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Clinical Study Associate Jobs in Connecticut (NOW HIRING)

Eurofins

Associate Materials Scientist

Groton, CT · On-site

... clinical studies, as well as having an emerging global presence in Contract Development and ... The Associate Scientist provides laboratory support in synthesizing salt forms and polymorphs of ...

Ki Health Partners

Clinical Research Assistant

Monroe, CT · On-site

$18 - $23/hr

Ki Health Partners, LLC, is looking for a motivated Clinical Research Associate to assist in ... studies, and over 90% of our research endeavors have resulted in the approval by the Food and Drug ...

Ki Health Partners

Clinical Research Assistant

Monroe, CT · On-site

$18 - $23/hr

Ki Health Partners, LLC, is looking for a motivated Clinical Research Associate to assist in ... studies, and over 90% of our research endeavors have resulted in the approval by the Food and Drug ...

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Clinical Study Associate information

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How much do clinical study associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical study associate in Connecticut is $30.00, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $39.57 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 Connecticut?

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

What cities in Connecticut are hiring for Clinical Study Associate jobs?

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

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 25% Part Time, 3% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $62,408 per year, or $30 per hour.

Associate Scientist, Formulation Development

Eurofins

Groton, CT • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

68th of 120 rated laboratories

Job description

Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
  • Preparation of prototype formulations (solutions, suspensions, tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids) for exploratory studies in in-vitro and in-vivo models
  • Development of oral, topical and intravenous (sterile) dosage forms for feasibility studies and small scale manufacturing operations
  • Measurement of key active compound and formulation properties (such as solubility, tablet hardness, disintegration, pH, isotonicity, color, gelling tendency, etc.)
  • Assessment of the chemical and physical stability of prototype formulations, as well as the performance of prototype formulations using in-vitro tests (non-sink dissolution, precipitation, etc.)
  • Identify potential stability and performance issues with prototype formulations
  • Development of protocols for preparation of formulations at preclinical and clinical study sites

Qualifications
The Ideal Candidate would possess:
  • Experience with drug formulation and pre-formulation techniques, and an understanding of drug candidate properties
  • Experience with amorphous solid dispersions (spray dried dispersions or hot melt extrusion) and modified release tablet design.
  • Basic chemistry (wet or solid state) laboratory experience.
  • Experience working with laboratory equipment, mechanically inclined.
  • Experience with more advanced characterization techniques such as Raman, thermal analysis and dissolution.
  • Ability to follow procedures reliably and consistently,
  • Strong computer and organizational skills
  • Adept in Microsoft office
  • Mathematical or Mechanistic Modeling
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivated, adaptable, and a positive attitude
  • Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies

Additional Information
  • The position is full-time, Monday through Friday, 8am-5 pm
  • May be requested to work on weekends, overtime, and holidays based on business needs.
  • Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
  • Ability to work overtime as required.
  • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • #LI-EB1

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

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Hours and flexibility

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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