Role Description Join a paid research initiative in collaboration with a leading AI research organization focused on advancing healthcare operations, member experiences, and enterprise decision-making. We are seeking professionals currently working in large healthcare organizations to participate in a compensated online research survey. This study aims to better understand: - Operational workflows - Cross-functional collaboration - Technology adoption - Organizational challenges - Perspectives on emerging AI solutions within healthcare and health services environments Your insights will help inform the development of practical AI technologies designed to enhance efficiency, decision-making, and collaboration across healthcare enterprises. This is a fully remote, independent contractor opportunity involving a one-time online survey. Key Responsibilities - Complete a structured online survey lasting approximately 30 minutes. - Share insights from your day-to-day responsibilities and organizational workflows. - Provide feedback on operational processes, technology adoption, communication practices, analytics, customer or member experience, and strategic initiatives. - Discuss common challenges encountered within large healthcare organizations. - Offer perspectives on how AI-powered tools can improve efficiency, collaboration, and decision-making across healthcare functions. Qualifications - Currently employed by a large healthcare, health services, health insurance, pharmacy benefits, managed care, or related healthcare organization. - Currently working in one of the following functional areas: - Operations - Strategy - Product Management - Program Management - Sales - Account Management - Customer Experience - Marketing - Communications - Clinical or Pharmacy Leadership (non-patient-facing) - Information Technology - Engineering - Data & Analytics - Actuarial - Finance - Legal - Compliance - Experience working within enterprise healthcare or health services organizations. - Familiarity with organizational workflows, operational processes, and cross-functional collaboration. - Comfortable participating in structured research studies and providing thoughtful professional feedback. - Ability to independently complete an online survey. Engagement Details - Format: Online research survey - Duration: Approximately 30 minutes - Location: Remote (United States) - Compensation: Paid upon successful completion of the survey Why Participate - Contribute to the development of next-generation AI technologies for healthcare organizations. - Share professional insights that can improve healthcare operations and enterprise decision-making. - Help shape AI-powered tools designed to support healthcare professionals and organizational teams. - Participate remotely with a flexible, one-time time commitment. Equal Opportunity Statement We are committed to providing equal opportunities to all qualified participants without regard to legally protected characteristics. Reasonable accommodations are available upon request. Contract Information - Participation is offered as an independent contractor engagement. - The survey is completed remotely on your own schedule. - Compensation is issued upon successful completion of the survey. - Project opportunities may be extended or modified based on research requirements. - Participants will not be required to access or disclose confidential or proprietary information from any employer, client, or institution. - Please note that visa sponsorship is not available for this opportunity.

Title: Part-Time Clinical Research Coordinator Location: United States Job Description: APPLICATION INSTRUCTIONS: CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application process. Please do not apply here, apply internally through Workday. CURRENT PENN STATE STUDENT (not employed previously at the university) and seeking employment with Penn State, please login to Workday to complete the student application process. Please do not apply here, apply internally through Workday. * If you are NOT a current employee or student, please click "Apply" and complete the application process for external applicants. Approval of remote and hybrid work is not guaranteed regardless of work location. For additional information on remote work at Penn State, see Notice to Out of State Applicants. JOB DESCRIPTION AND POSITION REQUIREMENTS Dr. Kristina Petersen's lab in the Department of Nutritional Sciences is seeking a part-time Clinical Research Coordinator to support externally funded clinical trials investigating dietary interventions and risk factors for heart disease and diabetes. This role will involve study coordination for clinical trials being conducted in the lab. Tasks will include coordinating participant recruitment, conducting telephone and clinic screenings, coordinating data collection visits, visit scheduling, managing participant flow through the trials, and research-related administrative tasks. We are seeking a candidate that is reliable, proactive, task- orientated, attentive to detail, and has excellent communication, team-work, and organizational skills. Prior experience in humans subjects research is required, and prior experience in clinical trial coordination is highly desired. Training will be provided for the specific tasks this position requires. This position will involve approximately 20 hours per week of work with typical working hours being Monday to Friday 6:45 am to 10:45 am. This is an in-person job in State College, Pennsylvania. Applicants must submit a resume/CV and cover letter outlining their interest in the position, relevant prior experience, and availability for the position. BACKGROUND CHECKS/CLEARANCES This position requires the following clearances in addition to applicable background checks: PA State Police Criminal Background Check, PA Child Abuse History Clearance Form, and Federal (FBI) Fingerprint Criminal Background Check. CAMPUS SECURITY CRIME STATISTICS Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act and the Pennsylvania Act of 1988, Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters. The ASR is available for review here. EEO IS THE LAW Penn State is an equal opportunity employer and is committed to providing employment opportunities to all qualified applicants without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you are unable to use our online application process due to an impairment or disability, please contact 814-865-1473. Penn State is committed to and accountable for advancing equity, respect, and belonging. We embrace individual uniqueness, as well as a culture of belonging that supports equity initiatives, leverages the educational and institutional benefits of inclusion in society, and provides opportunities for engagement intended to help all members of the community thrive. We value belonging as a core strength and an essential element of the university's teaching, research, and service mission. Federal Contractors Labor Law Poster PA State Labor Law Poster Penn State Policies Copyright Information Hotlines

Title: Principal Biostatistician Job Description: Location: Home-based in the U.S. or Canada Why DSSS? Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies to market. Job Summary: The Principal Biostatistician is responsible for providing statistical support for pharmaceutical clinical trials in patients. Additional Benefits: - Home-based remote working opportunities. - Work/life balance as well as flexible schedules. - Collaborating with motivated, high-performance, statistical and research teams. - Technical training and tailored development curriculum. - Research opportunities that match your unique skillset. - Promising career trajectory. - Job stability: long-term engagements and re-deployment opportunities. - Focus on bringing new therapies to market rather than project budgets and change orders. - Experience with regulatory submissions. - Engaging, fast-paced environment. - Good work-life balance. Job Responsibilities: - Collaborate with multi-disciplinary project teams to establish project objectives and timelines. - Author statistical analysis plans. - Collaborate with Data Management, Clinical Development, and Clinical Operations with statistical expertise. - Author or review analysis dataset and TLF specifications - Validation programming of efficacy analysis datasets plus tables, listings, and figures (TLF) - Provide guidance and supervision to programmers in authoring analysis dataset specifications and programming/validation of tables, listings, and figures for safety, etc. - Interpret study results and review reports of study results for accuracy. - Support exploratory analyses. - Participate in IND or NDA activities. - Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. - Contribute to clinical study reports and other regulatory documents, e.g. NDA, DSURs, Briefing Documents, ISS, ISE, SCE (Summary of Clinical Efficacy), SCS (Summary of clinical Safety). Qualifications - PhD in Statistics, Biostatistics, or related field with 3+ years of industry experience. - MS in Statistics, Biostatistics, or related field with 5+ years of industry experience. - At least 2 years in Phase 2/3 clinical trial experience. - Demonstrated ability to work pro-actively and independently. - Able to effectively communicate ideas and collaborate with cross-functional teams - Ability to use R or SAS to perform efficacy and safety analyses and validate important data derivations when necessary. - Support of various regulatory submissions - Understanding of relevant FDA guidance, ICH GCP, ICH E9 plus general knowledge of industry practices and standards. - Experience in validation/programming of ADAM and TLF - Experience with CDISC, including SDTM, ADAM, CDASH - Solid understanding of estimands and multiple imputation methods. Desired Experience: - Supporting written communications with regulators. - 1+ years of experience with immunology therapeutic area. - Bayesian methods #LI-Remote

• This position reports to Manger/Sr. Manager, Medical Sciences and requires a strong candidate with expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies, and sound knowledge of applicable regulations and standards. • The position will mainly focus on the development of Clinical Evaluation Plans (CEPs) & Clinical Evaluation Reports (CERs), with a potential for future additional responsibility in the development of other clinical evidence documents. • The purpose of this job is to work collaboratively to develop strategies for the creation of CEPs followed by the development of clinical evaluation reports (CERs) per EU MDR, to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, re-certification and proposed indication/labeling changes. • Further, the responsibility includes the development of regular CEP and CER updates to maintain EU product conformance. • Interact with internal cross-functional teams (engineering, product development, regulatory, post-market surveillance) to define and plan the strategy for the development of CEPs and CERs for new products requiring CE Mark. • Develop and author clinical documentation for regulatory submissions, mainly key sections of the CEP, and the entire CER document. • Develop and author responses to the requests and questions on the clinical documentation from the regulatory authority. • Possess or acquire in-depth knowledge of therapeutic areas, competitor devices, current clinical/market developments, literature review processes and the ability to keep abreast of current literature. • 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; stay informed about applicable clinical landscapes and trends. • Provide product guidance and expertise to the clinical librarian to facilitate conducting literature searches on products/product families. • Review scientific literature and interpret and summarize published data on risks, alternate therapies and device-specific benefits; collect and summarize primary data to support risk assessment. • Critically appraise scientific literature and write clinical summaries for products and surgical procedures. • Conduct proofreading, editing, document formatting, review comment integration and document completion / approval activities. • Manage CEP/CER timelines required by product development teams and global Regulatory Bodies by utilizing appropriate project management tools. • Serve as the SME and/or functional representative for R&D development activities (e.g., Product or Technology Development Process teams) and support broader Clinical/Medical Affairs activities such as Regulatory submissions/responses. • Perform periodic reviews of risk documentation and product labeling; ensure appropriate updates are implemented. • Provide clinical perspective and support and guide new product development for CE Mark purposes. • May require participation in ongoing core team activities (e.g., weekly meetings) or provide periodic participation and input as needed. • Support the clinical affairs (CA) team with the creation of clinical content for other documents including Investigator brochures, manuscripts, scientific abstracts, conference presentations, and posters based on Intuitive clinical trials. • Support the CA team with the development and writing of clinical study protocols and Clinical Study Reports (CSRs). • Ensure compliance with corporate (e.g., SOP’s) and regulatory requirements (e.g., GCP and US and OUS guidelines)