Clinical Research Technician/Clinical Research Assistant - Term Limited

We need to output HTML fragment with sections: headings

for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. We must not repeat job title. Must preserve all substantive info, not invent or summarize away detail. Remove boilerplate like "How to Apply", "Mission Statement", "Job Summary" duplicates, "Why Join Michigan Medicine?" maybe not needed unless it's substantive? It's more marketing; but we need to preserve all substantive information. The instruction: "Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions." So we should remove "How to Apply" and "Mission Statement" maybe? Mission statement is not boilerplate? It's about organization; could be considered not required but maybe we keep? The instruction says remove duplicated lines, application instructions. Mission statement is not duplicated but maybe not essential? However we need to preserve ALL substantive information. The mission statement is substantive about the organization; but not about the role. The instruction: "Prefer a few substantive sections over many thin ones." We can include an "About the role" section summarizing the job summary. The job summary includes details about CPFRC, responsibilities, etc. We'll need to extract responsibilities list, qualifications, desired qualifications, benefits, work schedule, etc. We must not create Pay/Schedule/Benefits sections unless posting actually states them. Benefits: there is a section "What Benefits can you Look Forward to?" with bullet points: Excellent medical, dental and vision coverage effective on your very first day; 2:1 Match on retirement savings. Also "Modes of Work Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department." That's about work mode. Also "Work Schedule This position will be on site to begin and will be eligible for a hybrid work schedule combining remote and in-office work. The position is a 40-hr/week role." So we have schedule and benefits. We must not include sections with filler like "commensurate with experience". Not present. We need to output only HTML fragment, no /, no markdown fences. We'll structure:

About the role

... job summary ...

Responsibilities

• ... list items ...

Required Qualifications

• ... list items ...

Desired Qualifications

• ... list items ...

Benefits

• ... list items ...

Work Schedule

... schedule info ...

We must ensure we don't duplicate content. Let's extract substantive content. From posting: Job Summary (duplicate of How to Apply). We'll combine. "The Chronic Pain and Fatigue Research Center (CPFRC), located within the Department of Anesthesiology is a collaborative, collegial, and fast paced program that enjoys the opportunity to partner with many researchers from the Schools of Medicine and Public Health, as well as extramural biomedical researchers. The successful candidate for this position will participate in many aspects of research analysis and collaborative activities, with research programs including longitudinal cohorts, cross-sectional studies, clinical trials, health services and translational research with funding from a variety of sponsors including, NIH, industry, and others. The CPFRC provides rich opportunities for career development and continued learning from experienced colleagues. The research team includes physicians, biostatisticians, project managers, study coordinators, data managers, and administrative support. The Clinical Study Coordinator-Technician is expected to work as part of a collaborative team and is responsible for managing their assigned tasks. They are expected to understand and support the conduct of research within all federal, state, and local regulatory requirements. This position provides administrative and coordination support for multiple projects in the conduct of clinical research projects. Assignments may include tasks for both single-center and multi-center studies. This position may independently provide study coordination for simple and moderately complex clinical research studies. As a member of a coordination team, this position will help support a portfolio of projects with varying levels of complexity." That's good for About the role. Responsibilities: list under "Characteristic Duties And Responsibilities". We need to extract bullet points. The text after "Responsibilities* Characteristic Duties And Responsibilities Knowledge of all 8 competency domains is expected: Scientific Concepts and Research DesignEthical Participant Safety ConsiderationsInvestigational Products Development and RegulationClinical Study Operations (GCPs)Study and Site ManagementData Management and InformaticsLeadership and ProfessionalismCommunication and TeamworkProvide support to participants around the multiple technological components of research studies and trials, including installing the study smartphone application(s), electronic consenting, and setup of wearable devices, as well as navigating online electronic data capture systems. CRC-tech will work with other team members to:organize and reach out to lists of participants that may be contacted for recruitment,Screen, informed consent, and enrollment of participants according to protocol for research studies,track and follow participants in study after their initial enrollment,enter and manage data,conduct chart reviews as necessary,prepare and send participant mailings,support the distribution of participant incentives,provide customer support around participant usage of the studies? technologiesperform other routine project tasks. Assist with maintaining regulatory documents and assisting with IRB submissions such as amendments, SAEs and ORIOs.May assist in the preparation of a variety of reports such as quarterly updates and regulatory.Help build and maintain participant databases for remote data collection and participant scheduling, tracking, and monitoring, including resolving data queriesAttend regular team meetings to discuss, troubleshoot and resolve study activitiesTravel (5-10%) may be required to participant in necessary meetingsOther duties as assigned" We need to split into list items. We'll create items: - Knowledge of all 8 competency domains is expected: Scientific Concepts and Research Design; Ethical Participant Safety Considerations; Investigational Products Development and Regulation; Clinical Study Operations (GCPs); Study and Site Management; Data Management and Informatics; Leadership and Professionalism; Communication and Teamwork. - Provide support to participants around the multiple technological components of research studies and trials, including installing the study smartphone application(s), electronic consenting, and setup of wearable devices, as well as navigating online electronic data capture systems. - Organize and reach out to lists of participants that may be contacted for recruitment. - Screen, informed consent, and enrollment of participants according to protocol for research studies. - Track and follow participants in study after their initial enrollment. - Enter and manage data. - Conduct chart reviews as necessary. - Prepare and send participant mailings. - Support the distribution of participant incentives. - Provide customer support around participant usage of the studies' technologies. - Perform other routine project tasks. - Assist with maintaining regulatory documents and assisting with IRB submissions such as amendments, SAEs and ORIOs. - May assist in the preparation of a variety of reports such as quarterly updates and regulatory. - Help build and maintain participant databases for remote data collection and participant scheduling, tracking, and monitoring, including resolving data queries. - Attend regular team meetings to discuss, troubleshoot and resolve study activities. - Travel (5-10%) may be required to participate in necessary meetings. - Other duties as assigned. We need to ensure we don't duplicate. Required Qualifications: list after "Required Qualifications*". The text: "Performs moderately complex study procedures with accuracyAbility to work independently but also within a teamJob will require flexibility in order to meet project deadlines and goals; therefore, a strong ability to problem-solve is highly desiredThe candidate for this position must also be able to adhere to strict confidentiality guidelines, demonstrate a strong ability to establish rapport with participants, and demonstrate a strong ability to keep accurate and detailed records of all study procedures.Experience with Microsoft Office products (i.e., Microsoft Word, Excel, and Power Point) Confident and highly motivated with excellent multi-tasking ability and record-keeping skills. Outstanding organizational skills with meticulous attention to detail. Strong ability to work independently, exercising good judgement, with minimal supervision. Demonstrated ability to learn and use new skills quickly and effectively. Able to maintain data confidentiality and adhering to participant privacy. Clinical Research Technician Associate degree in Health Science or an equivalent combination of related education and experience is necessary. Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRAs Definition of a Clinical Research Professional for qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. orMinimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research. Clinical Research Assistant High school diploma or GED is necessary." We need to parse into list items. It's a bit messy. Let's extract distinct qualifications: - Performs moderately complex study procedures with accuracy. - Ability to work independently but also within a team. - Flexibility to meet project deadlines and goals; strong problem-solving ability highly desired. - Ability to adhere to strict confidentiality guidelines. - Ability to establish rapport with participants. - Ability to keep accurate and detailed records of all study procedures. - Experience with Microsoft Office products (Word, Excel, PowerPoint). - Confident and highly motivated with excellent multi-tasking ability and record-keeping skills. - Outstanding organizational skills with meticulous attention to detail. - Strong ability to work independently, exercising good judgement, with minimal supervision. - Demonstrated ability to learn and use new skills quickly and effectively. - Able to maintain data confidentiality and adhering to participant privacy. - Associate degree in Health Science or equivalent combination of related education and experience (necessary). - Minimum 1 year of directly related experience in clinical research and clinical trials (necessary). - OR advanced degree in a health-related area (Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD). - OR minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research. - High school diploma or GED is necessary (for Clinical Research Assistant? but seems alternative). Actually the text includes "Clinical Research Assistant High school diploma or GED is necessary." This seems like an alternative qualification for a different role? Might be part of required qualifications for this position? It says "Clinical Research Assistant High school diploma or GED is necessary." Might be a separate bullet for alternative path. We'll include as an option: High school diploma or GED. We'll list as bullet points. Desired Qualifications: after "Desired Qualifications*". The text: "Bachelor's degree in Health Science or an equivalent combination of related education and experience is desirable. An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable. experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable. Familiarity with OnCore, Epic, MiCHART, and eResearch applicationsKnowledge and experience with MyDataHelps, REDCap, Qualtrics, and other online databases.Community-engagement experience Ability to effectively communicate with staff and faculty of all levelsKnowledge of University policies and procedures" We need to deduplicate. Desired qualifications list: - Bachelor's degree in Health Science or equivalent combination of related education and experience. - Understanding of medical terminology. - Experience in a large complex health care setting. - Ability to effectively communicate with staff and faculty of all levels. - Knowledge of university policies and procedures. - Familiarity with OnCore, Epic, MiCHART, and eResearch applications. - Knowledge and experience with MyDataHelps, REDCap, Qualtrics, and other online databases. - Community-engagement experience. We'll list each as bullet. Benefits: from "What Benefits can you Look Forward to?": - Excellent medical