About Advanced Medical Strategies AMS is the premiere provider of payment integrity, risk management, and business intelligence solutions that drive smarter, faster, more cost-effective care. Payment Integrity Explore cutting-edge solutions that empower your team to automate payment integrity processes, avoid or recover overpayments, and reduce outsourcing costs. Risk Management Enhance critical coverage decisions with analytical tools that support >90% of all stop-loss and reinsurance premiums written annually. Business Intelligence Strengthen your contracts and policies with powerful predictive analytics, advanced reporting tools, and consultative support. Position Overview We are seeking a detail-oriented and self-motivated Research Assistant to join our team. This role involves conducting in-depth research using reputable medical resources to support our drug and diagnosis directories. The ideal candidate will be comfortable analyzing complex clinical data, interpreting medical literature, and presenting findings clearly and professionally to both internal teams and clients. This role is 100% remote. Duties and Responsibilities Conduct and compile research on: · Survival and relapse rates · Treatment and drug efficacy data · Cell and gene therapy outcomes · Transplant success rates and related metrics · Additional clinical data as requested by the clinical team Analyze, interpret, and effectively communicate research findings · Utilize credible sources, including peer-reviewed medical journals, clinical studies, and subscription-based databases · Ensure accuracy, consistency, and clarity in all published and internal materials · Work independently while managing deadlines and maintaining high-quality standards · Prepare and write monthly client newsletters · Assist in developing engaging, educational social media content Skills and Qualifications · Bachelor’s degree in Life Sciences, Public Health, Medical Research, or a related field (or equivalent experience) · Strong analytical and research skills with exceptional attention to detail · Ability to read and interpret complex medical and scientific literature · Excellent written communication skills, including experience creating client-facing content · Ability to manage multiple projects and work independently in a deadline-driven environment · Familiarity with medical terminology and statistical concepts · Proficiency in Microsoft Office Suite and research tools/databases · Understanding of data confidentiality and compliance standards in healthcare · Experience with social media content creation is a plus Suggested Pay Range - $60,000 - $70,000 commensurate with experience and education The above statements are intended to describe the general nature and level of work being performed and are not intended as an exhaustive list of all responsibilities, duties, and skills required of the position. Nothing in this document is intended to exclude the opportunity for modifications or adjustment to the job or the manner of performing it consistent with the requirement to provide reasonable accommodations to the disabled. With or without accommodation, the essential functions must be performed. Employees unable to accomplish any functions may request reasonable accommodations pursuant to the Americans with Disability Act.

Title: Safety Scientist II/ III, EMEA - Remote, Serbia - Remote, Romania - Remote, Czechia - Remote, Bulgaria - Remote, Hungary - South Africa - Remote, Portugal - Remote, Poland - Remote, Spain - Remote, Croatia Full time Remote Responsible for the planning, coordination and delivery of signal detection and product safety scientist activities, with a focus on tasks which are low to high in complexity or which concern low to high complexity products. Additionally supports mentoring of more junior colleagues, development of processes/tools/systems, and may serve as lead on smaller FSP-type projects. Essential Functions: - Serves as a creator/contributor for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products. - Serves as a creator/contributor for signal detection and product safety scientist tasks which are ultra-high in complexity, or which concern ultra-high complexity products, under supervision by a more experienced team member. - Conducts quality review for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products. - Advises clients on safety related issues under supervision by a more experienced team member. - Leads small FSP projects. - Supports training and mentoring of junior colleagues. - Contributes to development of processes, tools and systems. - Participates in bid defence and proposal development activities. - Works within multiple company and client systems. Interacts with project team members and clients. - Ensures that tasks are conducted in accordance with company policies and procedures, contractual agreements, and applicable regulations. - Participates in departmental initiatives; Serves as a subject matter expert in designated area. - Responsible for routine project implementation and coordination for assigned projects, including leading kick-off meetings, coordination of communications and data requests, participation in client meetings, audits and inspections, and review of metrics and budgets. - Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors. - Having wide-ranging experience, uses professional concepts and company objectives to resolve complex issues in creative and effective ways. - Determines methods and procedures on new assignments and may coordinate activities of other personnel (i.e., Team Lead). Exercises' judgment in selecting methods, techniques and evaluation criteria for obtaining results. - Frequent contacts with internal personnel and outside customer representatives. Keys to Success: Education and Experience: Bachelor's degree Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years). Knowledge, Skills and Abilities: - Expertise in pharmacovigilance requirements relating to marketed products and clinical trials across all major markets - Excellent attention to detail, data interpretation and medical-scientific writing skills - Advanced critical thinking and problem-solving skills with ability to evaluate and escalate appropriately Solid project management skills with the ability to manage multiple projects simultaneously and ability to redress issues proactively with limited management intervention - Ability to motivate, mentor and provide guidance to less experienced staff, routinely exhibiting robust and proactive scientific expertise - Proficient at complex project administration including budget activities and forecasting - Excellent oral and written English language communication skills, including paraphrasing skills - Advanced computer skills with the ability to work within multiple systems; advanced skills in Microsoft Office products (including Outlook, Word, and Excel) - Ability to maintain a positive and professional demeanor in challenging circumstances and to proactively plan for likely scenarios using personal experience - Ability to work effectively within a team to attain a shared goal

Title: Field Applications Scientist, Proteomics (Remote - MD/DC) Location: Wilmington Delaware United States of America Remote Full time As a Field Applications Scientist, you will provide technical support and training for our Olink proteomics product portfolio. You'll serve as a scientific advisor, helping customers optimize their workflows and maximize the value of their investments while contributing to our mission of making the world healthier, cleaner, and safer. Location: This is a remote role based in the DC area. Please note that relocation assistance is not provided for this position. A Day in the Life: - Provide technical support and training for the Olink proteomics product portfolio - Collaborate with sales teams and customers to deliver product demonstrations and applications support and training that enables research and innovation - Deliver both pre- and post-sales technical expertise across multiple technology platforms - Develop new applications and troubleshoot complex technical issues - Build and maintain strong relationships with customers and internal stakeholders - Partner cross-functionally with sales, marketing, R&D, and product management teams to ensure customer success and drive business growth through technical excellence. Keys to Success: Education - Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, or related field with 5+ years of relevant experience; Advanced degree with 3+ years of relevant experience Experience, Knowledge, Skills, Abilities - Demonstrated expertise in method development and technical problem-solving - Clear written and verbal communication skills with ability to explain complex concepts to diverse audiences - Strong presentation and training capabilities for both technical and non-technical audiences - Ability to work independently and collaboratively in a results-oriented environment - Experience in project management and ability to handle multiple priorities - Customer service orientation and interpersonal skills - Ability to build and maintain effective relationships with internal teams and external customers - Willingness to travel up to 25-50% Other: - Must be legally authorized to work in the United States without sponsorship now or in the future - Must be able to pass a comprehensive background check and drug screen Compensation and Benefits The salary range estimated for this position based in District of Columbia is $83,300.00–$125,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: - A choice of national medical and dental plans, and a national vision plan, including health incentive programs - Employee assistance and family support programs, including commuter benefits and tuition reimbursement - At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy - Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan - Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

Home based position 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 We are currently seeking a Regulatory Scientist to join our diverse and dynamic team. As a Regulatory Scientist at ICON, you will support the development, implementation, and execution of regulatory strategies for clinical development programmes in Canada. You will contribute scientific and regulatory expertise to ensure submissions meet global requirements and support successful product development. What You Will Be Doing: - Contributing to regulatory strategy development for clinical programmes, including plans for health authority and central ethics interactions and submissions. - Preparing, reviewing, and coordinating regulatory documents such as clinical trial applications, briefing packages, and responses to health authority and central ethics questions. - Ensure deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures within contractual timelines and budget with sound scientific/technical principles. - Track and file central submission/approval progress in Clinical Trials Management System (CTMS), eTMF and other applicable systems ensuring accuracy and completeness of data/documents entered - Collaborating with clinical, safety, CMC, and other cross-functional teams to ensure alignment of regulatory content and messaging. - Monitoring changes in the regulatory environment and providing guidance on potential impact to programmes and submissions. - Supporting regulatory interactions and meetings, including preparation of materials and documentation of outcomes. Your Profile: - Degree in life sciences, pharmacy, or a related field, or equivalent scientific and regulatory experience. - Experience in regulatory affairs, regulatory writing, or clinical development within the pharma, biotech, or CRO industry. - Good understanding of global regulatory frameworks and guidelines relevant to clinical development. - Strong scientific, analytical, and critical thinking skills, with the ability to interpret complex data and regulations. - Excellent written and verbal communication skills, with high attention to detail and accuracy. - Ability to work effectively in cross-functional teams and manage multiple regulatory activities and timelines. - Read, write and speak fluent English 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