Jacobs Management Group, Inc.
Senior Medical Director - Clinical Research
Step into a pivotal leadership role where clinical excellence meets innovation. As Senior Medical Director with my client, you’ll be at the heart of groundbreaking research, guiding trials that shape the future of medicine. This is your chance to impact lives by advancing therapies in adult chronic disease and beyond.
Why You Should Apply
Lead high-impact clinical trials across multiple therapeutic areas
Collaborate with top-tier sponsors and CROs in a dynamic research environment
Influence strategic growth and community partnerships
Mentor junior investigators and shape the future of clinical research
Comprehensive benefits including health, dental, vision, and 401(k)
Relocation assistance available for the right candidate
What You’ll Be Doing
Serve as Principal Investigator and medical authority for clinical trials
Oversee protocol execution and ensure regulatory compliance
Build strategic partnerships with community organizations and physicians
Guide feasibility assessments and site selection for new studies
Provide medical oversight, training, and risk assessments for ongoing trials
About You
Be able to do the job as described
Board-certified MD or DO with active U.S. medical license
Experience managing GLP-1 studies of 12+ months
Skilled in adult chronic disease management within a community setting
Proficient in clinical trial master filing systems and eSource platforms
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Why You Should Apply
Lead high-impact clinical trials across multiple therapeutic areas
Collaborate with top-tier sponsors and CROs in a dynamic research environment
Influence strategic growth and community partnerships
Mentor junior investigators and shape the future of clinical research
Comprehensive benefits including health, dental, vision, and 401(k)
Relocation assistance available for the right candidate
What You’ll Be Doing
Serve as Principal Investigator and medical authority for clinical trials
Oversee protocol execution and ensure regulatory compliance
Build strategic partnerships with community organizations and physicians
Guide feasibility assessments and site selection for new studies
Provide medical oversight, training, and risk assessments for ongoing trials
About You
Be able to do the job as described
Board-certified MD or DO with active U.S. medical license
Experience managing GLP-1 studies of 12+ months
Skilled in adult chronic disease management within a community setting
Proficient in clinical trial master filing systems and eSource platforms
#J-18808-Ljbffr