Clinical Research Medical Director, Bone Health- California

Clinical Research Medical Director, Bone Health – California Tanner & Associates is recruiting a Clinical Research Medical Director in Bone Health for a large biotech company based in California. Please send CV to View email address on click.appcast.io Key Responsibilities Supporting the development, execution and communication of the global scientific/medical evidence plan Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program Supporting the development of key scientific external relationships with opinion leaders Participating and providing clinical input into safety and regulatory interactions Provide clinical/scientific input during the development and execution of clinical trials Interpret clinical trial data Participates in conducting safety assessments. Participates in interactions with regulatory agencies. Authors clinical study reports, publications and regulatory submissions Develops key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings Identify new clinical research opportunities Support in-licensing and out-licensing activities and partner relationships Support product lifecycle management for new indications Qualifications MD with 2 or more years of clinical research and/or basic science experience combined with clinical teaching and patient care activities, 5 or more years is preferred. MD plus accredited residency in Endocrinology, Rheumatology, Orthopedic Surgery, board certified or equivalent. Clinical research experience in the biopharmaceutical industry, biotechnology, and pharmaceutical Demonstrated ability to serve as a medical expert in a complex matrix environment. Medical/Scientific Knowledge In depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale. Familiar with basic concepts of clinical research and clinical trial design, including biostatistics. Knowledge of GCP, FDA and EMEA/CHP regulations and guidelines and applicable international regulatory requirements. #J-18808-Ljbffr TANNER & ASSOC INC