Clinical Trial Nurse – Per Diem - Topsham, ME Work Set-Up: Local Travel – In-Home Patient Visits Job Type: Per Diem Are you a Registered Nurse looking for a flexible and rewarding opportunity in clinical research? Join IQVIA, a global leader in advancing healthcare, and make a real impact by supporting clinical trials in your community. We’re seeking experienced Registered Nurses to visit patients in their homes and assist with clinical trial activities that help bring innovative treatments to market. This role offers flexible scheduling (morning or early afternoon visits), making it ideal for PRN nurses or those working part-time who want to earn supplemental income while gaining exposure to clinical research. What You’ll Do - Conduct in-home visits with clinical trial patients. - Collect samples and data to evaluate the safety and efficacy of new medications. - You may perform tasks such as: - Drawing blood, taking vitals, and conducting urine tests. - Administering medication if required. - Labeling and shipping samples. - Visits with drug administration via subcutaneous injections. - Documenting adverse events and completing reports accurately and on time. - Review AEs (Adverse Events), SAEs (Serious Adverse Events), and conduct Mental Health (MH) reviews. Qualifications: - Active RN license in the state you work in - BLS certification required. - Recent experience with blood draws. - Comfortable using basic software programs. - Flexible availability and ability to travel regionally (up to 90 miles). - Reliable transportation, internet access, and a mobile phone. - Pediatric experience Why Join IQVIA? - Flexible schedule that fits your lifestyle. - Opportunity to travel locally and expand your professional experience. - Gain hands-on exposure to clinical trials and grow your career in research. - Competitive supplemental income. Ready to make a difference? Apply today and help shape the future of healthcare! Please note: This position is not eligible for sponsorship. #LI-CES #LI-DNP #LI-HCP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be 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, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $50.00-$60.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Research Scientist, Clinical Affairs Location: Remote United States Job Description: Research Scientist, Clinical Affairs Department: Medical Affairs Employment Type: Full Time Location: Remote Compensation: $100,000 - $125,000 / year Description At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne, you'll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage. The Research Scientist, Clinical Affairs plays a pivotal role in scientific design, execution and interpretation of research studies evaluating the safety, efficacy, and claims of dietary supplements. RESPONSIBILITIES Support the Director of Clinical Affairs to lead clinical and consumer research programs in support of new product offerings and differentiation of existing products. Scientific Rigor & Critical Thinking: - Design or meaningfully contribute to fit-for-purpose research protocols and methods including but not limited to in vitro, in vivo, and clinical and consumer studies, aligned with dietary supplement substantiation needs. - Develop and review protocols, informed consent forms, and related study documents; ensure research plans align with SOPs, regulatory/ethical guidelines (e.g., GCP, IRB requirements) and industry standards. - Independently synthesize literature and competitive information across multiple products and/or assigned therapeutic areas. Statistical Analysis & Data Interpretation: - Develop and review SAPs, ensuring they are scientifically sound. - Conduct statistical analysis of research data using appropriate statistical tools/programs. - Translate findings into clear conclusions and prepare technical reports, summaries and presentations without direct oversight. Cross-Functional & External Collaboration: - Partner effectively within R&D and facilitate seamless communication across teams to streamline internal decision-making. - Establish relationships and engage credibly with CROs and external experts to support scientific strategies and innovation. - Contribute to optimization of internal processes and workflows. - Develop new ideas for both external and internal projects. - Stay current with research methodologies, regulatory guidelines impacting dietary supplements, and scientific literature relevant to health outcomes measured in studies. - Provide operational or workflow support in management of research programs as needed. - Work collaboratively and contribute to other projects and functions of the greater Medical, Clinical, & Scientific Affairs team, as needed. WHAT YOU NEED - Master's or Bachelor's degree in Life Sciences, Nutrition, or related field with 8+ years of experience in consumer-packaged goods, dietary supplements, nutritional and/or functional foods. - Strong knowledge of scientific principles and clinical research methodology. - Proven experience in designing and managing human clinical trials and consumer studies. - Demonstrated ability to write and evaluate study methods and interpret data. - Excellent critical thinking, and scientific writing skills. - Strong understanding of GCP, ICH, FTC regulations and standards, IRB requirements and regulatory requirements for clinical trials of dietary supplements including FDA, DHSEA, and HIPAA regulations - Excellent organizational skills, strong attention to detail, and ability to manage multiple tasks concurrently. - Has broad knowledge of various technical alternatives and their potential impact on the business. WHAT WE OFFER - Competitive compensation - 100% company-paid medical, dental, and vision insurance coverage for employees - Company-paid short- and long-term disability insurance - Company- paid life insurance - 401k plan with employer matching contributions up to 4% - Gym membership reimbursement - Monthly allowance of Thorne supplements - Paid time off, volunteer time off and holiday leave - Training, professional development, and career growth opportunities #LI-SC1

Sr. Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: - Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. - Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. - Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. - Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. - Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: - Bachelor's degree in a relevant scientific discipline or healthcare-related field - Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. - Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. - Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. - Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. - Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Conduct site monitoring visits to assess compliance with protocols and regulations, review documentation for accuracy, and provide training to study staff, ensuring the protection of human subjects and data integrity throughout the clinical trial...