What are the responsibilities and job description for the Associate Director, Clinical Scientist/ Director, Clinical Scientist position at People With Chemistry?
Associate Director, Clinical Science (MD) / Director, Clinical Science (MD) Endocrinology
Meet is partnering with an innovative, fast-growing company specializing in metabolic and obesity therapies to identify exceptional candidates for the roles of Associate Director, Clinical Science (MD) and Director, Clinical Science (MD).
These critical positions will be instrumental in shaping and advancing the global clinical development strategy for affordable therapies in the endocrinology space.
Key Responsibilities
- Global Clinical Development Leadership :
Lead the global clinical development strategy, including study planning, medical dossier development (e.g., GIP, protocols, CSRs, COs, CS), and the startup, conduct, and monitoring of Phase I-IV clinical trials. Oversee the analysis and reporting of global and regional data (e.g., EU, US).
Partner with regulatory affairs teams to support interactions with health authorities during investigational new drug applications (pre-IND / IND), clinical trial permissions (CTPs), and new drug application (NDA) processes.
Collaborate with clinical operations staff to plan and execute global medical meetings, including investigator meetings, advisory boards, and other scientific forums with global investigators.
Provide strategic leadership and input across related medical functions, including biostatistics and clinical pharmacology.
Lead global data analysis efforts and contribute to the development of scientific publications (abstracts, posters, manuscripts). Serve as a speaker at scientific meetings to represent the organization.
Establish and maintain relationships with external scientific experts, thought leaders, and the broader medical community.
Qualifications
Medical Doctor (MD) with board eligibility or certification in Internal Medicine. A background in endocrinology is highly preferred.
Minimum of 3 years of experience as a clinical research physician in the pharmaceutical industry. Relevant experience will be considered for different levels of responsibility.
Strong understanding of the drug development process, with FDA / EMA experience preferred.
Willingness to travel domestically (US-based) and internationally as needed.
