Associate Director - Medical Information - Hybrid

Our client, a global leader in biotechnology, is seeking a highly motivated "Associate Director - Medical Information" to join its Antiviral Research team for Foster City/Santa Monica/ Parsipanny/Rayleigh. Duration: Long term contract (Possibility of further extension) Pay Rate: $90 - 100/Hr on W2 + Medical Benefits, Paid Sick leave, 401K We are seeking an experienced Medical Information professional to provide scientific and operational support for Medical Information activities. The role will focus on responding to medical inquiries, developing scientific response materials, and supporting launch readiness for an upcoming multiple myeloma product launch. Key Responsibilities Respond to unsolicited medical inquiries from healthcare professionals, patients, caregivers, and internal stakeholders with accurate, evidence-based information. Manage complex medical inquiries and develop scientific response materials, including Standard Response Letters (SRLs), FAQs, and Q&A documents. Review clinical data and scientific literature, translating complex findings into clear, balanced communications. Support product launch readiness, label updates, scientific congresses, and new data disclosures. Collaborate with Medical Affairs, Clinical Development, Regulatory, Patient Safety, Quality, and other cross-functional teams. Analyze inquiry trends, identify content gaps, and update response materials based on emerging evidence. Oversee vendor deliverables, provide scientific training, and ensure compliance with applicable safety and regulatory requirements. Maintain accurate documentation and report adverse events and product complaints according to established procedures. Required Qualifications Advanced scientific or medical degree (MD, PhD, PharmD, or equivalent). Ideally, 5+ years of Medical Information experience in the pharmaceutical or biopharmaceutical industry. Experience managing complex medical inquiries and developing scientific response content. Strong scientific literature review, clinical data interpretation, and medical writing skills. Knowledge of pharmaceutical regulations, safety reporting, fair balance, and compliance requirements. Excellent communication, project management, and cross-functional collaboration skills. Preferred Qualifications Experience in hematology/oncology, immuno-oncology, or cell therapy. Knowledge of multiple myeloma and product launch readiness. Experience with Medical Information vendors, content management systems, CRM platforms, or inquiry trend analysis. Please respond with your updated resume & contact information to hr@dawarconsulting.com/kavitha@dawarconsulting.com Best Regards, DAWAR CONSULTING INC.