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TANNER & ASSOC INC

Clinical Research Medical Director, Bone Health– California

TANNER & ASSOC INC, Los Angeles, California, United States,


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 careers@biotechserach.com.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.Providing clinical/scientific input during the development and execution of clinical trials.Interpreting clinical trial data.Participating in conducting safety assessments.Participating in interactions with regulatory agencies.Authoring clinical study reports, publications and regulatory submissions.Developing key opinion leaders and making scientific presentations at advisory boards, key scientific meetings, and external committee meetings.Identifying new clinical research opportunities.Supporting in-licensing and out-licensing activities and partner relationships.Supporting 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 sectors.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.Familiarity 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.

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