Lead challenging full-service global clinical research projects from startup to closure, ensuring delivery on time, within budget and to high quality standards. Manage and mentor multi-functional project teams, act as primary client contact, and support proposal/bid activities.
Lead multifunctional study management teams to deliver clinical trials on-time and on-budget while ensuring compliance with SOPs and GCP/ICH guidelines. Serve as primary client contact, monitor study metrics and finances, manage risks and resources, and support audits and team training.
Lead full-service phase II and III clinical research projects, managing deliverables, timelines and budgets while overseeing project teams. Support feasibility work and business development activities and implement company standard practices.
The Study Project Manager I leads cross-functional clinical study teams to plan and execute clinical research studies across development stages. They manage budgets, timelines, vendors and ensure compliance with quality standards while driving operational efficiencies and team development.
Lead and coordinate Global Medical Writing programs from early-stage through post-approval, integrating workstreams and maintaining project schedules and OKRs. Drive team collaboration, manage risks and budgets, and support governance and stakeholder reporting.
Serve as the main client contact for strategic accounts, bridging laboratory science and operations to deliver clinical trial projects. Support project planning, timelines, budgets, invoicing, reporting, and business development input while ensuring compliance with quality systems.
Lead and manage full-service Phase II and III clinical research projects including startup through closure. Supervise and mentor study staff, support feasibility and business development, and ensure project deliverables meet quality, timeline, and budget expectations.
Manage full-service clinical research projects in phases II and III, coordinating all project services from startup to closure. Lead and mentor project teams, support feasibility and business development, and ensure deliverables meet predefined quality standards.
Manage study startup, site onboarding, training, and operational oversight to ensure clinical studies run on time and meet quality and regulatory standards. Act as primary site contact, coach teams on GCP/ICH compliance, and escalate operational issues while supporting improvements to devices and workflows.
$90k - $110k
Zendesk
Asana
Sr. Project Manager - Clinical/Commercial Packaging, GMP, Drug Product
Senior Project Manager responsible for overseeing clinical and commercial packaging projects for drug product manufacturing under GMP conditions. The role manages project planning and execution, coordinates cross-functional teams, and ensures compliance with regulatory and quality requirements.
Manage medium-sized to large global clinical research projects from startup to closure, ensuring deliverables meet quality, timeline, and budget requirements. Lead and mentor project teams, act as primary escalation contact, participate in feasibility and business development activities.
Lead program-level laboratory and biospecimen activities, manage complex vendor relationships, and ensure regulatory and inspection readiness. Mentor staff, drive process improvements, and provide strategic input on vendor selection, contracts, and financials.
As a Clinical Lead Project Manager, you will manage global, multi-center clinical research projects, ensuring delivery on time and within budget while leading multi-functional project teams.
This role involves leading global Clinical Study Managers and ensuring alignment with organizational goals while managing clinical trials. The position requires collaboration across functions to drive program success and maintain high standards of delivery.
You will oversee study startup planning, site onboarding, and ongoing operational oversight to ensure studies are executed on time and to the highest standards. This role requires collaboration with sponsors, project teams, and clinical sites to drive efficient study execution.
As the Associate Director, Clinical Operations, you will be responsible for the strategic direction and operational planning of clinical trials. You will work with cross-functional teams to ensure efficient execution and compliance with regulatory guidelines.
As a Clinical Programmer/Analyst, you will design, build and review programming solutions that turn clinical and real-world data into clear, trustworthy results.
The Project Manager at Syneos Health supports overall project management of clinical studies, ensuring project scope, schedule, and cost are controlled.
$81k - $145k
Vice President - Strategic Accounts, Los Angeles/Hawaii
The Vice President - Strategic Accounts plays a critical role in advancing Caris Life Sciences’ enterprise precision medicine strategy by building, expanding, and sustaining system-level partnerships across surgery, pathology, and oncology.
$200k - $250k
Associate Clinical Quality Operations Manager, Oncology III