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Contract Patient Reported Outcome Jobs in Delaware

Contract Analyst

Wilmington, DE · On-site

$68K - $109K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... health outcomes, making high-quality care more accessible, and lowering healthcare costs ... News & World Report as the Best Hospital. With the unique CareVio data-powered care coordination ...

$20/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

This includes providing information and reports to client contact(s), keeping them current on our ... Other Duties as assigned or required by client contract Additional Duties and Responsibilities:

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

This includes providing information and reports to client contact(s), keeping them current on our ... Other Duties as assigned or required by client contract Additional Duties and Responsibilities:

PCT / PATIENT CARE TECH - CARDIAC

Lewes, DE · On-site

$17.25 - $26.74/hr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Monitor and record vital signs, intake and output, and other patient data, reporting any ... patient outcomes * Completes hourly rounds to assigned patients and anticipates patient needs.

PCT / PATIENT CARE TECH - CARDIAC

Lewes, DE · On-site

$17.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Monitor and record vital signs, intake and output, and other patient data, reporting any ... patient outcomes * Completes hourly rounds to assigned patients and anticipates patient needs.

Local Contract Title: Speech Language Pathologist Length of assignment: 21 Weeks Shift: 08:00 AM ... identifies, and reports the need for repair of equipment, as necessary. * Puts Patient Service ...

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Contract Patient Reported Outcome information

What is the difference between Contract Patient Reported Outcome vs Contract Data Coordinator?

AspectContract Patient Reported OutcomeContract Data Coordinator
CredentialsTypically requires clinical research or healthcare certifications, familiarity with patient-reported dataRequires data management, database, or clinical research certifications
Work EnvironmentHealthcare settings, clinical research sites, or remote patient data collectionResearch organizations, clinical trial sites, or data management teams
Industry UsageUsed in clinical trials to gather patient feedback on treatmentsUsed to organize, validate, and manage research data

Contract Patient Reported Outcome roles focus on collecting and analyzing patient feedback in clinical trials, while Contract Data Coordinators handle the organization and validation of research data. Both roles are essential in clinical research but serve different functions within the data collection and management process.

What are popular job titles related to Contract Patient Reported Outcome jobs in Delaware?

For Contract Patient Reported Outcome jobs in Delaware, the most frequently searched job titles are:

What cities in Delaware are hiring for Contract Patient Reported Outcome jobs?

Cities in Delaware with the most Contract Patient Reported Outcome job openings:

Infographic showing various Contract Patient Reported Outcome job openings in Delaware as of August 2026, with employment types broken down into 3% As Needed, 70% Full Time, 19% Part Time, and 8% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

US Medical Head, Dyslipidemia

AstraZeneca

Wilmington, DE

Full-time

Re-posted 13 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

At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's exceptional skills with those of people from all over the globe. AstraZeneca holds an outstanding position in CVRM disease, with a range of medicines both on the market and in development, with an industry leading pipeline.

TheUS Head of Medical - Dyslipidemiais a leadership position that reports directly to the VP Medical Cardiovascular Renal Metabolism (CVRM), within the BioPharmaceuticals Business Unit's US Medical CVRM franchise. The successful candidate will lead a team to develop product and disease area strategies and drive product launches for our novel Aldosterone Synthase Inhibitor (ASI) across the life-cycle.

What you'll do:
  • Build and lead the dyslipidemia medical team, with accountability for the development and execution of disease area and brand strategies and plans
  • Accountable for disease area and brand budget and resource requirements
  • Partner effectively with the Commercial Lead, role-modeling effective teamwork across the enterprise
  • Effectively act as the US point of contact for the Global Product Team (GPT)
  • Provide the US viewpoint into life-cycle management/phase IV strategy and study design
  • Develop and maintain positive relationships with key external and internal customers
  • Anticipate future trends and needs in the marketplace
  • Coach, mentor and performance lead direct reports and take an active role in succession and talent management
  • Develop and foster a team culture that encourages continued growth and recognition
  • Collaborate and build internal and external networks
  • Deliver results in a sophisticated matrix environment, building capabilities, and leading large scale impactful medical initiatives
  • Lead the of launch of new products
  • Leverage AI and digital driven analytics, platforms and clinical solutions to improve medical planning, scientific engagement, evidence generation and patient outcomes
  • Ensure compliance with all AZ corporate policies
Requirements for the role:
  • Sophisticated Scientific Degree (MBBS, PharmD, PhD, or MD) or equivalent education
  • A minimum of 7 years of experience in the pharmaceutical industry, ideally in Medical Affairs and in the dyslipidemia space
  • A minimum of 5 years of experience leading high performing teams in the pharmaceutical industry
  • Medical/clinical/scientific expertise in CVRM
  • US Regulatory Strategy Knowledge/Experience, including new product approval, labeling requirements/negotiations
  • Strong business acumen, with comprehensive understanding of the U.S. healthcare environment
Desirable Skills/Experience
  • Phase 3b/4 and post-approval dedication research including leading all aspects of patient registries and REMS programs
  • Translational medicine, population-based real-world research
  • Bridging with coordinated care management & Quality improvement pathways
  • Understanding of Health Outcomes Research including Patient-reported outcomes
  • Experience integrating emerging technologies-such as AIsupported insights, machine learning tools, or digital medical platforms-into medical affairs strategies or operational processes.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Join our globally renowned CVRM team. It's an exciting time to join as we work towards our big ambitions with entrepreneurial thinking and innovation. It's up to us to find solutions and act fast to make them happen.

Ready to make a difference? Apply today!

Date Posted

11-Aug-2026

Closing Date

25-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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