Title: Research Associate Location: Ann Arbor United States Job Description: Employment Type: Part time Shift: Day Shift Description: Department: Academic Research Project Location: Trinity Health Ann Arbor Minimum Rate: $19.45 Total Rewards and Benefits: - Competitive compensation, DAILYPAY - Benefits effective Day One! No waiting periods. - Full benefits package including Medical, Dental, Vision, PTO, Life Insurance, Short and Long-term Disability - Retirement savings plan with employer match and contributions - Opportunity for growth and advancement throughout Trinity Health - Tuition Reimbursement Position Purpose: Assists in coordinating day-to-day activities associated with clinical research study independently and under the direction of senior research staff and principal investigators to ensure that the objectives of an established research protocol are met and in compliance within IRB and sponsor guidelines. Identifies and recruits' patients into study protocols. Will interface with research participants to recruit, assess eligibility criteria, determine subject availability, assist investigators with obtaining informed consent, perform follow up data collection and enter into the database. This is a State of Michigan sponsored study looking to recruit eligible participants who present to an outpatient clinical setting for obstetrical care. This position is term-limited and contingent upon grant funding continuation and successful patient recruitment. May require driving between Trinity OB clinics. Shift Available: Days Status Available: Part-time Required Qualifications: Education - Bachelor's degree in a related science, healthcare or business field or the equivalent combination of education and experience. Experience - One year of related research experience preferred. - Familiarity with the principles of obtaining informed consent preferred. - Knowledge of basic research design principles, statistics, regulatory and ethical requirements preferred. - Knowledge of medical terminology preferred. - Excellent writing and interpersonal communication skills. - Working knowledge of database systems and good basic computer skills. Physical and Mental Requirements and Working Conditions: - Normal office environment, outpatient setting. - Professional, calm, and compassionate demeanor in the presence of injured and stressed patients and families. - Ability to work some flexible hours to accommodate study and patient schedules is required. - Ability to work independently and with high accountability, and ability to work in team settings. What you will do: - Monitor obstetrical clinic schedules to screen for potential participants. - Review the medical record to assess eligibility based on defined criteria. - Recruit patients and obtain informed consent to Mission and Department standards. Consenting process includes the ability to do phone calls, e-consent, or in-person. - Conduct research surveys and other protocol activities. - Enter, clean, and manage research data. - Organize study supplies and request inventory as needed. - Reviews the accuracy, completeness, and timeliness of completed study related records, case report forms, and other documents. - Learn and adhere to clinic visitor, infection control, contact policies and appropriate provider communication. - Communicate questions and findings in a timely manner to the appropriate parties beginning with the Research Coordinator and possibly including but not limited to research administration, principal investigators, and compliance staff. - Assist in the preparation of IRB reports and submissions. - Assist with non-invasive study procedures with prior IRB approval (minimal risk studies only) upon completion of orientation requirements under direct supervision of a Research Coordinator. - Perform clerical duties, schedule meetings. - Performs related responsibilities, and special projects as required. Our Commitment Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.

Clinical Research Associate Location: Madison United States Job Description: Piper Companies is actively seeking Clinical Research Associates to join a highly accredited CRO. This position is fully remote but does require travel 60-80% of the time regionally with the Midwest region. The Clinical Research Associate will take part in a very essential role in assisting the process of creating lifesaving drugs and treatments. Responsibilities of the Clinical Research Associate: - Oversee the development and execution of the clinical trial plans and protocols for Phase I-IV - Maintain documentation and data evaluations - Work collaboratively with the team to ensure monitoring activities meet study requirements - Conduct on site field evaluations Qualifications of the Clinical Research Associate: - Experience with Oncology as a therapeutic indication - 3+ years of clinical monitoring experience, specifically with Oncology - Experience with the FDA or similar Regulatory and Accrediting administrations - Bachelor's degree in one of the life sciences or related background Compensation for the Clinical Research Associate: - Salary Range: $120,000-$135,000 - Comprehensive Benefits: Medical, Dental, Vision, 401k, and sick leave if required by law This job opens for applications on 1/20. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: Clinical Research Associate, CRA, BA, life sciences, clinical trials, phases, documentation, data, monitor, study, onsite, FDA, drugs, treatments, medical, dental, vision, 401k #LI-KI1 #LI-HYBRID

• The Research Analyst will report to the Manager of Global Evidence Management team and will play a key role in executing scientific research projects focused on evidence synthesis, meta-analysis, and real-world evidence. • Conduct high-quality systematic literature reviews, meta-analyses, and outcomes research. • Collaborate with broader Global Access, Value and Economics, Market Access and Customers Analytics, Clinical and Regulatory Affairs. • Execute systematic literature reviews according to PRISMA methods and Cochrane guidelines. • Perform meta-analyses using statistical analysis tools such as R software. • Conduct real-world evidence studies and collaborate with cross-functional teams to translate research findings into actionable insights. • Present data and findings clearly and effectively to internal and external stakeholders. • Prepare scientific manuscripts, abstracts, posters, and presentations for peer-reviewed journals and conferences, ensuring compliance with relevant publication standards.

• Research plot maintenance and preparation- Preparing sites to include planting, maintaining, spraying and harvesting the research plots. • Prepare for training sessions or grower field days. • Grooming plots and planning protocol execution to coincide with these events is paramount. • Crop scouting/advising - Walk research plots to evaluate weed control, insect infestations and disease outbreaks, consulting with Agronomists or Technical Seed Managers on solutions, and planning operations to resolve issues with crop production. • Help train and guide summer interns to complete operational goals. • The Research Specialist develops workflows, task lists and trains summer interns on skills necessary to complete the work in a timely manner with exceptional quality. • Planning Activities – Assist research manager with planning and organizing the following: sourcing research sites, developing contracts, site layout, entry lists, database setup, equipment prep, fertilizer and crop protection planning, operational plans, and data flow planning. • Work with Land O’Lakes safety team to ensure DOT and Safety compliance. This includes tracking fuel receipts, RAIR compliance; ensuring proper logbook procedures are followed.