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Clinical Study Associate Jobs in Delaware (NOW HIRING)

BluePearl is proud to offer our full-time associates : * 401(k) with employer match . * Health ... BluePearl Science - participate and learn from ongoing clinical studies at BluePearl. * BluePearl ...

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Clinical Study Associate information

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$12

$31

$55

How much do clinical study associate jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical study associate in Delaware is $31.57, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.63 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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 cities in Delaware are hiring for Clinical Study Associate jobs?

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

Infographic showing various Clinical Study 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 $65,660 per year, or $31.6 per hour.

Associate Investigator Grant Analyst

Thermo Fisher Scientific

Wilmington, DE

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

200th of 540 rated manufacturers


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Job Description

Join Us as an Associate Investigator Grant Analyst - Make an Impact at the Forefront of Innovation.


The Associate Investigator Grant Analyst (AIGA) prepares, reviews and finalizes global investigator grant budget and payment schedule terms and conditions templates for multiple studies. The role involves developing investigator grant budget negotiation parameters with clients, communicating client processes, procedures and negotiating parameters to local team members. The Associate Investigator Grant Analyst liaises and establishes effective relationships with clients and internal functional teams and Contract Specialists as directed by Contract Managers.

This is a fully remote opportunity for candidates located in the United States. Sponsorship is not provided for this role.
Essential Functions:
• Assist in the development of investigator grant budget grids for applicable countries in assigned studies inclusive of coordination with therapeutic and operational subject matter experts, as appropriate, to ensure proper grant development.
• Draft applicable payment terms and condition templates for investigator grant budget grids.
• Coordinate internal/external approvals and feedback to investigator grant budget grids and payment schedules.
• Provide support for escalations with external clients for investigator budget development, process and negotiation parameters.
• Provide approved investigator grant grids and payment schedules, process and negotiation parameters to local teams.
• Coordinate with internal departments to ensure various site startup activities are aligned with investigator grant activities and mutually agreed upon timelines; ensure alignment of investigator budget negotiation process for sites and study are properly aligned to the critical path for site activation.
• Adhere to company’s target cycle times for site activations.
• Complete tracking and reporting as required.
Education & Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities:
• Basic understanding of the principles of investigator grant template drafting
• Capable of reviewing and analyzing a protocol schedule of events to draft applicable budget grid and payment schedules therefrom
• Basic understanding of the pharmaceutical product development process and involvement of CROs
• Good oral and written communication skills
• Good attention to detail
• Good math skills
• Capable of working independently or in a team environment
• Good organizational and time management skills
• Proven flexibility and adaptability
• Basic proficiency with negotiation and conflict management
• Possesses cross cultural awareness and is able to adapt appropriately
• Good customer service skills, demonstrating a customer focused style of communication, problem solving and collaboration
• Basic experience with automated systems and computerized applications, such as, Microsoft Outlook, Excel, Word, etc
• Capable of acting independently and leading functional studies with general oversight.
Working Conditions and Environment:
• Work is performed in an office/ laboratory and/or a clinical environment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Exposure to electrical office equipment.
• Personal protective equipment required such as protective eyewear, garments and gloves.

Salary Transparency:

This is a salaried role that will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. Compensation will be initially discussed during the screening period, with actual compensation confirmed in writing at the time of offer.

We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally include:

• A choice of national medical and dental plans, and a national vision plan

• A wellness program, and valuable health incentive opportunities for company contributions to a Health Reimbursement Accounts (HSAs) or Health Savings Account (HSA)

•Tax-advantaged savings and spending accounts and commuter benefits

• Employee assistance programs

• At least 120 hours paid time off (PTO). 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer rime off in accordance with company policy.

• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan


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