Role Description The operational responsibilities as outlined below will be prioritized by the Project Manager, Clinical Research and the Senior Program Director of Clinical Research. - Essential Duties/Responsibilities (70%): - Project management - Assist in startup, feasibility and qualification of clinical trial services opportunity in collaboration with the business development team. - Scope workflow and understand deliverables from Statement of Work. - Execute all deliverables in collaboration with cross-functional leadership teams at Life Line Screening. - Prepare specs for all reporting needs necessary for all client and executive level project reports. - Deliver all reporting to client. - Demonstrate analytical ability business strategy, planning, and execution. - Essential Duties/Responsibilities (30%): - Client management, experience, and maintenance of industry knowledge. - Prepare and deliver all program reports and analyses. - Identify scope changes and provide timelines and process iteration for client understanding execute delivery within the agreed upon timeline. - Attend start up meetings remote and in-person when applicable. - Set regular agendas and lead project meetings with cross function operational teams. - Identify risk to project deliverables. - Manage day to day project operations for multiple clients at once. - Ancillary Responsibilities: - Develop processes and procedures for PM role within the expanding team. - Rapid response time to client needs and requests. - Coordinate IRB submissions and manage regulatory binders when applicable. - Prepare and deliver project-related training materials to team members. - Coordination with internal IT and external partners to ensure LLS has proper reports accessible for tracking patient activity through recruitment funnel as well as manage and maintain accurate reporting for invoicing of services. - Work with clinical trials team to manage and support process improvement plans to meet recruitment feasibility. - Reacts to and overcomes problems or objections from client. - Coordinates billing process. - Follows-up on all deadlines, making sure all materials, reports, invoices are on time. - Entertains and nurtures relationships with current and prospective clients. - Ability to travel ~10% nationally. - Work to establish plans to foster growth as routine gap analysis are conducted on the growing suite of services. Qualifications - BA/BS in the sciences, marketing, or business; or equivalent education/relevant experience. - Project Management Certification (such as PMP) is a plus. - 4+ years of project management experience in managing complex projects, in clinical research and clinical trial services. - Excellent time management. - Outstanding written and oral communication with attention to detail. - Proficient in Microsoft Office, Outlook, Excel, Word, PowerPoint and other related computer skills required. - Proficiency in Smartsheets is a plus. - Ability to maintain discretion and confidential information. - Strong organizational skills, time management skills and attention to detail required. - Ability to prioritize and manage multiple tasks/projects and support positions. - Ability to meet tight deadlines and work well under pressure. - Ability to work independently, be self-directed and demonstrate initiative. - Excellent ability to establish rapport with others and ability to build strong interpersonal relationships. - Exhibit good judgment and decision-making skills. - Must be a team player. - Proven team building and leadership skills. - Proven track record to gain confidence and maintain communication across all levels of the organization. Benefits - Life Line Screening is proud to be an equal opportunity employer. - Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status, or other characteristics protected by law. - Life Line Screening will only employ those who are legally authorized to work in the United States for this opening. - Any offer of employment is conditional upon the successful completion of a background check and drug screen. Company Description Privacy Notice to California Applicants

• This position reports to Manager/Sr. Manager, Medical Sciences and requires expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies • The position mainly focuses on the development of Clinical Evaluation Plans (CEPs) & Clinical Evaluation Reports (CERs) • Develop and author clinical documentation for regulatory submissions, mainly key sections of the CEP, and the entire CER document • Develop and author responses to requests and questions on the clinical documentation from the regulatory authority • Participate in and/or perform comprehensive literature searches to develop and maintain in-depth knowledge and understanding of current scientific literature required to support identified product lines and related clinical studies • Review scientific literature and interpret and summarize published data on risks, alternate therapies and device-specific benefits • Manage CEP/CER timelines required by product development teams and global Regulatory Bodies by utilizing appropriate project management tools

Role Description You are a talented Clinical Exercise Physiologist who will deliver care and support to our patients throughout our flagship virtual cardiac rehab program. You will play a defining role in the success of the groundbreaking clinical studies we are running with world leading health systems in Pennsylvania and New York. In this role, you will: - Be a part of our remote vitals monitoring clinical team. - Monitor, review, and assess daily patient vital readings (BP, HR, SpO2) and respond promptly to abnormal values with wellness check phone calls. - Report abnormal vitals readings to patient's care team via phone call or fax. - Support and encourage patient adherence and engagement in our vitals monitoring programs. - Complete all required clinical documentation and billing claims for vitals reports and patient encounters. - Collaborate closely with fellow CEPs across clinical teams to ensure patient safety and deliver high-quality care. - Partner directly with our founders to enhance and innovate our cutting-edge digital care delivery model. - Work alongside our technology team to create a seamless, supportive experience for patients and clients. - Show flexibility and a patient-first mindset, doing what it takes to ensure an engaging and effective rehab experience. - Take pride in delivering exceptional care to patients throughout their rehabilitation journey. - Empower patients by providing guidance and support, encouraging them to take ownership of their health and recovery. Qualifications - Bachelor's Degree in Exercise Physiology or equivalent (Master's preferred). - ACSM certification (preferred). - Minimum 1+ years of relevant clinical experience and top performance working as a Clinical Exercise Physiologist at an in-person Cardiopulmonary Rehab Facility. - Possess strong anatomy and physiology skills. - Above average proficiency working with mobile technology. - Great interpersonal skills that foster a caring environment for patients. - Diligence and organization with the ability to create and adhere to repeatable processes. - Ability to perform with little direction in a high-growth, early stage startup (ie self-driven). - Attention to detail. Requirements - Spanish language proficiency (bonus). - Experience working in clinical studies (bonus). - Remote work experience (bonus).

Role Description Make a Difference on Your Own Schedule and Terms! Hiring Per Diem Registered Dietitians for Virtual Visits! Can be located outside of Florida but must have an active Florida RD license. 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 Job Specific Details: - 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. 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 - No research experience required, on the job training provided - Gain Certification through GCP training Benefits - Standard Rate: $46.00 Hourly plus commute, mileage, training, and administrative pay. Company Description 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. 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.