Associate Director, Collaborative Operations for Health Engagement
New
J
JobgetherClinical Research
Based in the United States... located on the U.S. West Coast and working in the Pacific Time Zone, Pacific Time ZoneFull-TimeManager
Salary$143,300–$193,300, depending on qualifications, experience, skills, education, certifications, and work location.
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Job Details
- Experience
- At least 8 years of relevant clinical research operations experience.
- Required Skills
- Project ManagementData AnalysisStakeholder management
Requirements
- Bachelor’s degree required (graduate degree such as MBA, MSc, PhD, MD, or MPH preferred).
- At least 8 years of relevant clinical research operations experience.
- Understanding of clinical trial study planning, feasibility, site strategy, and enrollment.
- Demonstrated ability to translate strategic priorities into practical, scalable operations.
- Strong analytical and data interpretation skills (epidemiology, real-world data).
- Experience developing or using dashboards, scorecards, and performance indicators.
- Cross-functional collaboration skills and ability to influence stakeholders.
- Experience identifying clinical trial participation barriers and improving patient engagement.
- Strong project and workstream management capabilities.
- Excellent communication and presentation skills.
- Ability to work effectively in evolving or ambiguous environments.
- Candidates must be located on the West Coast of the United States within the Pacific Time Zone.
Responsibilities
- Support the development and evolution of the COHERE strategy, operating model, and processes.
- Translate strategic objectives into scalable operational approaches for clinical research programs.
- Integrate patient access considerations into early study planning, feasibility, and enrollment strategies.
- Analyze real-world data and patient journey insights to identify participation barriers.
- Develop dashboards and performance metrics to support site selection and study execution.
- Partner with internal clinical, regulatory, and medical teams to monitor enrollment and identify risks.
- Build strategic relationships with research sites, advocacy groups, and community organizations.
- Represent the organization at industry forums, scientific congresses, and site meetings.
- Manage assigned workstreams, consultants, and external vendors.
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