UT Southwestern Medical Center
Lead Clinical Research Coordinator, Ophthalmology CRU
UT Southwestern Medical Center, Dallas, Texas, United States, 75215
Lead Clinical Research Coordinator - Ophthalmology Clinical Research Unit (CRU)
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 Clinical Research Unit of the Ophthalmology Department is looking to hire a full time Lead Clinical Research Coordinator. The CRC Lead will be based at the Clinical Research Unit (CRU) in the Ophthalmology Department and will play a critical role in coordinating and supporting clinical research activities. In addition to fulfilling all Clinical Research Assistant I (CRA I) responsibilities, the CRC Lead will provide direct patient care by performing detailed ophthalmic examinations such as taking medical histories, medication reconciliation, visual acuity assessments (including BCVA, ETDRS), motility, pupils, confrontation fields, tonometry, refractions, lensometry, specular microscopy, and administering ophthalmic drops. The role also involves conducting ophthalmic imaging using both standard and investigational devices including Heidelberg OCT, Optovue OCT-A, Oculus Pentacam, and other research-specific technologies, all in accordance with study protocols. The CRC Lead is expected to learn and implement new techniques, especially in ophthalmic photography, and will be responsible for training team members on study-specific procedures and equipment use. As the primary CRC on assigned studies, this role will oversee and guide research personnel, ensuring that all processes align with CRU operations in collaboration with the Clinical Research Manager (CRM). The CRC Lead will participate actively in all studies, assist in decision-making under CRM supervision, and contribute to building a strong, functional, and adaptive team by stepping in wherever needed. Responsibilities also include coordination of research studies, timely and accurate data entry into EDC systems, maintenance of regulatory binders, patient EHR updates, and ensuring HIPAA compliance. Additional duties involve reviewing physician schedules, coordinating referrals, maintaining patient records, onboarding new hires, managing medical supplies, troubleshooting and calibrating ophthalmic equipment, ensuring certification of instruments, assisting with planning and developing CRU operations, and supporting initiatives to improve workflow and enhance the research participant experience. A background in extensive ophthalmic clinical research with knowledge and proficiency in ophthalmic techniques for clinical research is strongly preferred, along with experience supporting both internal and external clinical studies.
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 in medical or science related field
Experience 4 years of clinical research experience with Bachelor's Degree Prior experience in the UTSW clinical research mentoring program is highly desirable, and participation in the UTSW clinical research mentoring program may count as additional 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 may be required based on research study protocols or affiliate location requirements. (CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements. ACRP of SOCRA certification a plus.
JOB DUTIES
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. A non-licensed coordinator may pend study order sets with oversight by PI.
Screens, recruits, enrolls and follows subjects according to research protocol guidelines (non-clinical and clinical procedures). May also assist with the consent processes.
Maintains and coordinates data collection information required for each study that may also include developing CRF's (case report form) 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 (including linking patient calendars
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, but not limited to 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/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 (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. 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!
JOB SUMMARY The Clinical Research Unit of the Ophthalmology Department is looking to hire a full time Lead Clinical Research Coordinator. The CRC Lead will be based at the Clinical Research Unit (CRU) in the Ophthalmology Department and will play a critical role in coordinating and supporting clinical research activities. In addition to fulfilling all Clinical Research Assistant I (CRA I) responsibilities, the CRC Lead will provide direct patient care by performing detailed ophthalmic examinations such as taking medical histories, medication reconciliation, visual acuity assessments (including BCVA, ETDRS), motility, pupils, confrontation fields, tonometry, refractions, lensometry, specular microscopy, and administering ophthalmic drops. The role also involves conducting ophthalmic imaging using both standard and investigational devices including Heidelberg OCT, Optovue OCT-A, Oculus Pentacam, and other research-specific technologies, all in accordance with study protocols. The CRC Lead is expected to learn and implement new techniques, especially in ophthalmic photography, and will be responsible for training team members on study-specific procedures and equipment use. As the primary CRC on assigned studies, this role will oversee and guide research personnel, ensuring that all processes align with CRU operations in collaboration with the Clinical Research Manager (CRM). The CRC Lead will participate actively in all studies, assist in decision-making under CRM supervision, and contribute to building a strong, functional, and adaptive team by stepping in wherever needed. Responsibilities also include coordination of research studies, timely and accurate data entry into EDC systems, maintenance of regulatory binders, patient EHR updates, and ensuring HIPAA compliance. Additional duties involve reviewing physician schedules, coordinating referrals, maintaining patient records, onboarding new hires, managing medical supplies, troubleshooting and calibrating ophthalmic equipment, ensuring certification of instruments, assisting with planning and developing CRU operations, and supporting initiatives to improve workflow and enhance the research participant experience. A background in extensive ophthalmic clinical research with knowledge and proficiency in ophthalmic techniques for clinical research is strongly preferred, along with experience supporting both internal and external clinical studies.
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 in medical or science related field
Experience 4 years of clinical research experience with Bachelor's Degree Prior experience in the UTSW clinical research mentoring program is highly desirable, and participation in the UTSW clinical research mentoring program may count as additional 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 may be required based on research study protocols or affiliate location requirements. (CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements. ACRP of SOCRA certification a plus.
JOB DUTIES
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. A non-licensed coordinator may pend study order sets with oversight by PI.
Screens, recruits, enrolls and follows subjects according to research protocol guidelines (non-clinical and clinical procedures). May also assist with the consent processes.
Maintains and coordinates data collection information required for each study that may also include developing CRF's (case report form) 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 (including linking patient calendars
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, but not limited to 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/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 (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. 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!