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Job Overview

Oversees the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy.

Key points

  1. Responsible for design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses…

  2. May oversee the work of Medical Directors and/or Scientific Directors, and of Clinical Scientists working on the same or related programs.

  3. Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area.

  4. Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as…

  5. Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment. Completion…

  6. Experience with psychedelic drug development highly preferred.

  7. Ability to run a clinical research program of moderate complexity with minimal supervision.

  8. Ability to perform and bring out the best in others on a cross-functional global team.

Languages

English required

Skills

CommunicationStakeholder Management

Experience: Senior-level · 2+ years · Job type: Full-time