Associate Director, Medical Affairs - # 26-15505

$120 per hour Cambridge, MA Contract Duration: 5 Months contract Schedule: Hybrid preferred; remote candidates will also be considered. If hybrid, candidate is expected to visit the office at least twice per week (days based on business need). High likelihood of extension beyond the current end date. Summary & Purpose of the Position Reporting to the Senior Director, Medical Affairs (Adult Cholestatic Diseases) , the Associate Director, Medical Affairs will support and oversee select medical affairs activities related to biliary atresia . This role will contribute to the U.S. medical strategy for elafibranor and the broader Medical Affairs plan for cholestatic diseases. Responsibilities Medical review of non‑promotional and promotional content. Information responses (in collaboration with Medical Information). Scientific communications including poster presentations and publications (in conjunction with the Publication/Medical Communications team). Advisory board planning. Design and medical monitoring of U.S.-based clinical studies. Review and approval of educational grants. Partnering with the MSL team to develop and manage regional relationships with Thought Leaders (TLs). Assessing Investigator‑Sponsored Study (ISS) requests in collaboration with local and global Medical teams. Working closely with the Global Training & Capabilities Excellence team to provide relevant internal training. Collaborating with U.S. and Global Medical Information teams to ensure Medical Information Response documents are accurate. Key Internal Partners Medical Affairs (all sub‑functions) Commercial Team Global Medical Cholestatic Disease Personnel Main Responsibilities & Technical Competencies Contribute to developing and implementing medical strategies aligned with organizational goals and objectives. Serve as Subject Matter Expert (SME) on medical and/or disease area and asset cross-functional committees, as appropriate. Support clinical research projects, including design, execution, and analysis of clinical trials. Develop content for external medical education programs and lead presentations where applicable. Contribute to and lead advisory board planning and execution activities. Train internal Medical and cross‑functional partners on disease area and product content as an SME. Review and approve promotional and medical materials through PRC and MRC, respectively. Provide medical input and oversee budgets for clinical grants and medical education support activities in coordination with the Grants Manager. In collaboration with the Medical Communications Director, lead development of high‑quality scientific and educational materials, including MSL slide decks, FAQs, medical fact sheets, advisory board content. Contribute to the U.S. scientific publication plan. Attend relevant congresses to participate in scientific exchange and provide congress coverage. Support planning, execution, and budget oversight of medical activities for cholestatic diseases. Demonstrate excellent verbal and written communication skills to effectively communicate complex medical information. Apply strong project management skills to oversee multiple projects and ensure timely completion. Behavioral Competencies Required Communicates Effectively Asks open questions and explores different perspectives with care and respect. Communicates transparently while remaining respectful. Delivers clear, structured, and focused messages using visual communication and storytelling. Demonstrates gravitas. Business Insights Makes decisions based on data, facts, and patient perspectives. Translates insights into objectives and sets high standards. Collaborates Collaborates across functions without organizational boundaries. Continuously removes barriers and drives continuous improvement. Demonstrates resourcefulness, learning mindset, and entrepreneurial behavior. Manage Complexity Identifies contradictory information and solves complex problems. Develops and evaluates alternative solutions. Prioritizes effectively to drive meaningful decisions. Ensures Accountability Defines clear ownership for tasks and projects. Promotes accountability and clarification of responsibilities. Consults appropriate stakeholders before making decisions. Takes ownership of decisions, actions, successes, and failures. Ensures commitments are completed. Knowledge & Experience (Essential) 5+ years of pharmaceutical industry experience, primarily within Medical Affairs. Additional exposure to clinical trials and/or research is a plus. Ability to effectively interact with cross‑functional teams. Knowledge & Experience (Preferred) Experience in Rare Disease or Liver/GI. Experience launching a new product or indication. Experience presenting and publishing scientific information. Education / Certifications (Essential) Advanced scientific degree required. Preferred degrees: MD, DO, PhD, PharmD. US Tech Solutions is 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, or status as a protected veteran. #J-18808-Ljbffr US Tech Solutions