Clinical Research Coordinator I, Internal Medicine Cardiology
for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we need to decide which sections to include based on content.
We have:
- About the role: could combine "Why UT Southwestern?" and Job Summary. That's substantive.
- Responsibilities: Job Duties (list). Could be Responsibilities.
- Requirements: Required EXPERIENCE AND EDUCATION.
- Qualifications: maybe Preferred Licenses and Certifications? Or could be Qualifications.
- Skills: maybe not explicit; we could omit if no specific skills listed besides those in duties. Could omit.
- Benefits: we have Benefits section.
- Pay: not present, omit.
- Schedule: we have Full-time, Day shift.
Also location maybe not needed as heading; could be included in About the role paragraph.
We must not repeat job title. No Job ID etc.
We must output only HTML fragment, no /, no markdown fences.
We need to use - for any list of duties/requirements/benefits. Use
for prose.
We need to preserve ALL substantive information; do not invent or summarize away detail. So we need to keep all details from the posting, but we can format them.
We must remove boilerplate: EEO, security statement, etc. Also remove duplicated lines, navigation, cookie, legal, scam-warning, application instructions. There's no explicit application instructions but we should remove any like "Learn more about these and other UTSW employee benefits!" maybe that's okay as part of benefits? It's not boilerplate; it's a call to action but maybe considered application instruction? It's about benefits; we can keep it as part of benefits description.
We need to ensure we don't include placeholders like "commensurate with experience". Not present.
Let's extract content:
Why UT Southwestern? paragraph:
"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:
"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."
Benefits:
"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 coverage100% coverage for preventive healthcare-no copayPaid Time Off, available day oneRetirement Programs through the Teacher Retirement System of Texas (TRS)Paid Parental Leave BenefitWellness programsTuition ReimbursementPublic Service Loan Forgiveness (PSLF) Qualified EmployerLearn more about these and other UTSW employee benefits!"
We need to format as list.
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: a long list. We need to turn into
- items. Must preserve all details. Let's parse the duties paragraph:
"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 policiesCoordinate 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 processMaintain and coordinate data collection information required for each study which may also include developing CRF's or data collection toolsAssist 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 workRequires 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 feasibilityAssist in developing website or other social media for marketing/recruiting of clinical research studyDevelop proficiency in the clinical trial management system, electronic medical record and other required data entry systemsMaintain subject level documentationDuties 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."
We need to split into sensible list items. Could keep each sentence as an item. Also include the core functions as subitems? But we just need list; we can keep them as separate items.
Schedule: "Full-time Shift Day". Also location maybe not needed.
We need to avoid duplication: The "Job Summary" and "Why UT Southwestern?" both have some overlapping benefits mention; but we keep both.
Now construct HTML:
About the role
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: 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.
Responsibilities
- 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.
Requirements
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.
Qualifications
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.
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
for prose. We need to preserve ALL substantive information; do not invent or summarize away detail. So we need to keep all details from the posting, but we can format them. We must remove boilerplate: EEO, security statement, etc. Also remove duplicated lines, navigation, cookie, legal, scam-warning, application instructions. There's no explicit application instructions but we should remove any like "Learn more about these and other UTSW employee benefits!" maybe that's okay as part of benefits? It's not boilerplate; it's a call to action but maybe considered application instruction? It's about benefits; we can keep it as part of benefits description. We need to ensure we don't include placeholders like "commensurate with experience". Not present. Let's extract content: Why UT Southwestern? paragraph: "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: "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." Benefits: "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 coverage100% coverage for preventive healthcare-no copayPaid Time Off, available day oneRetirement Programs through the Teacher Retirement System of Texas (TRS)Paid Parental Leave BenefitWellness programsTuition ReimbursementPublic Service Loan Forgiveness (PSLF) Qualified EmployerLearn more about these and other UTSW employee benefits!" We need to format as list. 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: a long list. We need to turn into
- items. Must preserve all details. Let's parse the duties paragraph:
"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 policiesCoordinate 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 processMaintain and coordinate data collection information required for each study which may also include developing CRF's or data collection toolsAssist 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 workRequires 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 feasibilityAssist in developing website or other social media for marketing/recruiting of clinical research studyDevelop proficiency in the clinical trial management system, electronic medical record and other required data entry systemsMaintain subject level documentationDuties 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."
We need to split into sensible list items. Could keep each sentence as an item. Also include the core functions as subitems? But we just need list; we can keep them as separate items.
Schedule: "Full-time Shift Day". Also location maybe not needed.
We need to avoid duplication: The "Job Summary" and "Why UT Southwestern?" both have some overlapping benefits mention; but we keep both.
Now construct HTML:
About the role
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: 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.
Responsibilities
- 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.
Requirements
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.
Qualifications
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.
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