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Director Clinical Operations Jobs in Delaware (NOW HIRING)

Optigy

OB Hospitalist - Director Opportunity - Milford

Milford, DE · On-site

$120.50 - $159/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As part of the Ob Hospitalist clinical team, an Ob Hospitalist embraces delivering a quality OB Hospitalist program Value-Based culture. OB Site Director Role: Program Operations to ensure quality ...

Seaford Center

Assistant Director of Nursing, RN

Seaford, DE · On-site

$120K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Serve as a clinical operational liaison between the nursing units and the Director of Nursing. *Responsible for the quality of the clinical operations of the nursing units to include compliance with ...

Complete Care, Inc.

RN Assistant Director of Nursing

Dover, DE · On-site

$110 - $130/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Participate in care planning & ensure direct care providers follow established care plans, supplement hands on care needs Clinical Operations & Quality Assurance: Provides clinical documentation and ...

Complete Care at Silver Lake

RN Assistant Director of Nursing

Dover, DE · On-site

$60K - $80K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Participate in care planning & ensure direct care providers follow established care plans, supplement hands on care needs Clinical Operations & Quality Assurance: Provides clinical documentation and ...

HealthSouth

Director Therapy Operations

Middletown, DE · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Director of Therapy Operations Career Opportunity Highly regarded and esteemed for your Director of ... Develop and support clinical affiliations and relationships with educational institutions. * Use ...

State of Delaware

Nursing Director

Georgetown, DE · On-site

$89K - $148K/yr

Summary Statement The responsibilities of the Nursing Director include lead clinical support functions and clinical operations; optimizing care workflows and other service delivery; ensuring high ...

Elevance Health

Director Pharmacy Operations

Wilmington, DE · On-site

$125K - $165K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Director Pharmacy Operations Director Pharmacy Operations Location: This role requires associates ... Directs regional clinical program implementations and tracks call stats and interventions.

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Showing results 21-40

All JobsClinical Operations JobsDirector Clinical Operations JobsDirector Clinical Operations Jobs in Delaware

Director Clinical Operations information

See Delaware salary details

$60.1K

$146.1K

$282.7K

How much do director clinical operations jobs pay per year?

As of Aug 16, 2026, the average yearly pay for director clinical operations in Delaware is $146,095.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,100.00 and $173,600.00 per year, depending on experience, location, and employer.

What does a director of clinical operations do?

A director of clinical operations manages the daily operations of a healthcare facility or a specific department within a clinic or hospital. As a director of clinical operations, your responsibilities include scheduling staff to ensure proper coverage of patients and overseeing the productivity of your team to meet the organization's expectations. You define policies and procedures, facilitating further training when necessary. The director of clinical operations must also assess the performance of the medical team under your supervision regularly and mainstream processes when possible. Medical device manufacturers and pharmaceutical companies often hire a director of clinical operations to oversee research, lab, and testing operations.

What are the key skills and qualifications needed to thrive as a director of clinical operations?

To thrive as a Director of Clinical Operations, you need a robust background in clinical management, regulatory compliance, and healthcare administration, often supported by a relevant degree and substantial leadership experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like PMP or CCRA are commonly required. Exceptional leadership, strategic thinking, and communication skills help drive teams, manage stakeholders, and oversee complex projects. These skills are critical for ensuring clinical programs run efficiently, meet regulatory standards, and deliver high-quality patient outcomes.

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

AspectDirector Clinical OperationsClinical Project Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and extensive industry experienceUsually holds a bachelor's or master's degree in a related field, with relevant project management certifications
Work EnvironmentOversees multiple projects and teams across departments, strategic planningManages individual clinical trials, coordinates project activities, and timelines
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare companies for senior leadership rolesCommonly employed in clinical research organizations and pharmaceutical companies for trial management

The main difference is that the Director Clinical Operations focuses on strategic oversight and leadership across multiple clinical trials, while the Clinical Project Manager handles the day-to-day management of specific clinical studies. Both roles require strong industry knowledge, but the director position involves broader responsibilities and higher-level decision-making.

What does a director of clinical operations do?

A Director of Clinical Operations is responsible for overseeing the day-to-day management and strategic direction of clinical trials and research activities within healthcare organizations or pharmaceutical companies. They ensure that clinical studies are conducted efficiently, ethically, and in compliance with regulatory requirements. This role involves supervising teams, managing budgets, developing protocols, and liaising with stakeholders to ensure successful trial outcomes. Directors of Clinical Operations play a crucial role in bringing new medical treatments to market by ensuring studies run smoothly from start to finish.

How does a director of clinical operations typically collaborate with cross-functional teams to ensure successful clinical trial execution?

A Director of Clinical Operations regularly collaborates with cross-functional teams such as regulatory affairs, data management, medical affairs, and biostatistics to ensure clinical trials are executed on time, within budget, and in compliance with regulations. This role involves leading team meetings, aligning project timelines, and facilitating communication between internal stakeholders and external partners like CROs and vendors. Strong coordination skills are essential, as the Director must balance diverse priorities and resolve any operational issues that arise, ensuring all teams work toward shared objectives.
More about Director Clinical Operations jobs

What are the most commonly searched types of Clinical Operations jobs in Delaware?

The most popular types of Clinical Operations jobs in Delaware are:

What are popular job titles related to Director Clinical Operations jobs in Delaware?

For Director Clinical Operations jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Director Clinical Operations jobs in Delaware look for?

The top searched job categories for Director Clinical Operations jobs in Delaware are:

What cities in Delaware are hiring for Director Clinical Operations jobs?

Cities in Delaware with the most Director Clinical Operations job openings:

Director Clinical Operations jobs near you
Infographic showing various Director Clinical Operations job openings in Delaware as of August 2026, with employment types broken down into 82% Full Time, 14% Part Time, 1% Temporary, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $146,095 per year, or $70.2 per hour.

Field Clinical Advisor - Cell Therapy - Chicago (IL/WI/IN/MN)

AstraZeneca

Wilmington, DE • On-site

$203K - $305K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. FCAs focus on clinical study protocol expertise and education, optimizing the patient journey, and cell therapy pipeline engagement. We are looking for close collaboration with other CTCO Functions, Clinical Development, and Medical Affairs across multiple indications and departments to promote AstraZeneca's diverse cell therapy portfolio.
Summary
Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. FCAs focus on clinical study protocol expertise and education, optimizing the patient journey, and cell therapy pipeline engagement. We are looking for close collaboration with other CTCO Functions, Clinical Development, and Medical Affairs across multiple indications and departments to promote AstraZeneca's diverse cell therapy portfolio
You Will:
  • Pipeline mastery at scale: Build knowledge of AstraZeneca's cell therapy pipeline across multiple indications and assets. Convey AstraZeneca's cell therapy strategy, portfolio scope, and product differentiation; ensure compliant messaging across regions.
  • Systematically assess educational needs across owned sites, deliver advanced protocol training, and escalate patterns to Global Clinical Development with recommendations for enterprise solutions.
  • Capture applicable field insights (feasibility, operational bottlenecks, patient pathways) and deliver them to global and local partners to lead early risk identification and inform protocol/process adjustments.
  • Implement targeted protocol education (e.g., inclusion/exclusion criteria application) to lift enrollment rates, reduce screen failures, and minimize attrition.
  • Be the primary field point for protocol and clinical issues-evaluate and escalate, lead root-cause analysis, and implement corrective/preventive actions to reduce deviations and data queries.
  • Insight loop and continuous improvement: Systematically capture site-level insights, summarize trends for study teams and partners, and influence protocol/process adjustments and scaling.
  • Coordinate delivery across CTCO departments, Clinical Development, Medical Affairs, Supply/Logistics, Patient Operations, and Country Ops to ensure rapid, reliable service to partners and study sites.
  • Maintain current knowledge of local regulations, guidelines, codes of practice, and AstraZeneca policies; translate requirements into practical site actions and support inspection readiness.
  • Operate within AZ policies/SOPs and local regulations.
  • Directly improve the speed, quality, and consistency of AstraZeneca's cell therapy trials-reducing cycle times, elevating protocol adherence, and accelerating patient access to innovative treatments.

You Have:
  • Bachelor's degree in a health-related field required; advanced degree (PharmD, PhD, MSc, NP/PA, MD/RN) is preferred.
  • A minimum of 5 plus years in clinical research or field-facing roles within oncology/hematology or advanced therapies; direct cell therapy experience.
  • Concentrated understanding of GCP, clinical trial operations, and cell therapy patient journey
  • Collaboration and Communication: Excellent partner management ability to translate complex protocols into practical site actions.
  • Ability to travel at least 50-80% regionally/nationally and internationally to support sites and program needs.
  • Patient- and site-centric mindset.
  • Data-informed approach to identify trends, risks, and opportunities for operational improvement.

The annual base pay (or hourly rate of compensation) for this position ranges from $203,709 to $305,564 USD. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.
AstraZeneca offers an environment where you can be empowered to make bold decisions and move at pace. With a focus on Oncology, we are driven by speed and backed by leadership that empowers every level to prioritize smart risks based on scientific evidence. Our scale, agility, and passion ensure fast delivery every time. Join us in pioneering new frontiers in cancer research, where courage, curiosity, and collaboration drive patient outcomes. Be part of a team committed to improving the lives of millions with cancer.
Ready to take on this exciting challenge? Apply now to join our dynamic team.
#LI-Remote
Date Posted
04-Aug-2026
Closing Date
30-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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