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Contract Clinical Research Associate Jobs in Delaware

Chattyvets

Veterinarian

Newark, DE · On-site

$90 - $130/hr

Associate Veterinarian - Newark, DE | AAHA Accredited | New Graduates Welcome | Sign-On Bonus ... Access to clinical research opportunities * Mental health and wellbeing support * Financial ...

QPS, LLC

Associate Scientist I - TLM

Newark, DE · On-site

$45K - $50K/yr

... IV Clinical Research services. To meet the needs of our clients, we strive to employ talented ... Associate's Degree plus 2 or more years relevant experience * Desire to learn and grow ...

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All JobsContract Clinical Research Associate JobsContract Clinical Research Associate Jobs in Delaware

Contract Clinical Research Associate information

See Delaware salary details

$12

$41

$69

How much do contract clinical research associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for contract clinical research associate in Delaware is $41.16, according to ZipRecruiter salary data. Most workers in this role earn between $28.89 and $52.69 per hour, depending on experience, location, and employer.

What is a contract clinical research associate?

Contract Clinical Research Associates (CRAs) are professionals who monitor clinical trials on behalf of pharmaceutical companies, contract research organizations (CROs), or other sponsors, but work on a contract or freelance basis rather than as permanent employees. Their primary responsibilities include ensuring that trials are conducted according to regulatory guidelines, monitoring data accuracy, and verifying that patient rights and safety are protected. Contract CRAs may work on multiple projects for different clients and often enjoy more flexibility in their schedules and work locations. This role requires strong organizational skills, knowledge of Good Clinical Practice (GCP), and the ability to travel to clinical sites.

What are some of the unique challenges faced by contract clinical research associates compared to permanent employees?

Contract Clinical Research Associates often need to quickly adapt to new study protocols, sponsor requirements, and team dynamics since they may work on multiple projects for different organizations. This can mean a faster onboarding process and the need to build rapport with new colleagues and site staff efficiently. Additionally, contract CRAs must be highly organized to manage shifting assignments and maintain compliance across different trial sites, as well as keep up with varying documentation standards. While this variety can be rewarding, it can also present challenges in terms of consistency and long-term project ownership.

What are the key skills and qualifications needed to thrive as a contract clinical research associate, and why are they important?

To thrive as a Contract Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and ICH), and typically a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong attention to detail, organizational skills, and effective communication help build productive site relationships and ensure compliance. These skills are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting successful clinical trial outcomes.

What is the difference between Contract Clinical Research Associate vs Clinical Research Associate?

AspectContract Clinical Research AssociateClinical Research Associate
CredentialsTypically requires a degree in life sciences and relevant certificationsSame as Contract CRA, often with additional experience
Work EnvironmentTemporary, project-based assignments often with multiple sponsorsFull-time employment with a single organization or sponsor
Employer & Industry UsageUsed by CROs and pharma companies for short-term projectsCommonly employed directly by pharmaceutical companies or CROs
Search & Comparison IntentOften compared for flexibility and contract work benefitsViewed as a permanent role with career growth

In summary, Contract Clinical Research Associates work on temporary, project-specific basis, often with multiple sponsors, offering flexibility. Clinical Research Associates typically hold full-time roles within a single organization, providing stability and career development opportunities.

What are popular job titles related to Contract Clinical Research Associate jobs in Delaware?

For Contract Clinical Research Associate jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Contract Clinical Research Associate jobs in Delaware look for?

The top searched job categories for Contract Clinical Research Associate jobs in Delaware are:

What cities in Delaware are hiring for Contract Clinical Research Associate jobs?

Cities in Delaware with the most Contract Clinical Research Associate job openings:

Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research Associate job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $85,616 per year, or $41.2 per hour.

FSP Associate Scientist

Thermo Fisher Scientific

Wilmington, DE • On-site

Full-time

Posted 5 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

175th of 544 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Location/Division Specific Information
Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our clients to make the world healthier, safer, and cleaner.
Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. This is an onsite position located in Wilmington, DE
A Day in the life:
  • Perform or aid in purification process development, optimization, and scale-up manufacturing
  • Conduct protein purification to support formulation team's material needs and cell culture development
  • Perform routine analyses of in-process samples using relevant product purity and process impurity analytical tools
  • Prepare buffers and solutions needed for laboratory work
  • Present work summary in a weekly group meeting
  • Write routine electronic laboratory notebook entries
  • Other responsibilities as assigned

Knowledge, Skills & Abilities
  • Basic knowledge in protein chemistry and bioprocessing
  • Basic knowledge and preferably hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology
  • Experience in protein analysis such as HPLC, ELISA, pH/Conductivity/A280 Concentration testing, etc. is preferred
  • Hands-on experience or basic knowledge of Ultrafiltration/Diafiltration experimentation and TFF systems is preferred
  • Inventory management skills preferred
  • Good verbal and written communication skills
  • Organized, collaborative, independent, meticulous

Education and Experience:
  • Bachelor's degree in in Chemical Engineering, Biomedical Engineering, or Biological Sciences, or other related degree concentration, or equivalent directly-related experience
  • 0-2 years of directly related industry experience is equivalent to one full-time year of college in related major)
  • Ability to work weekends and overnight hours as needed
In some cases an equivalency, consisting of appropriate education, training, and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Our 4i Values:
Integrity - Innovation - Intensity - Involvement
If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, submit your application - we'd love to hear from you!

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