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.
Apply NowOpens the employer's application page

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.
View Full Description & ApplyYou'll be redirected to the employer's site
$143,300–$193,300, depending on qualifications, experience, skills, education, certifications, and work location.
Apply Now