SR AD / Director, Clinical Development Operations Lead (CDOL/SR CDOL), Obesity at Jobgether – United States
Explore Related Opportunities
About This Position
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a SR AD / Director, Clinical Development Operations Lead (CDOL/SR CDOL), Obesity in the United States.
This role provides an opportunity to lead operational strategy and execution for late-phase clinical programs within the obesity and MASH therapeutic areas. You will work at the intersection of Clinical Operations, Statistics, Regulatory Affairs, and Drug Safety to design efficient, data-driven trial strategies that ensure timely, high-quality execution. The position emphasizes patient-centric approaches, innovative trial design, and adoption of digital technologies, providing measurable impact across global programs. You will collaborate with cross-functional stakeholders, manage feasibility and risk assessments, and ensure effective engagement with clinical trial sites. Operating in a dynamic, matrixed environment, this role is suited for strategic thinkers who can drive complex clinical trials while fostering team alignment and operational excellence. Both Senior Associate Director and Director-level candidates will have the opportunity to shape program delivery and advance clinical development outcomes at scale.
Lead clinical program execution and provide operational input into late-phase Clinical Development Plans (CDPs) for obesity and MASH programs.
Develop and implement operational strategies, including timelines, country/site selection, and vendor sourcing models.
Partner with cross-functional stakeholders to ensure efficient, consistent, and non-redundant trial execution.
Drive adoption of innovative trial designs, digital tools, and data-driven decision-making.
Ensure patient-centric approaches and maintain expert engagement with clinical trial sites.
Identify feasibility risks, mitigation strategies, and external vendor requirements prior to trial initiation.
Provide leadership and guidance to trial teams, communicate strategic objectives, and monitor trial performance.
Requirements:
Senior Associate Director (CDOL): Bachelor’s degree required; Master’s preferred, with 10+ years in clinical development or clinical operations.
Director (SR CDOL): PhD or MD with 5+ years therapeutic area experience, or Bachelor’s/Master’s with 15+ years clinical trial experience.
Extensive experience in obesity and/or MASH clinical programs strongly preferred.
Proven leadership of complex, global clinical trial programs across all stages of drug development.
Deep understanding of global regulatory, ethical, and compliance requirements.
Strong strategic thinking, communication, and stakeholder management skills.
Ability to lead effectively in matrixed, cross-functional teams with a patient-focused mindset.
Legally authorized to work in the United States and willing to comply with post-offer requirements.
Benefits:
Competitive base salary range: $170,000 – $269,000 for CDOL; $200,000 – $316,000 for SR CDOL.
Eligibility for role-specific discretionary bonus, relocation, and additional compensation elements.
Comprehensive health, dental, and vision insurance plans.
Retirement benefits including 401(k) or equivalent with company contributions.
Paid time off, parental leave, and flexible work arrangements.
Opportunities for professional development, networking, and career growth within global clinical development.
Supportive, collaborative environment emphasizing work-life balance and meaningful contributions to patient care.