Clinical Program Operations Manager, Therapeutics & Innovations

Job Title: Clinical Program Operations Manager, Therapeutics & Innovations

Location: Remote 

Type: Full-Time

Travel: Up to ~25% (primarily to clinical sites, investigator meetings, and key partner locations)

 

 

About the Role

We are seeking a hands-on, execution-focused Clinical Program Operations Manager with deep experience in oncology and clinical trial operations to lead the day-to-day delivery and execution of our therapeutic clinical programs. This role is central to ensuring our studies move forward with precision, on schedule, within scope, and aligned with company goals. You will manage complex timelines, coordinate cross-functional efforts, and support external relationships critical to clinical delivery.

 

This is a high-impact opportunity for someone who thrives in a fast-moving environment. You’ll bring strong oncology trial experience, a solution-first mindset, and the ability to drive clarity and progress even when priorities shift.

 

If you need structure to act, wait for permission to lead, or hesitate in chaos, this isn’t the role for you. We’re looking for someone sharp, solution-obsessed, and relentless about execution, someone who moves fast, thrives in ambiguity, and gets things done without excuses.

 

Key Responsibilities

 

Program Execution & Timeline Management

• Own, drive, and enforce comprehensive trial timelines, deliverables, and Gantt charts; ensure alignment across functions and hold teams accountable for execution.

 

• Identify risks early and fix them fast.

 

• Collaborate closely with internal functions (e.g., clinical operations, regulatory, quality, medical) and external CROs/vendors.
  

• Ensure real-time visibility of program status for leadership and cross-functional partners by developing dashboards, trackers, and milestone reports, implementing structured tracking systems, and monitoring cross-functional timelines to manage dependencies and deliverables.

 

Operational Leadership

• Oversee study startup activities, including site selection, feasibility, and trial initiation.
  

• Manage CRO relationships and performance, including KPIs, deliverables, and contracts.
  

• Ensure operational readiness for investigator meetings, site visits, and data reviews, in collaboration with cross-functional teams.

 

• Dive into the weeds when necessary and eliminate roadblocks without being asked.

 

• Create and maintain standardized project management templates (e.g., dashboards, trackers, reporting tools) to streamline team workflows

 

Stakeholder Engagement & Field Leadership

• Serve as the primary operational liaison for internal and external trial communications.
  

• Prepare structured updates, dashboards, and risk logs for senior leadership and the steering committee.
  

• Travel (up to ~25%) to clinical sites, CROs, investigator meetings, and key partners to ensure operational excellence, build relationships, and represent clinical leadership on the ground.

 

• Foster strong relationships with investigators and site personnel to ensure engagement and performance.
  
  

Scientific Contribution

• Attend data review meetings and contribute to clinical insight generation and action plans.
  

• Help translate scientific and clinical objectives into executable operational strategies and trial designs.

 

 

Qualifications

• Advanced degree (PhD, PharmD, MD, or MS) in a life science or clinical field is required.
  

• Minimum 5 years of experience in clinical research with