Clinical Trials Project Manager

The Opportunity: Help turn clinical-trial education into clearer pathways to information, referrals, and support. The Clinical Trials Project Manager manages the day-to-day execution of approved initiatives within Tigerlily’s SPARK Center of Excellence, coordinating projects, participant follow-up, partner deliverables, educational resources, and clinical-trial components of organizational events. This hands-on role is well suited to an organized project manager who builds strong working relationships, follows through on details, and cares about equitable access. Working under CEO direction and established project management standards, you will translate approved priorities into practical work plans, resolve routine operational issues, and recommend improvements based on community feedback and program data.

Key Responsibilities: Manage assigned SPARK projects from planning through closeout, tracking milestones, owners, deadlines, dependencies, and deliverables in Monday.com and other approved tools. Coordinate program administration, including calendars, meetings, agendas, decision records, action items, files, contact lists, and approval trackers; route contracts, invoices, and purchase requests to authorized owners. Coordinate approved Clinical Trial Match, interest collection, matching, referral, and follow-up workflows with community members and authorized research, healthcare, and navigation partners. Track inquiries, next steps, unresolved items, and access barriers. Serve as the operational contact for assigned sponsor and research partner activities, coordinating meetings, tracking approved commitments, and supporting timely reporting. Coordinate the clinical-trial component of approved events with host teams and other departments, including materials, partner readiness, assigned contributors, approved data collection, and post-event follow-up. Coordinate development, qualified review, approval, distribution, and maintenance of educational resources, including Make It Make Sense, Clinical Trial Match, toolkits, newsletters, website content, and resource library materials. Maintain accurate project and program records in approved systems, including SharePoint. Prepare weekly updates and periodic summaries of progress, referrals, follow-up, resource reach, partner deliverables, risks, and decisions needed. Follow approved privacy, confidentiality, consent, security, and records practices; promptly escalate participant-safety, compliance, delivery, and data concerns to designated owners. Identify workload conflicts, unclear ownership, and resource needs; recommend practical improvements and maintain procedures, handoff materials, and continuity records. This role coordinates education and access pathways. It does not provide medical advice, determine clinical-trial eligibility, or conduct formal screening, informed consent, or enrollment. Those responsibilities remain with authorized clinical or research professionals. Strategy, staffing, funding, and material external commitments remain subject to leadership approval.

Qualifications: Bachelor’s degree in public health, health administration, life sciences, nonprofit management, or a related field, or an equivalent combination of relevant education and experience. At least three years of relevant program or project experience managing timelines, stakeholder coordination, documentation, and reporting. Working knowledge of clinical-trial education, referral pathways, or community health access, including clinical and compliance boundaries. Strong organizational, written and verbal communication, relationship coordination, and data accuracy skills, with sound participant-centered judgment. Ability to prioritize competing demands, identify risks, and coordinate initiatives involving multiple stakeholders within established authority. Proficiency with Microsoft 365 and collaborative project management tools, with the ability to learn Monday.com and SharePoint. Preferred experience includes oncology, breast cancer, women’s health, health equity, patient navigation, or advocacy; clinical-trial access or research partnerships; work with historically underserved communities; nonprofit sponsor or grant reporting; and developing procedures and using program data and feedback to improve workflows. How We Work Tigerlily’s leadership behaviors are Own, Lead, Deliver, and Grow. In this role, that means taking responsibility for assigned work, creating clarity for collaborators, delivering approved priorities, and using learning and feedback to strengthen access and program effectiveness. Compensation Proposed base salary: $75,000–$85,000 annually, subject to final market validation. Placement within the approved range will be based on relevant experience and overall qualifications.

Benefits: Tigerlily Foundation offers a competitive benefits package including medical, dental, vision, retirement, and paid time off benefits. Work Environment and Travel This is a remote position requiring regular collaboration with colleagues, community members, and external partners. Travel to support approved programs, meetings, and events is required. Occasional evening and weekend work is also required based on program and event schedules. Apply Interested candidates should apply through this LinkedIn job posting and submit a resume and cover letter highlighting a relevant program or project and their approach to improving clinical-trial education or access. Applications will be reviewed on a rolling basis. Tigerlily Foundation is an Equal Opportunity Employer committed to building a diverse and inclusive workplace. We do not discriminate on the basis of any protected characteristic under applicable federal, state, or local law. Reasonable accommodations are available for qualified individuals with disabilities.