Project Manager Jobs in Durham, NC

Manage multiple manufacturing projects across product development, upgrades, quality, cost reduction, and efficiency initiatives. Plan, execute, monitor budgets/schedules, track KPIs, mitigate risks, maintain documentation, and report status to stakeholders while coordinating resources and fostering team collaboration.

Lead utility-scale battery energy storage projects from contract execution through commercial operation. Coordinate engineering, software integration, supply chain, construction, commissioning, commercial, and customer teams while managing scope, schedule, budget, risk, quality, safety, and customer commitments. Implement PMO governance, project controls, stage-gate reviews, executive reporting, issue resolution, and continuous improvement across the project portfolio.

Lead and oversee medium-to-large multi-regional CNS clinical studies: develop study strategy and management plans, run bid defenses, manage budgets and risks, ensure ICH GCP and regulatory compliance, build client relationships, lead cross-functional teams, and mentor staff to drive milestones and quality deliverables.

Lead eCOA implementation projects through startup, managing timelines, budgets, stakeholder communications, vendor coordination, compliance with SOPs, risk mitigation, financial reporting, and process improvements while supporting onboarding and occasional travel for sponsor meetings.

Leads clinical study delivery from planning through execution, ensuring contractual, quality, timeline, and financial objectives are met. Builds and directs cross-functional project teams, manages risks, issues, vendors, scope changes, customer relationships, and study milestones. Develops study management plans, monitors performance, supports bid defenses, oversees project finances, implements corrective actions, and mentors less experienced team members. Applies clinical trial, drug development, regulatory, and therapeutic expertise to improve operational execution and customer satisfaction.

Leads startup implementation projects for electronic Clinical Outcome Assessments in clinical trials. Manages timelines, budgets, scope, invoices, risks, vendors, translations, configurations, compliance, and sponsor communications. Coordinates global cross-functional teams, presents project updates, drives process improvements, supports proposals, and mentors new hires. Requires occasional domestic or international travel for sponsor meetings.

Lead and deliver medium-to-large multi-regional oncology clinical studies: plan and execute study strategy, manage cross-functional teams, budgets, risks, quality, client relationships, and mentor staff to meet contractual and regulatory requirements.

The Project Manager will coordinate and manage clinical trials, overseeing technical, financial, and operational aspects to ensure quality delivery and project completion.

Lead multi-regional oncology clinical trials from planning through execution. Develop study strategy and integrated management plans, manage budgets and risks, oversee cross-functional teams, ensure ICH GCP and regulatory compliance, maintain client relationships, mentor staff, and drive project delivery, quality, and cost optimization.

Lead Phase I clinical trial projects, managing scope, schedule, budget, risk, quality and stakeholder communications. Oversee cross-functional teams, mentor junior PMs, support business development, and ensure regulatory and SOP compliance across global programs.

Leads Phase I clinical research projects from strategy through completion, managing scope, timelines, budgets, resources, risks, quality, client relationships, regulatory compliance, and contracted deliverables. Builds and mentors high-performing matrixed teams, oversees project governance and financial tracking, drives proactive issue resolution, and supports client presentations and change-order processes. Requires global clinical project management experience in a pharmaceutical or CRO environment.

As a Data Consultant, you will manage data quality solutions for benefit programs, lead project delivery, and coordinate with clients and internal teams to ensure successful outcomes.

As a Clinical Project Manager, you will facilitate the execution of clinical trials in Immuno-oncology and Cell & Gene Therapy, ensuring compliance with regulations and managing project teams and finances to improve patient outcomes.

The Senior Principal Project Manager leads new product development initiatives, ensuring project objectives are met while adhering to schedules and budgets. This role involves managing cross-functional teams, external partners, and applying technical knowledge for successful project execution.

Lead client-facing CDMO programs by coordinating internal teams, managing schedules and budgets, mitigating risks, driving scope changes, and maintaining client records to ensure on-time, compliant delivery and high client satisfaction.

Lead strategic delivery of complex global, multi-regional clinical trials from start-up through close-out. Guide cross-functional teams, manage timelines, budgets, quality, risks and regulatory compliance (ICH-GCP), and serve as primary sponsor partner to ensure study objectives and stakeholder alignment are met.

Lead planning and execution of medium-to-large multi-regional immuno-oncology clinical trials. Develop study strategy, manage budgets, risks, and timelines, ensure ICH GCP and regulatory compliance, build and lead cross-functional teams, serve as primary client contact, support bids, and mentor team members.

Lead end-to-end delivery of global real-world observational oncology studies within an FSP model: manage cross-functional teams, vendors, budgets, timelines, study documentation, regulatory compliance, risk mitigation, metrics reporting, and continuous improvement.

Manage low-to-medium complexity IT infrastructure projects end-to-end: deliverables, quality, schedule, budget, scope, governance, communications, risk, and client relationships. Ensure projects meet cost, time, and quality constraints while working on-site with clients.

Oversee technical project execution for microgrid solutions, managing communication, schedules, budgets, scope, engineering deliverables, design reviews, documentation, and production release signoffs. Coordinate daily with production engineering and cross-functional stakeholders including manufacturing, construction, procurement, and applications engineering. Establish project milestones, facilitate meetings, resolve technical roadblocks, and ensure deliverables meet project requirements before manufacturing release.

Manage survey project scope, schedule, budget, and quality. Coordinate stakeholders and municipalities, make technical survey/staking decisions, review deliverables, maintain client relationships, ensure crew safety, and mentor staff.

Manage end-to-end implementation of moderately complex eCOA clinical research projects, including scope, budgets, schedules, resources, quality, risks, documentation, vendors, and deliverables. Lead distributed internal teams, coordinate stakeholders and customers, provide technical direction for systems integration, communicate project status, and maintain client relationships. Ensure compliance with applicable standards and GCP principles, implement corrective actions, support product enhancement requests, and drive lessons learned and process improvements. International travel is required as needed.

Lead and deliver complex HR transformation initiatives for Networking HR, providing program leadership, governance, change management, stakeholder engagement, and executive-level decision support. Drive adoption of AI and emerging technologies, identify risks and dependencies, enable leader readiness, and ensure measurable business outcomes across integrated HR workstreams.

Manage New Technology Introduction (NTI) projects for SiC power products from concept through commercialization. Lead cross-functional teams to qualify devices to industrial and automotive standards, drive performance modeling, risk mitigation, testing, reliability, DFMEA/DVP&R, and handoff to operations. Coordinate schedules, material and fab starts, and communicate status and risks to stakeholders to ensure timely product release.

Lead and oversee operational aspects of Linguistic Validation and eCOA projects: create and track timelines, manage budgets and invoicing, report status and financials, coordinate cross-functional teams, ensure SOP compliance, mentor junior PMs, support proposals, and drive process improvements to meet quality and timeline metrics.