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Director Clinical Project Management Jobs in Delaware

Truveris

Clinical Director

Wilmington, DE · On-site +1

$160K - $175K/yr

As a Clinical Director, you support the Account Team through the RFP process, conduct clinical ... Strong project management and quality assurance skills * Experience managing multiple deliverables ...

HK Recruiting

Program Director R&D PMO

Newark, DE · On-site +1

As Program Director, R&D PMO, you will provide strategic program management and operational leadership for the execution of high-impact programs, guiding them from development through ...

Hologic Inc.

Program Director, R&D PMO

Newark, DE · On-site +1

$170K - $303K/yr

As Program Director, R&D PMO , you will provide strategic program management and operational leadership for the execution of high-impact programs, guiding them from development through ...

ATI Restoration

Project Director

Wilmington, DE · On-site

Project Director FLSA Status: Salaried, Exempt Status: Full-Time Position Summary The Project ... Support Project Manager to resolve scope discrepancies and customer concerns; ensure project ...

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Director Clinical Project Management information

See Delaware salary details

$18K

$124.5K

$183.2K

How much do director clinical project management jobs pay per year?

As of Aug 9, 2026, the average yearly pay for director clinical project management in Delaware is $124,486.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,100.00 and $147,600.00 per year, depending on experience, location, and employer.

What does a director of clinical project management do?

A Director of Clinical Project Management oversees the planning, execution, and completion of clinical trials within a pharmaceutical or biotech company. They lead project management teams, ensure regulatory compliance, manage budgets and timelines, and coordinate communication among stakeholders. Their responsibilities also include risk management, resource allocation, and ensuring trials meet both scientific and business objectives. This role is critical for bringing new medical treatments through the development pipeline to market approval.

What are the key skills and qualifications needed to thrive as a director of clinical project management, and why are they important?

To thrive as a Director of Clinical Project Management, you need deep expertise in clinical research, regulatory compliance, project leadership, and typically an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or CCRP are commonly required. Strong strategic thinking, communication, and team leadership skills help drive project success and foster collaboration among cross-functional teams. These competencies are vital for delivering clinical trials on time, within budget, and in compliance with regulatory standards.

What is the difference between Director Clinical Project Management vs Clinical Project Manager?

AspectDirector Clinical Project ManagementClinical Project Manager
ResponsibilitiesOversees multiple projects, strategic planning, team leadershipManages individual clinical trials, day-to-day operations
Experience & CredentialsTypically requires 8+ years, advanced degrees, leadership experienceUsually 3-5 years, relevant clinical or project management certifications
Work EnvironmentSenior management, cross-functional teams, strategic meetingsProject teams, site coordination, operational tasks

The main difference is that the Director Clinical Project Management holds a senior leadership role overseeing multiple projects and strategic initiatives, while the Clinical Project Manager focuses on managing individual clinical trials and operational activities. Both roles require relevant experience and certifications, but the director's scope is broader and more strategic.

What are some common challenges faced by a director of clinical project management, and how can they be addressed?

Directors of Clinical Project Management often encounter challenges such as managing complex, multi-site trials, maintaining regulatory compliance, and coordinating cross-functional teams. Balancing timelines, budgets, and quality expectations can also be demanding, especially when unexpected issues arise. Successful directors address these challenges by fostering clear communication, utilizing robust project management tools, and building strong relationships with stakeholders. Staying current with regulatory changes and providing mentorship to team members also helps ensure project success and professional growth.
What are popular job titles related to Director Clinical Project Management jobs in Delaware? For Director Clinical Project Management jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Director Clinical Project Management jobs in Delaware look for? The top searched job categories for Director Clinical Project Management jobs in Delaware are:
What cities in Delaware are hiring for Director Clinical Project Management jobs? Cities in Delaware with the most Director Clinical Project Management job openings:
Director Clinical Project Management jobs near you

Director, Clinical Operations

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 28 days ago

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Job Summary (Primary function)
The Director, Clinical Operations provides strategic, operational, and people leadership for global Phase I-III clinical trials, including first-in-human and pivotal studies. This role oversees end-to-end clinical trial execution, ensures compliance with FDA/EMEA regulations and ICH-GCP, manages CROs and vendors, and partners cross-functionally to deliver high-quality clinical programs aligned with corporate objectives. The Director also leads Clinical Operations staff, drives operational excellence, and contributes to program-level planning across Incyte's Hematology, Oncology, and Inflammation/Autoimmunity portfolio.
Essential Functions of the Job (Key responsibilities)
  • Provide strategic operational leadership for assigned clinical programs, including feasibility, resource forecasting, and long-range planning.
  • Contribute to program-level strategy, timelines, budgets, and operational deliverables in alignment with corporate goals.
  • Ensure harmonized operational plans and high-quality data across global trials.
  • Lead end-to-end planning, implementation, and management of global Phase I-III trials, including first-in-human studies.
  • Oversee day-to-day clinical operations to ensure adherence to timelines, budgets, SOPs, ICH-GCP, and country-specific regulations.
  • Manage investigational product accountability and reconciliation processes.
  • Support preparation of safety updates, interim analyses, and final clinical study reports; resolve data discrepancies.
  • Partner closely with Clinical Development, Regulatory, Biometrics, Supply Chain, and other internal teams to achieve study objectives.
  • Lead and/or participate in cross-functional study team meetings, ensuring alignment and timely decision-making.
  • Collaborate with senior management to determine clinical supply requirements and operational strategy.
  • Select, negotiate, and manage CROs and external vendors (central labs, EDC providers, patient recruitment partners, etc.).
  • Develop RFPs, conduct cost analyses, and ensure vendor performance meets quality, timeline, and budget expectations.
  • Provide strategic oversight of CRO governance and issue resolution.
  • Contribute to the development and review of protocols, amendments, ICFs, CRFs, study guides, operational plans, and charters.
  • Participate in preparation of INDs, Investigator Brochures, regulatory briefing documents, and other clinical submissions.
  • Ensure operational feasibility and high-quality clinical data across studies.
  • Build and maintain strong relationships with investigator sites, KOLs, patient advocacy groups, and referral networks.
  • Support site engagement strategies to ensure enrollment targets and study goals are met.
  • Recruit, manage, and mentor Clinical Trial Managers, Clinical Trial Specialists, and other direct reports.
  • Provide clear objectives, ongoing coaching, and performance evaluations.
  • Foster a culture of engagement, accountability, and collaboration.
  • Provide regular updates and status reports to senior leadership.

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Bachelor's degree in Life Sciences or related field required.
  • 10+ years of clinical operations experience in biopharma or biotech.
  • Minimum 5 years of direct clinical study management experience.
  • Extensive experience managing global Phase I-III trials; first-in-human experience strongly preferred.
  • Oncology experience preferred; rare disease experience desirable.
  • Global clinical development experience preferred.
  • Strong knowledge of FDA/EMEA regulations, ICH-GCP, and clinical trial methodology.
  • Proven ability to manage CROs and external vendors.
  • Experience with clinical systems (EDC, CTMS, eTMF) and operational documentation.
  • Demonstrated ability to manage budgets, timelines, and complex operational plans.
  • Proven ability to lead and develop high-performing teams.
  • Strong organizational, time-management, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Thrives in a collaborative, fast-paced, high-energy environment.
  • Ability to travel domestically and internationally (up to 30%).

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
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