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Compound Management Jobs in Delaware (NOW HIRING)

Qnity

Manufacturing Development Engineer

Newark, DE

This work includes running tests and analyzing results on compound physical properties, chemical ... Ability to manage and lead both strategic long-term programs/projects, as well as address short ...

Four Seasons

Welcome and seat guests promptly while managing reservations and table assignments. * Ensure ... Full board shared living accommodation in a high quality, well-resourced compound * Complimentary ...

Four Seasons

$19 - $24/hr

Manage recipe costing, create pickup charts, and develop spreadsheets to enhance efficiency ... Complimentary shared accommodation on full board basis in a high quality, well-resourced compound ...

Four Seasons

$13.50 - $16.50/hr

Reports any problems or deficiencies to manager. * Complies with Four Seasons' Category One and ... Full board shared living accommodation in a high quality, well-resourced compound * Complimentary ...

Four Seasons

Report any complaints to the management team. * Upsell Spa products considering guests' needs and ... Full board shared living accommodation in a high quality, well-resourced compound * Complimentary ...

Harris Teeter

PRN Part Time Hourly Pharmacist

Selbyville, DE · On-site

$56.75 - $68.25/hr

Dispense or compound medications to customers pursuant to prescriptions - following laws ... Communicate with management about advertising, merchandising and any errors seen affecting customer ...

Four Seasons

$19 - $24/hr

Control food costs and manage inventory effectively through organized purchasing, portion control ... Complimentary full-board single accommodation in a high-quality, well-resourced compound with Wi-Fi ...

Four Seasons

$19 - $24/hr

Control food costs and manage inventory effectively through organized purchasing, portion control ... Complimentary full-board sharing accommodation in a high-quality, well-resourced compound with ...

Merck & Co.

$19.25 - $24.25/hr

... compound containment. - - Instrumentation Lifecycle Management - Accountable for QC instrumentation strategy, selection, procurement, and delivery planning across all analytical platforms (HPLC/UPLC ...

Four Seasons

$16 - $20/hr

Strong organization and time management skills. * Ability to work under pressure. What we offer * Full-board shared living accommodation in a high-quality, well-resourced compound * Complimentary ...

All JobsCompound Management JobsCompound Management Jobs in Delaware

Compound Management information

See Delaware salary details

$12

$22

$34

How much do compound management jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for compound management in Delaware is $22.55, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $24.28 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Compound Management position, and why are they important?

To thrive in Compound Management, you need a solid background in laboratory sciences, attention to detail, and experience handling chemical compounds, often backed by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), inventory tracking software, and best practices for safe handling and storage of substances is highly beneficial. Strong organizational, problem-solving, and communication skills are essential for managing inventory, coordinating with research teams, and addressing logistical challenges. These skills are critical to ensuring compound integrity, supporting scientific workflows, and maintaining safety and efficiency in research environments.

What are the typical daily responsibilities for someone working in Compound Management?

Professionals in Compound Management are responsible for receiving, cataloging, storing, and distributing chemical or biological samples within research or pharmaceutical environments. On a daily basis, you may prepare compounds for experiments, manage inventory records, conduct quality checks, and coordinate with scientists to fulfill project requests. Ensuring proper documentation, compliance with safety standards, and maintaining the integrity of compounds are central to the role. Working closely with researchers and laboratory staff is common, making teamwork and timely communication essential for success.

What is a Compound Management job?

A Compound Management job involves overseeing the storage, tracking, and distribution of chemical compounds in a laboratory or research setting. Professionals in this role ensure that samples are properly organized, labeled, and made available for researchers while maintaining database accuracy and compliance with safety regulations. They may also be responsible for inventory management, automation, and quality control to support drug discovery and development.

What are popular job titles related to Compound Management jobs in Delaware? For Compound Management jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Compound Management jobs in Delaware look for? The top searched job categories for Compound Management jobs in Delaware are:
What cities in Delaware are hiring for Compound Management jobs? Cities in Delaware with the most Compound Management job openings:
Compound Management jobs near you
Infographic showing various Compound Management job openings in Delaware as of July 2026, with employment types broken down into 21% Locum Tenens, 66% Full Time, 8% Part Time, 2% Contract, 1% Nights, and 2% Summer. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $46,904 per year, or $22.6 per hour.
Senior Director, Clinical Operations

Senior Director, Clinical Operations

Incyte Corporation

Wilmington, DE • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

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 Senior Director, Clinical Operations is responsible for providing strategic planning, tactical implementation, and reporting of clinical investigations involving human subjects. The position would be responsible for management of clinical studies to ensure compliance with corporate objectives, regulatory requirements and appropriate guidance, direction of clinical operations personnel, contract research organizations, consultants, core laboratories, and all other study support organizations for assigned clinical trials. The workload of direct trial responsible may depend on the workload and complexity of the trials. This position is also responsible for program level activities as assigned. Finally, this position is accountable for the day-to day clinical development operational plans in accordance with budget and timelines and with standard operating procedures (SOP), ICH Good Clinical Practices and any other specific country regulations.
Essential Functions of the Job (Key responsibilities)
  • Provide clear objectives, ongoing feedback and end of performance review for direct reports.
  • Maintain and develop Investigator sites and KOLs relationship.
  • Maintaining close collaboration with clinical development, other internal departments and external vendors.
  • Contribute to the hiring plan and staffing activities including efficient on-boarding, training and mentoring of new employees.
  • Clinical Trial Managers and Clinical Trial Specialists to resource the studies across the compound. Provides updates and status reports to Sr. Management, as requested.
  • Contribute to the hiring plan and staffing activities including efficient on-boarding, training and mentoring of new employees.
  • Align the Clinical Trial Heads.
  • Assist for clinical program/trials implementation including operational feasibility, resource forecast and management across the compound.
  • Collaborates with Sr. Management to determine clinical supply requirements for clinical trials/program.
  • Participate in the strategy, design, development and review of clinical trial protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research related documents and study reports; participate as required in the preparation of the clinical contribution to IND's, Investigational Brochure, regulatory Briefing Documents, and other relevant documentation.
  • Plans, implements and manages, in collaboration with CRO partners, Phase I-III clinical trials, as necessary.
  • Collaborates with Sr. Management, internal project team and CRO partners, as applicable, to prepare clinical trials/program timelines, budget and key deliverables consistent with departmental and corporate objectives.
  • Assists in the preparation of 'Requests for Proposal' documents and financial analysis of CRO proposal costs and negotiation.
  • Assists in the strategic oversight of the Clinical Research Organization (CRO) and other vendors.
  • Assists in the development and writing of clinical Trials/program documents and manuals as appropriate.
  • Accountable for development and execution of accurate operational Development plans, including assuring harmonization and high data quality across clinical trials/program.

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Bachelor of Science degree or a degree in a field relevant to a profession in biopharmaceutical industry.
  • Minimum of 8 years of experience working in project management and/or clinical operations within the biopharmaceutical industries and/or Clinical Research Organization ('CRO') and at least 3 years in a role of primary clinical trial design, execution and management required.
  • Good knowledge of GCPs, clinical trial design, statistics, regulatory processes, and drug development process
  • Proven ability to lead multi-disciplinary teams.
  • Must have the ability to develop and administer budgets, schedules and performance requirements, direct resources effectively, meet company objectives, provide technical advice and assist with problem resolution and work well under pressure.
  • Experience in developing effective relationships with key investigators.
  • Must have experience in appropriate therapeutic area; preference in Oncology.
  • Experience in program management preferred.
  • Operational and direct managerial experience in the planning, executing and reporting of global clinical development trials.
  • Must be able to travel (domestic and international) up to 10%.

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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