Role Description Make a Difference on Your Own Schedule and Terms! Hiring Per Diem Bilingual Registered Dietitians for Virtual Visits! Must be fluent in Spanish/English. EmVenio Research provides quality, in-home clinical trial visits for various Sponsors and CROs. We're the only company that hires, trains, certifies, tests, and manages our own Registered Dietitians. Our mission is to bring clinical trial visits to subjects wherever they may be to increase convenience and compliance with study protocols. Be part of a team who fully embrace our values and key behaviors! - We work as a team - We do the right thing - We figure it out - We pursue growth - We take ownership Why work for EmVenio? - We bring research to every neighborhood — making it more accessible, more inclusive, and more human — so every community can share in the promise of better care. - Be a member of our general staffing pool - No research experience required, on the job training provided - Gain Certification through GCP training Qualifications - Bachelor’s degree from an accredited dietetics program (If CDR examination was before January 1, 2024) - Graduate degree from an accredited dietetics program (If CDR examination was on or after January 1, 2024) - Registered Dietitian (RD) or Registered Dietitian Nutritionist (RDN) Certification by the Commission on Dietetic Registration (CDR) - Current State Dietitian License/Certification in good standing (if applicable) Requirements - Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant’s goals and values. - Sets appointments with subjects within the required appointment window. - Completes virtual visits for clinical trial subjects. - Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner. - Regularly stay informed on the latest nutrition and food health updates. - Performs additional duties and responsibilities as deemed necessary. Benefits - Standard Rate: $46.00 Hourly plus commute, mileage, training, and administrative pay. Contact Information Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career! Professional Case Management is an Equal Opportunity Employer.

Role Description Provide advanced biostatistical services for investigators, including: - Data preparation - Analyses - Methods and design consultation - Writing of statistical results Conduct analytical work leveraging advanced statistical methodologies such as: - Survival analysis - Longitudinal analysis - Mixed models - Regression analysis - Causal inference Collaborate with interdisciplinary teams to: - Translate data into actionable strategies - Work on multiple clinical research projects - Integrate data analysis from multiple organizations Develop predictive models to: - Refine risk assessment - Optimize protocols based on research insights Contribute to: - Peer-reviewed publications - Conference presentations - Communicate findings to diverse audiences, including clinicians, scientists, and programmers Qualifications - Bachelor’s degree in Biostatistics or a closely related field and 3 years of related experience - Alternatively, a Master’s degree in the same field and 1 year of related experience Requirements - Experience performing advanced statistical programming in a healthcare environment using SAS and R - Statistical methods including mixed modeling, propensity score matching, inverse probability treatment weighting, and survival analysis - Experience performing clinical trial analytics - Working with large and complex datasets such as PHTS, PEDIMACS, and SVR trial - Telecommuters considered Benefits - Salary Range: $98,820.00 to $153,170.00 - Commitment to fair and transparent pay practices - Factors such as skills and experience could result in an offer above the salary range noted in this job posting

Role Description This position is based in Park Ridge, IL, but the director may work remotely. Some travel (2-5X/yr) is required to meet with leadership and teams. Occasional work at night and weekends may be needed for special projects/events. - Oversees, develops, monitors, directs and advances clinical trial initiatives and operations necessary to achieve AAH and Advocate Aurora Research Institute (AARI) goals and priorities. - Works closely with the Medical Research Director(s) to cultivate, support, and enhance collaborative relationships with clinician investigators and industry and government sponsors, and to oversee individual protocol review, selection and performance. - Has direct authority for clinical trials operations teams consisting of manager(s), and individual contributors responsible for the conduct of clinical trials research, and for areas that support research excellence and compliance, such as quality, regulatory and education. - Establishes effective, efficient, high quality and valued research activities through quantifiable and standard metrics and develops mechanisms to drive measurable performance improvement. - Directs, promotes and supports high integrity, safe, compliant and cost-effective clinical trials operations. - Develops and enhances capabilities, reputation, visibility, awareness and competitive edge of research at AAH. - Leads by example in creating a culture of teamwork, engagement, diversity, equity and inclusion. - Performs human resources responsibilities for staff which include interviewing and selection of new team members, promotions, staff development, performance evaluations, compensation changes, resolution of team member concerns, corrective actions, terminations, and overall morale. - Works with senior leadership to develop and recommend operating and capital budgets. Provides financial management and controls expenditures within approved budget objectives. - Supports investigator development by guiding new and established investigators through the clinical trials process. - Accountable for developing strategy for and managing or leading appropriate committees and councils within his/her area(s) of research responsibility. - Accountable for adherence to quality standards, applicable laws and regulations, protocol requirements and federal guidelines pertaining to clinical trial research. - Oversees the quality monitoring program for all clinical trial research. - Responsible for understanding and adhering to the organization's Code of Ethical Conduct and for ensuring that personal actions, and the actions of employees supervised, comply with the policies, regulations and laws applicable to the organization's business. Qualifications - Master's Degree in Health Science or related field, or Master's Degree in Life Science. - Typically requires 7 years of experience in clinical research. - Typically requires 3 years of management experience in increasingly responsible administrative experience, with evidence of leading and managing clinical research programs and staff, educational activities, and special projects. Requirements - Proven experience leading successful clinical research program(s) with measurable success. - Manage concurrent complex projects, resources & deadlines. - Experience developing/implementing group processes, procedures and collaborations. - Demonstrates leadership to ensure high quality, ethical and compliant research and educational conduct. - Expert understanding of the conduct of clinical and/or translational research including oversight of human subject research, clinical trials, FDA Regulations, regulatory compliance, and good clinical practices (GCP) principles in research. - Possesses knowledge of grant/contract application/award processes, regulations and regulatory process required to conduct human subject research. - Is current on relevant literature in health services and clinical research. - Understanding of healthcare data, processes, workflows, and clinical research environments. - Strong analytical and organizational skills. - Ability to work in a complex corporate environment. - Excellent communication, problem solving and conflict resolution skills. - Ability to communicate effectively at all levels of an organization. - Ability to develop and maintain positive, productive working relationships with employees, donors, physicians, corporate leaders, civic/community leaders and other professionals. Benefits - Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training. - Premium pay such as shift, on call, and more based on a teammate's job. - Incentive pay for select positions. - Opportunity for annual increases based on performance. - Paid Time Off programs. - Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability. - Flexible Spending Accounts for eligible health care and dependent care expenses. - Family benefits such as adoption assistance and paid parental leave. - Defined contribution retirement plans with employer match and other financial wellness programs. - Educational Assistance Program.

Role Description The Clinical Research Associate (CRA) is responsible for set-up, initiation, execution, monitoring, and close-out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The CRA should be able to solve problems and analyze possible solutions using technical experience and judgement, while receiving a moderate level of guidance and direction. This position reports to the Manager, Clinical Site Operations and is part of the Global Clinical Affairs organization. The position will be fully remote within the United States. In this role, you will have the opportunity to: - Oversee clinical study protocol execution at external sites, from start-up to close-out, ensuring timely data collection and compliance with FDA standards and Good Clinical Practice (GCP). - Develop and maintain relationships with institutions, study investigators, internal stakeholders, and vendors to ensure successful trial execution, data integrity, and adherence to project requirements. - Conduct study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse events. - Manage IRB submissions and all study regulatory documentation. - Contribute to study planning including budget and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc. Qualifications - Bachelor’s degree with 2+ years clinical research experience OR Master’s degree with 0-2 years clinical research experience. - Basic knowledge of regulatory requirements and Good Clinical Practice for in vitro diagnostic and medical device products. - Previous experience with managing clinical research sites and monitoring clinical study data. - Good technical background to understand and communicate current and new technologies. - Ability to work on multiple projects simultaneously. Requirements - Ability to travel 20-70%– including overnight(s), within the US. Travel may be up to 70% during project initiation periods. Benefits - Comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees. - Flexible, remote working arrangements for eligible roles. - Annual salary range of $85,000 - $95,000. - Eligible for bonus/incentive pay.