CSG
Medical Director - Endocrinology (Obesity)
CSG, Redwood City, California, United States, 94061
Medical Director - Endocrinology (Obesity)
Location:
United States (Remote)
A growing biotech with an expanding late-phase pipeline is seeking an
experienced Medical Director
to lead clinical development efforts in endocrinology, with a focus on obesity. This is a high-impact role where your medical expertise will directly influence trial design, patient safety, and regulatory strategy-driving therapies that could transform lives.
Why This Role Stands Out Lead late-stage clinical trials with direct influence on strategy and execution Work across disciplines to bring innovative treatments to market Engage with key opinion leaders and regulatory authorities at the forefront of endocrinology What You'll Do
Contribute to and execute the Clinical Development Plan for obesity programs Serve as Medical Monitor, ensuring patient safety and data integrity in late-phase trials Lead trial design and provide guidance to study teams, sites, and investigators Collaborate on critical clinical documents including protocols, investigator brochures, and regulatory submissions Interpret and communicate clinical data to drive decision-making Partner with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs Maintain strong external relationships with KOLs, clinical consultants, and investigative sites What You Bring
MD (Board Certification or PhD in Endocrinology or related field preferred) 5+ years of industry experience (or equivalent academic/clinical background); candidates with less experience may be considered for an Associate Medical Director role 3+ years in clinical trial design and execution Proven ability to manage safety monitoring, data analysis, and cross-functional collaboration Excellent written and verbal communication skills Strong leadership and problem-solving capabilities Ability to work in a fast-paced, high-accountability environment
United States (Remote)
A growing biotech with an expanding late-phase pipeline is seeking an
experienced Medical Director
to lead clinical development efforts in endocrinology, with a focus on obesity. This is a high-impact role where your medical expertise will directly influence trial design, patient safety, and regulatory strategy-driving therapies that could transform lives.
Why This Role Stands Out Lead late-stage clinical trials with direct influence on strategy and execution Work across disciplines to bring innovative treatments to market Engage with key opinion leaders and regulatory authorities at the forefront of endocrinology What You'll Do
Contribute to and execute the Clinical Development Plan for obesity programs Serve as Medical Monitor, ensuring patient safety and data integrity in late-phase trials Lead trial design and provide guidance to study teams, sites, and investigators Collaborate on critical clinical documents including protocols, investigator brochures, and regulatory submissions Interpret and communicate clinical data to drive decision-making Partner with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs Maintain strong external relationships with KOLs, clinical consultants, and investigative sites What You Bring
MD (Board Certification or PhD in Endocrinology or related field preferred) 5+ years of industry experience (or equivalent academic/clinical background); candidates with less experience may be considered for an Associate Medical Director role 3+ years in clinical trial design and execution Proven ability to manage safety monitoring, data analysis, and cross-functional collaboration Excellent written and verbal communication skills Strong leadership and problem-solving capabilities Ability to work in a fast-paced, high-accountability environment