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Clinical Study Manager Jobs in Delaware (NOW HIRING)

Straumann

Territory Manager - Delaware

Wilmington, DE · On-site

As a Territory Manager, you will embody our core values of collaboration, agility, ownership, and ... Stay informed about key clinical studies and scientific papers supporting Straumann's product ...

Protouch Staffing

Endocrinologist

Lewes, DE · On-site

$260K - $320K/yr

Interpret endocrine laboratory results, imaging, and diagnostic studies * Manage insulin pumps ... Strong outpatient endocrine clinical skills * Interest in obesity medicine and preventive metabolic ...

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Clinical Study Manager information

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$62

$96

How much do clinical study manager jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical study 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 are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

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

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

What are popular job titles related to Clinical Study Manager jobs in Delaware?

For Clinical Study Manager jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Delaware look for?

The top searched job categories for Clinical Study Manager jobs in Delaware are:

What cities in Delaware are hiring for Clinical Study Manager jobs?

Cities in Delaware with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Delaware as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $130,146 per year, or $62.6 per hour.

Medical Science Liaison, Rare Hematology, Pacific Northwest (WA, OR, ID, MT, AK)

AstraZeneca

Wilmington, DE • On-site

Full-time

Re-posted 10 days ago

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

This is what you will do:
The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion, AstraZeneca Rare Disease's product/s across the product/s life cycle. The individual is a peer scientific expert who communicates accurate and applicable science to Healthcare Practitioners (HCPs) within a geographic area. The individual manages and maintains collegial and professional relationships with HCPs and Key Opinion Leaders (KOLs) and identifies and facilitates collaboration opportunities with Alexion, AstraZeneca Rare Disease. The MSL combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally to Medical Directors, USMA Leadership Team, cross-functional partners and externally (HCPs & KOLs). The MSL should be able to identify problems early on, seek appropriate help and counsel to work past any barriers, and innovate in order to achieve medical goals and objectives.
You will be responsible for:
HCP relationship management
  • Evaluates their territory to profile and identify the HCPs to engage and build relationships with, as well as identify, important centers of excellence
  • Develops clear, succinct, impactful HCP engagement plans, aligned with medical strategic goals and objectives. Evaluates and refines plans as needed per the progress against the quarterly focus priorities
  • Gains HCPs' trust and respect by effectively providing and communicating relevant scientific/medical information on the company's products and disease states
  • Gathers and disseminates HCP insights as appropriate internally to help inform medical strategy
  • Develops strong working relationships in different external business settings

Scientific knowledge and training
  • Keeps current with scientific knowledge within assigned products and therapeutic area
  • Supports scientific exchange of product/disease state with external stakeholders (HCPs) as needed
  • Provides relevant scientific information to other internal teams and functions as appropriate
  • Demonstrates a functional understanding of real-world evidence and HEOR

Research & Development
  • Demonstrates a strong understanding of clinical study design and protocols
  • Ensures HCPs and stakeholders receive focused and balanced clinical and scientific information
  • Develops expertise in applicable research outcomes to credibly conduct effective discussion with HCPs
  • Supports applicable externally sponsored research and clinical trials, as appropriate

US Healthcare system knowledge
  • Acquires knowledge of the current US healthcare system environment and its impact on the rare disease ecosystem
  • Builds a basic understanding of the foundations of managed markets
  • Acquires a basic understanding of the flow of information in managed care and government organizations

You will need to have:
Minimum Education
  • MD, PharmD, or PhD in biological sciences strongly preferred
  • Clinical experience in a relevant therapeutic area OR track record of success as an MSL

Minimum Experience
  • Industry experience is preferred but not mandatory; if no industry experience, therapeutic area experience (Hematology/Nephrology/Transplant) is preferred

Specific Knowledge, Skills, and Abilities
  • Has excellent communication skills (oral and written)
  • Energetically embraces responsibilities and demonstrates the ability to achieve goals
  • Has a strong personal initiative
  • Functions well as part of a cross-functional team
  • Exhibits excellent time management
  • Able to work independently
  • Demonstrates leadership skills and high-level job competencies

Additional Role Requirements
  • Office is home based. Travel within region 3-4 days per week with 1-2 office days per week
  • Person should be able to travel minimum ~70% time
  • Required travel to medical meetings, team meetings and other group meetings (including possible weekends, as dictated by conference schedule)
  • Candidate is required to live within the territory
  • The duties of this role are generally conducted in a field environment. As is typical of a field-based role, employees must be able, with or without an accommodation, to travel by public transportation, automobile, train, or plane; work comfortably in a clinical setting; use a computer; engage in communications via phone, video, and electronic messaging; problem solve; engage in complex and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours
  • At AstraZeneca, we are taking bold action on climate because we recognize the connection between healthy people and a healthy planet. As part of our flagship Ambition Zero Carbon program, we have committed to a fully electric vehicle (EV) fleet by the end of 2025, which means that all of our drivers will be assigned an EV. Ability to travel within territory on a regular basis which will include frequent overnight and weekend travel. Valid driver's license and clean driving record required).
  • All activities should be conducted per Alexion, AstraZeneca Rare Disease policies.

Date Posted
10-Aug-2026
Closing Date
23-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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