Technical Delivery Manager (Remote)

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe.   

Position Summary

The Technical Delivery Manager is responsible for delivering technology products and enterprise implementations across START's clinical research operations. Reporting to the Sr. Director of Business Relationship and Delivery, this role manages the requirements, planning, and execution of assigned product initiatives from inception through go-live. The Product Manager engages directly with clinical, operations, and IT stakeholders to gather and document requirements, manage backlogs, coordinate delivery teams, and ensure that implementations are completed on time, within scope, and deliver intended value. This role is expected to operate with a high degree of initiative and ownership, with opportunity to grow into broader product responsibilities over time.

This is a remote role. The salary range for this role is $110,000 - $125,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 

Work Hours: M-F, 8am-5pm 

Location: Remote

Essential Responsibilities

• Manage the full delivery lifecycle for assigned products and implementations, from requirements gathering through launch and initial post-go-live support.
• Engage with stakeholders across clinical, operations, and IT teams to gather, document, and validate detailed business and functional requirements.
• Develop and maintain project plans, delivery timelines, and status reports for assigned initiatives and implementations.
• Coordinate with technology teams, vendors, and implementation partners to ensure alignment on scope, schedule, and deliverables.
• Track and communicate project progress, risks, and issues; escalate blockers and cross-team dependencies to the Sr. Director of Business Relationship and Delivery as appropriate.
• Ensure that user acceptance testing (UAT) is planned, coordinated, and completed prior to go-live; obtain stakeholder sign-off on deliverables.
• Support change management and adoption activities including training coordination, user communications, and documentation.
• Produce dashboards, metrics, and status updates for stakeholder review.
• Identify opportunities for process improvements and contribute to the development of product and delivery standards.

Required Education and Experience

• Bachelor's degree in Business Administration, Information Technology, or a related field.
• 3+ years of experience in product management, business analysis, IT project management, or technology delivery.
• Demonstrated experience gathering and documenting requirements and managing backlogs in a cross-functional environment.
• Familiarity with software development lifecycle (SDLC) processes.
• Experience with Agile, Waterfall, or hybrid project methodologies.
• Strong written and verbal communication skills with the ability to engage both technical and non-technical stakeholders.
• Proficiency in creating status reports, dashboards, and project documentation.
• Experience with project and product management tools such as Jira, Confluence, or equivalent platforms.

Preferred Education and Experience:

• Experience in clinical research, oncology, life sciences, or a regulated healthcare environment preferred.
• Certified Business Analysis Professional (CBAP), Certified Scrum Product Owner (CSPO), or equivalent certification preferred.
• Six Sigma Yellow Belt or other process improvement certification preferred.

Physical and Travel Requirements

• Approximately 80% of time is spent sitting.
• Very fast-paced and ever-changing healthcare environment.
• Demanding deadlines and time frames.
• Constant demand for updating knowledge.
  

Best-in-Class Benefits and Perks  

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:  

• 401(k) retirement savings plan with employer match  

• Eligibility for an annual performance bonus, based on role and company results  

• Generous paid time off and paid holidays  

• Comprehensive medical, dental, and vision coverage and optional insurance options  

• Company paid life and disability insurance for added financial protection  

• Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one  

• Flexible FSA and HSA plans to support your financial wellness  

• Commitment to a supportive environment that values balance, wellbeing, and flexibility  

• We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.  

More About START  

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites.

Learn more at STARTresearch.com.   

Ready to be part of a team changing the future of cancer treatment?  

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.  

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.