to maintain scope of service.
• May provide supervision to other members of the research team as necessary.
• May perform research billing activities, as needed, based on size of department.
• Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards.
• Assists PI/supervisor with daily activities of the research team and functions as a liaison between clinical research investigators and various organizations/departments and agencies including HRPP, FDA, Sponsored Programs, and affiliated hospitals.
• Coordinates data management and collection for national (larger/more complex) research studies.
• Serves as lead in preparing annual reports for federal, state, and or local agencies on assigned studies.
• Prepares protocols for Institutional Review Board (IRB) submission. May also submit amendments and continuing review documents.
• Assists and monitors and/or maintain research study budgets. Assists the PI with the fiscal management of the trial. Ensures that the patient care charges are allocated appropriately for various research studies.
• Provides in-service training to all study team members and communicates to involved groups.
• Reviews research study protocols to ensure feasibility requirements of the study.
• Assists in developing website or other social media for marketing/recruiting based on assigned clinical research study.
• Enters data in the assigned clinical trial management system, electronic medical record and/or other required data entry systems.
• 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; or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
• Performs other duties as assigned.

Skills

REDCap

EPIC

ETHOS

Velos

Florence

Microsoft Office

Education

Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center in Dallas, TX is seeking a CRC Lead to coordinate longitudinal research studies involving wearable sensor data and clinical outcomes. The role centers on screening, recruiting, enrolling participants, obtaining informed consent, and administering standardized assessments.

The ideal candidate has a bachelor’s degree in a medical/science field and at least four years of clinical research experience; familiarity with REDCap, EPIC, ETHOS, Velos, Florence, and Microsoft