Accomplished medical communications and medical affairs specialist with a strong background in managing
multifaceted projects within the healthcare sector. Over four years of experience in crafting compelling content and
overseeing safety and compliance in medical and promotional campaigns. I bring a deep understanding of diverse
health-related topics and the ability to make complex information easily understandable and relatable. Proficient in
collaborating with teams to drive projects to successful completion, and I am passionate about using my skills to
enhance overall communication strategies and improve outcomes. I am seeking opportunities to apply my expertise in
environments that value clear and impactful communication and innovative solutions

Lipscomb University

Conduct literature reviews, support data analysis, and develop peer-reviewed articles and slide presentations, ensuring accuracy, clarity, and compliance with regulatory standards and client messaging Work cross-functionally with teams and key opinion leaders, to manage multiple projects, ensuring timely delivery of client deliverables Develop internal educational slide kits, conference reports, and medical training materials to enhance the knowledge and skills of medical teams and stakeholders. Provide evidence-based scientific direction to account teams, clients, and other stakeholders, ensuring alignment with client brand strategy and adherence to compliance standards Conduct literature reviews, support data analysis, and develop peer-reviewed articles and slide presentations, ensuring accuracy, clarity, and compliance with regulatory standards and client messaging Work cross-functionally with teams and key opinion leaders, to manage multiple projects, ensuring timely delivery of client deliverables Develop internal educational slide kits, conference reports, and medical training materials to enhance the knowledge and skills of medical teams and stakeholders. Provide evidence-based scientific direction to account teams, clients, and other stakeholders, ensuring alignment with client brand strategy and adherence to compliance standards

Senior Medical Writer | Medical Communications

Effectively leveraged scientific expertise across various projects on client teams, to drive growth of existing accounts and onboarding of new accounts Authored peer-reviewed articles in medical journals, advancing academic knowledge and integrating latest research into medical education Designed and delivered educational materials and electronic-learning modules for medical students, focusing on oncology and immunology, to enhance academic and clinical understanding Supported marketing and medical teams by supplying vital information about products and therapies, aiding in the development of strategic plans for effective communications Provided evidence-based scientific direction to account teams, clients, and other stakeholders, ensuring alignment with client brand strategy and adherence to compliance standards

Medical Communications Consultant

Authored original content, including manuscripts, white papers, peer-reviewed articles, feature articles, how-to guides, infographics, and storyboard explainer videos for healthcare professionals and patients Developed web content to support client marketing initiatives, ensuring brand consistency and compliance with standards Conducted literature reviews across oncology, immunology, and psychiatry, identifying knowledge gaps and formulating research proposals for continuing medical education (CME) initiatives Provided evidence-based scientific direction to account teams, clients, and other stakeholders, ensuring alignment with client brand strategy and adherence to compliance standards Collaborated with key opinion leaders (KOLs) and client medical strategy teams to manage and deliver projects from kick-off to completion Developed and updated workshop slide decks with clinical data readouts from American Society of Clinical Oncology (ASCO) and Psych Congress abstracts and posters, covering multiple therapeutic areas, including oncology and psychiatric disorders Contributed to the development of market access strategic payer council slide decks for various clients Crafted high-quality topline summaries (TLS) from workshops in various therapeutic areas, synthesizing key findings for strategic decision-making Created disease state expertise slides for internal training and client pitch presentations Provided medical information to client teams, supporting strategic initiatives and aligning with client objectives

Contributed to clinical study reports across multiple therapeutic areas, including oncology and infectious diseases, ensuring regulatory compliance for Food Drug Administration (FDA) submissions Authored sections of clinical study documents, including informed consent forms, enrollment flyers, and investigator’s brochures (introduction, summary of data and guidance for investigator, drug product information) Monitored clinical trials for compliance with study protocols, regulatory requirements, and GCP guidelines Coordinated with investigators and site staff to ensure timely and accurate data collection and reporting Assisted in the development and delivery of comprehensive training materials to support regulatory compliance Collaborated with the clinical trial manager (CTM) and regulatory teams to develop strategies for successful study completion and approval

Medical Writer | Medical Affairs | Clinical Research

ICON, Full-time, Remote Monitored and captured Individual Case Safety Reports (ICSRs) using Spotfire and Argus, ensuring accurate and timely adverse event data for patient safety and regulatory compliance Utilized Argus Safety database for entry, processing, and reporting of adverse events in accordance with E2B and regulatory guidelines Authored comprehensive summary narratives of ICSRs in Argus, ensuring accurate documentation for regulatory submissions Contributed to the development and delivery of safety training materials to internal teams and external stakeholders, enhancing understanding of pharmacovigilance processes Assisted in preparing Development Safety Update Reports (DSURs) for regulatory submissions Collaborated with cross-functional teams to ensure timely and accurate adverse event reporting to regulatory entities, including the FDA and European Medicines Agency (EMA)

Samuel Amadi

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