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Clinical Program Manager Jobs in Delaware (NOW HIRING)

Ob Hospitalist Group

OB/GYN Site Director

Lewes, DE

... program at a partner hospital. This leadership role combines direct clinical care with operational oversight, team development, and hospital relationship management. The Site Director will ensure ...

Powerback Rehab

Program Lead-PB Rehab PTA

Dover, DE · On-site

Powerback Rehabilitation Program Lead At Powerback, we're on a mission to improve lives. As the ... Ensures that the clinical management of the rehabilitation department, including oversight related ...

Geneis Healthcare

Program Lead-PB Rehab PTA

Dover, DE · On-site

Powerback Rehabilitation Program Lead At Powerback, we're on a mission to improve lives. As the ... Ensures that the clinical management of the rehabilitation department, including oversight related ...

ICON

Biospecimen Operations Manager

Wilmington, DE · On-site

... program meetings with central lab, clinical, operations and data management. * Contribute to ... activities involving the Data Management team, including eCRF set-up, database build for sites and ...

Icon plc

Biospecimen Operations Manager

Wilmington, DE · Hybrid

... program meetings with central lab, clinical, operations and data management. * Contribute to ... activities involving the Data Management team, including eCRF set-up, database build for sites and ...

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Showing results 21-40

All JobsClinical Program JobsClinical Program Manager JobsClinical Program Manager Jobs in Delaware

Clinical Program Manager information

See Delaware salary details

$44.5K

$92.7K

$149.6K

How much do clinical program manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for clinical program manager in Delaware is $92,683.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,600.00 and $105,100.00 per year, depending on experience, location, and employer.

What degree do I need to be a clinical program manager?

A clinical program manager typically needs at least a bachelor's degree in a healthcare-related field such as nursing, public health, or healthcare administration. Many employers prefer candidates with a master's degree in healthcare administration, business, or a related discipline, along with relevant experience and strong organizational skills.

How does a clinical program manager typically collaborate with cross-functional teams to ensure successful clinical trial execution?

A Clinical Program Manager works closely with cross-functional teams, including clinical research associates, data managers, regulatory affairs, and medical monitors, to coordinate all aspects of clinical trials. They facilitate regular meetings, ensure clear communication, and resolve any issues that may affect timelines or data quality. This role is pivotal in aligning diverse team members toward shared goals, managing expectations, and adapting to evolving study requirements, which helps drive successful trial outcomes.

What is the difference between Clinical Program Manager vs Clinical Project Manager?

AspectClinical Program ManagerClinical Project Manager
CredentialsTypically requires a clinical background, such as RN, MSN, or related healthcare degree, along with project management certificationOften requires a project management certification (PMP) or equivalent; clinical background is preferred but not always mandatory
Work EnvironmentOversees multiple related projects within a clinical program, often in healthcare organizations or pharmaceutical companiesManages individual clinical trials or projects, usually within a larger program or portfolio
Employer & Industry UsageCommonly employed in healthcare, biotech, and pharmaceutical industries to coordinate broad clinical initiativesUsed across similar industries to manage specific clinical studies or trials

The Clinical Program Manager focuses on overseeing multiple related clinical projects and strategic initiatives, while the Clinical Project Manager manages individual clinical trials. Both roles require project management skills, but the Program Manager has a broader scope and strategic responsibilities.

What does a clinical program manager do?

A clinical program manager oversees the planning, implementation, and management of clinical trials and research programs. They coordinate teams, ensure compliance with regulatory standards, and monitor project progress using tools like project management software. Strong organizational, communication, and regulatory knowledge are essential for success in this role.

What is a clinical program manager?

A Clinical Program Manager is a professional responsible for overseeing the planning, coordination, and execution of clinical trials or healthcare programs within a medical or research organization. They ensure that clinical projects meet regulatory, ethical, and organizational standards, while managing timelines, budgets, and cross-functional teams. Clinical Program Managers also liaise with stakeholders, analyze data, and report on project progress to ensure successful outcomes. Their role is critical in advancing medical research and improving patient care.

How much do clinical program managers make?

Clinical Program Managers typically earn an average salary of around $100,000 to $130,000 annually, depending on experience, education, and the size of the organization. Salaries can vary based on location, with higher compensation often found in regions with a higher cost of living, and may include benefits such as bonuses and health insurance.

What are the key skills and qualifications needed to thrive as a clinical program manager?

To thrive as a Clinical Program Manager, you need a solid background in clinical research or healthcare management, often supported by a relevant degree and experience in program coordination. Familiarity with clinical trial management systems (CTMS), regulatory compliance protocols, and sometimes certifications like PMP or CCRA are commonly required. Strong leadership, organizational skills, and effective communication set top performers apart in this role. These skills are crucial for overseeing complex clinical programs, ensuring regulatory adherence, and leading multidisciplinary teams toward successful project outcomes.
What are the most commonly searched types of Clinical Program jobs in Delaware? The most popular types of Clinical Program jobs in Delaware are:
What are popular job titles related to Clinical Program Manager jobs in Delaware? For Clinical Program Manager jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Clinical Program Manager jobs in Delaware look for? The top searched job categories for Clinical Program Manager jobs in Delaware are:
What cities in Delaware are hiring for Clinical Program Manager jobs? Cities in Delaware with the most Clinical Program Manager job openings:
Clinical Program Manager jobs near you
Infographic showing various Clinical Program Manager job openings in Delaware as of July 2026, with employment types broken down into 85% Full Time, and 15% Temporary. Highlights an 100% In-person job distribution, with an average salary of $92,683 per year, or $44.6 per hour.

Director, Clinical Operations

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 27 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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