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Director Of Clinical Project Management

10+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Director of Clinical Project Management

Location: San Francisco Bay Area (Campbell, CA)
Company: Lumicity
Job Type: Full-time, On-site
Posted: 2 weeks ago
Applicants: 34


Job Description:

Position Overview:
As the Director of Clinical Project Management, you will lead the planning, execution, and delivery of complex, multi-phase clinical research initiatives. You will oversee end-to-end project management of global clinical studies, supporting high-performance teams while collaborating cross-functionally with operations, product, regulatory, and commercial teams.


Key Responsibilities:

  • Lead and manage the execution of clinical studies involving a proprietary digital health platform.

  • Develop integrated project plans aligned with business goals, regulatory frameworks, and client expectations.

  • Act as the primary point of contact for internal stakeholders and external partners, including sponsors, CROs, vendors, and clinical sites.

  • Supervise and mentor Clinical Project Managers and support staff, fostering a culture of collaboration and continuous improvement.

  • Coordinate closely with quality, product, and engineering teams to translate clinical needs into actionable plans.

  • Monitor key project metrics, including timelines, budgets, resources, and deliverables.

  • Contribute to the development of study tools, training materials, and documentation for internal and external use.

  • Represent the company in client meetings, audits, industry events, and regulatory interactions as necessary.

  • Identify risks proactively and implement contingency plans to ensure smooth project execution.

  • Manage the deployment of new technology to clinical sites.


Requirements:

  • 10+ years of progressive experience in clinical project management in medical device, pharmaceutical, or digital health settings.

  • Hands-on experience working across sponsor, site, and vendor/CRO environments.

  • Proven track record in managing global or multi-site clinical studies, from preclinical through post-market phases.

  • Familiarity with decentralized or hybrid clinical trials, including remote data collection and digital endpoints.

  • Strong understanding of clinical operations, protocol development, regulatory submissions, and study execution.

  • Effective communicator with experience managing complex, cross-functional projects and executive-level stakeholders.

  • Proficiency in clinical project management tools (e.g., Smartsheet, Asana, Jira, Workday) and MS Office/Google Workspace.

  • Bachelor's degree required; advanced degree or PMP certification preferred.

Preferred Experience:

  • Experience with connected devices, digital biomarkers, or eClinical platforms.

  • Background in med-tech, wearables, and/or SaMD (Software as a Medical Device).

  • Familiarity with FDA, EMA, and global regulatory processes.


What We Offer:

  • Competitive base salary with bonuses and equity.

  • Medical, dental, and vision insurance.

  • 401(k) with company matching.

  • Generous PTO policy.

  • Professional development support.

  • Opportunity to work on innovative healthcare solutions with real-world impact.