... management, workforce development, and laboratory operations preferred. * Experience collaborating with oncology, hematopoietic stem cell transplant, and/or clinical trial programs preferred. #LI-EP1 ...
... management, workforce development, and laboratory operations preferred. * Experience collaborating with oncology, hematopoietic stem cell transplant, and/or clinical trial programs preferred. #LI-EP1 ...
Clinical Affairs Scientist
Wilmington, DE · On-site +1
$105K - $197K/yr
The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...
Clinical Affairs Scientist
Wilmington, DE · On-site +1
$105K - $197K/yr
The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...
Study Start-Up Manager
Wilmington, DE · On-site
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Bachelor's degree (higher degree preferred) with knowledge of clinical trial processes (Phases II ...
Study Start-Up Manager
Wilmington, DE · On-site
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Bachelor's degree (higher degree preferred) with knowledge of clinical trial processes (Phases II ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Bachelor's degree (higher degree preferred) with knowledge of clinical trial processes (Phases II ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Bachelor's degree (higher degree preferred) with knowledge of clinical trial processes (Phases II ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Bachelor's degree (higher degree preferred) with knowledge of clinical trial processes (Phases II ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Bachelor's degree (higher degree preferred) with knowledge of clinical trial processes (Phases II ...
Associate Director, Clinical R&D QA US
Wilmington, DE · On-site
$35.50 - $47.25/hr
... Trial Master Files and Clinical submission documents. * Assist with the management of QA ... Be knowledgeable and be able to understand advanced operational, scientific and/or clinical ...
Associate Director, Clinical R&D QA US
Wilmington, DE · On-site
$35.50 - $47.25/hr
... Trial Master Files and Clinical submission documents. * Assist with the management of QA ... Be knowledgeable and be able to understand advanced operational, scientific and/or clinical ...
Associate Director, Clinical R&D QA US
Wilmington, DE · On-site
$35.50 - $47.25/hr
... Trial Master Files and Clinical submission documents. * Assist with the management of QA ... Be knowledgeable and be able to understand advanced operational, scientific and/or clinical ...
Associate Director, Clinical R&D QA US
Wilmington, DE · On-site
$35.50 - $47.25/hr
... Trial Master Files and Clinical submission documents. * Assist with the management of QA ... Be knowledgeable and be able to understand advanced operational, scientific and/or clinical ...
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Quick apply
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Quick apply
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Quick apply
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Quick apply
Operations Manager
Newark, DE · On-site
The Program Manager will support HR, Operations, and the Clinical department as well their respective functions, acting as a reliable source of information to staff, clients, peers, and management.
Study Start Up Manager
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... trial process across Phases II-IV and ICH GCP - Good understanding of clinical protocols and ...
Study Start Up Manager
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... trial process across Phases II-IV and ICH GCP - Good understanding of clinical protocols and ...
Study Start Up Manager
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... trial process across Phases II-IV and ICH GCP - Good understanding of clinical protocols and ...
Study Start Up Manager
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... trial process across Phases II-IV and ICH GCP - Good understanding of clinical protocols and ...
Study Start Up Manager
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... trial process across Phases II-IV and ICH GCP - Good understanding of clinical protocols and ...
Study Start Up Manager
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... trial process across Phases II-IV and ICH GCP - Good understanding of clinical protocols and ...
Clinical Research Technologist II- Biobank
Wilmington, DE · On-site
$55 - $75/hr
This individual will work under the supervision of the Biobank Laboratory Manager and perform ... Additional responsibilities include processing and shipping of clinical trial specimens. Maintains ...
New
Clinical Research Technologist II- Biobank
Wilmington, DE · On-site
$55 - $75/hr
This individual will work under the supervision of the Biobank Laboratory Manager and perform ... Additional responsibilities include processing and shipping of clinical trial specimens. Maintains ...
New
Specialist Study Management
$33.75 - $45.25/hr
Bachelor's degree is preferred * 3-5 years of experience in clinical trial DOCUMENT MANAGEMENT and regulatory documents is required * Operational responsibility to set-up the local Trial Master File ...
Specialist Study Management
$33.75 - $45.25/hr
Bachelor's degree is preferred * 3-5 years of experience in clinical trial DOCUMENT MANAGEMENT and regulatory documents is required * Operational responsibility to set-up the local Trial Master File ...
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required. • Participates in investigator meetings as necessary. Identifies potential ...
Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required. • Participates in investigator meetings as necessary. Identifies potential ...
Clinical Trial Operations Manager information
See Delaware salary details
$28.87 - $35
4% of jobs
$35 - $41.12
6% of jobs
$41.12 - $47.24
7% of jobs
$51.84 is the 25th percentile. Wages below this are outliers.
$47.24 - $53.37
9% of jobs
$53.37 - $59.49
15% of jobs
The median wage is $62.19 / hr.
$59.49 - $65.62
18% of jobs
$69.98 is the 75th percentile. Wages above this are outliers.
$65.62 - $71.74
21% of jobs
$71.74 - $77.86
7% of jobs
$77.86 - $83.99
6% of jobs
$83.99 - $90.11
3% of jobs
$90.11 - $96.24
2% of jobs
$28
$62
$96
How much do clinical trial operations manager jobs pay per hour?
As of Sep 3, 2026, the average hourly pay for clinical trial operations manager in Delaware is $62.57, according to ZipRecruiter salary data. Most workers in this role earn between $50.77 and $70.48 per hour, depending on experience, location, and employer.
What does a clinical trial operations manager do?
A Clinical Trial Operations Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and handle any issues that arise during the trial process. This role is crucial for ensuring that new drugs or medical devices are tested safely and effectively before reaching the market.
What are the key skills and qualifications needed to thrive as a clinical trial operations manager, and why are they important?
To thrive as a Clinical Trial Operations Manager, you need a strong background in clinical research, regulatory compliance, project management, and a relevant degree such as in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Leadership, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These competencies ensure clinical trials are conducted efficiently, ethically, and in accordance with regulatory requirements.
What are some common challenges faced by clinical trial operations managers, and how can they be addressed?
Clinical Trial Operations Managers often encounter challenges such as ensuring regulatory compliance across multiple sites, managing tight timelines, and coordinating diverse teams. Effective communication and proactive planning are essential to address these difficulties. Leveraging project management tools and fostering strong relationships with investigators and site staff can also help streamline operations and reduce risks of delays or protocol deviations.
What is the difference between Clinical Trial Operations Manager vs Clinical Research Coordinator?
| Aspect | Clinical Trial Operations Manager | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree; often advanced degrees or certifications in clinical research or management | Bachelor's degree in health sciences or related field; certifications like CCRP are common |
| Work Environment | Oversees multiple trials, manages teams, and coordinates with stakeholders in clinical settings | Works directly with participants, manages trial documentation, and supports daily trial activities |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Clinical Trial Operations Manager focuses on overseeing entire clinical trial processes, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at the trial site, working closely with participants and supporting trial documentation. Both roles require relevant certifications and are essential in the clinical research industry, but they differ in scope and responsibilities.
What are the most commonly searched types of Clinical Trial Operations jobs in Delaware?
The most popular types of Clinical Trial Operations jobs in Delaware are:
What cities in Delaware are hiring for Clinical Trial Operations Manager jobs?
Cities in Delaware with the most Clinical Trial Operations Manager job openings:
Full-time
Posted 7 days ago
Nemours Children's Health rating
8.1
Based on 87 frontline employees who took The Breakroom Quiz
67th of 898 rated healthcare providers
Job description
Nemours Children's Health is seeking a Supervisor, Laboratory Operations for the Hematopathology service to provide technical, operational, quality, and people leadership. This role supports safe, reliable daily operations for pediatric oncology, hematopoietic stem cell transplant, and clinical trial services in partnership with laboratory administration, medical leadership, and clinical stakeholders.
Work Schedule: Monday - Friday, 9a-5p with an On Call weekend rotation.
The Supervisor, Laboratory Operations oversees standardized workflows, high-complexity testing, quality assurance, regulatory readiness, workforce development, fiscal stewardship, and continuous improvement. The position serves as an operational bridge between laboratory services and clinical partners, ensuring accurate, timely, and clinically meaningful results while advancing Nemours Children's Health and departmental goals.
Essential Responsibilities
- Provide day-to-day operational oversight for high complexity hematopathology testing, including bone marrow morphology and flow cytometry.
- Ensure testing is performed accurately, safely, compliant with all regulatory requirements. Ensures within established turnaround times, with appropriate corrective action and follow-up when needed.
- Partner with medical, laboratory, and administrative leaders to evaluate, validate, implement, and monitor new assays, methods, instruments, software, and workflows.
- Serve as a technical and operational resource for laboratory staff, physicians, clinical teams, and organizational partners.
- Act as an operational liaison to oncology, hematopoietic stem cell transplant, clinical trials, pathology, and other clinical stakeholders.
- Maintain continuous readiness for licensing, accreditation, and regulatory inspections and coordinate timely correction of identified deficiencies.
- Establish and monitor quality control, proficiency testing, quality assurance, quality improvement activities, and laboratory performance indicators. Completes the necessary investigation and follows through with all corrective and preventive actions.
- Lead, coach, schedule, develop, and evaluate assigned technical and non-technical personnel while promoting a safe, respectful, inclusive, and collaborative work environment.
- Support operating and capital budget activities, purchasing, staffing, inventory, equipment, workload statistics, and operational records.
- Evaluate laboratory information system and informatics processes, support workflow validation, ensure staff training, and maintain complete and secure documentation.
Ideal Candidate
The ideal candidate is an experienced clinical laboratory professional and people leader with expertise in hematology, flow cytometry, bone marrow morphology, quality management, regulatory readiness, and laboratory operations. This individual communicates effectively with interdisciplinary partners, applies sound judgment in complex operational settings, and is committed to patient safety, staff development, operational excellence, and continuous improvement.
Job Requirements
- B. S. in Medical Technology (B.S.M.T. or equivalent, e.g., HHS examination or ability to meet CLIA qualifications for Moderate complexity laboratory testing) required.
- Minimum five (5) years of practical clinical laboratory experience, including instrumentation and high-complexity testing.
- Minimum three (3) years of experience as a supervisor or team lead, or an equivalent combination of leadership experience consistent with organizational requirements.
- Nationally/Internationally recognized certification as a Medical Laboratory Scientist or equivalent (ASCP, AAB, or AMT) eligible. Must obtain within 6 months of hire date.
- Flow cytometry and/or hematology experience strongly preferred; experience with bone marrow morphology or hematologic malignancy diagnostics preferred.
- Experience supporting assay validation, regulatory inspections, quality management, workforce development, and laboratory operations preferred.
- Experience collaborating with oncology, hematopoietic stem cell transplant, and/or clinical trial programs preferred.
#LI-EP1
About Us
Nemours Children's Health is an internationally recognized pediatric health system serving more than 1.7 million patient encounters each year. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Backed by the Nemours Foundation and Alfred I. duPont Trust, our $1.7B nonprofit system is dedicated to improving children's health through clinical care, research, education, advocacy, and prevention. Our Whole Child Health approach focuses equally on prevention and treatment, partnering with communities to help every child thrive.
Inclusion and belonging guide our strategy and growth. We are committed to culturally relevant care, reducing health disparities, and fostering an environment where every associate, patient, and family feels supported and valued.
Learn more at Nemours.org.
What Nemours Children's Health employees say
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Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Nemours
Sourced by ZipRecruiter
As one of the nation's leading pediatric health care systems, Nemours is committed to providing all children with their best chance to grow up healthy. We offer integrated, family-centered care to more than 300,000 children each year in our pediatric hospitals, specialty clinics, primary care practices, and school-based health centers in Delaware, Florida, Maryland, New Jersey and Pennsylvania. Nemours strives to ensure a healthier tomorrow for all children - even those who may never enter our doors - through our world-changing research, education and advocacy efforts.
Industry
Health care and social assistance and hospitals
Company size
1,001 - 5,000 Employees
Headquarters location
Jacksonville, FL, US