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Clinical Data Associate Jobs in Groton, CT (NOW HIRING)

Integrated Resources INC

Bioanalyst

Groton, CT · On-site

$24 - $31.75/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Our client is ... The position involves helping to generate ADME in vitro data through bioanalytical support.

Integrated Resources INC

Chemical Engineer

Groton, CT · On-site

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Support ... Provide experimental support and apply scientific principles, modeling, and lab-scale data-rich ...

Midstate Radiology Associates

MRI Technologist

Mystic, CT · On-site

$49 - $75/hr

Join Midstate Radiology Associates (MRA) as a Full Time, 1st Shift, MRI Technologist to work at our ... Accurately inputs data in the RIS by tracking actual procedure in order to capture all charges and ...

Midstate Radiology Associates

MRI Technologist

Mystic, CT · On-site

$35.50 - $56.48/hr

Join Midstate Radiology Associates (MRA) as a Per Diem, MRI Technologist in our Multiple Locations ... Accurately inputs data in the RIS by tracking actual procedure in order to capture all charges and ...

Midstate Radiology Associates

MRI Technologist

Mystic, CT · On-site

$35.50 - $54.41/hr

Join Midstate Radiology Associates (MRA) as a Full Time, 1st Shift, MRI Technologist to work at our ... Accurately inputs data in the RIS by tracking actual procedure in order to capture all charges and ...

Integrated Resources INC

Bioanalyst

Groton, CT · On-site

$24 - $31.75/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. This is Contract position with my direct client The position involves helping to generate ADME in vitro data ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Groton, CT

Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical data associate in Groton, CT is $38.73, according to ZipRecruiter salary data. Most workers in this role earn between $29.18 and $38.70 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

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What are the most commonly searched types of Clinical Data jobs in Groton, CT?

The most popular types of Clinical Data jobs in Groton, CT are:

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The top searched job categories for Clinical Data Associate jobs in Groton, CT are:

What cities near Groton, CT are hiring for Clinical Data Associate jobs?

Cities near Groton, CT with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Groton, CT as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 19% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $80,564 per year, or $38.7 per hour.

Scientist, Solid-State Characterization

Eurofins

Groton, CT • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 181 frontline employees who took The Breakroom Quiz

64th of 121 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
The Associate Scientist provides laboratory support in synthesizing salt forms and polymorphs of drug candidates and evaluates these forms for acceptability as drug substances with respect to chemical manufacturing and formulation into pharmaceutical products. The successful candidate will engage in solid form characterization and in particle characterization. The position is based in Groton, CT (USA).
Role Responsibilities:
  • Conduct solid state characterization (e.g., X-ray powder diffraction, thermal analysis, moisture sorption, microscopy, spectroscopy) of small molecules of pharmaceutical relevance.
  • Support multidisciplinary project teams and collaborate with colleagues to define and implement crystallization, polymorph, salt, and co-crystal screening activities according to project timelines.
  • Support multidisciplinary project teams and collaborate with colleagues to define and implement API particle characterization activities according to project timelines.
  • Conduct physical and surface characterization of powders of pharmaceutical relevance. This includes particle characterization (e.g., particle size, shape) and surface characterization (e.g., surface energy, surface roughness).
  • Collaborate with colleagues in Medicinal Chemistry, Formulation and Biopharmaceutics to define and implement screening and characterization strategies consistent with solid form selection for clinical studies.
  • Solve scientific problems using contemporary Materials Science experimental techniques.
  • Contribute to the development of new scientific approaches and knowledge within the Materials Science organization.
  • Ensure contemporaneous and accurate entries are made in the electronic laboratory notebook system according to accepted good practice.

Qualifications
  • Bachelor's Degree (BS) with 2+ years of experience or a Master's degree (MS) or a PhD in pharmaceutical science, chemistry, chemical engineering, or related field.
  • Experience in solid state characterization techniques (such as x-ray powder diffraction, polarized light microscopy, differential scanning calorimetry, thermogravimetric analysis, spectroscopy, etc.). Strong data analysis and interpretation skills.
  • Experience and understanding of infrared spectroscopy (FTIR, NIR, FT-Raman) and/or SSNMR is an advantage.
  • Experience with solving Materials Science problems, e.g., solid state chemistry and particle characterization using experimental approaches and team collaboration.
  • Understanding of physical, analytical, and organic chemistry.
  • Good organizational skills, the ability to work independently, and excellent oral and written communication skills are required.
  • A strong interest and motivation to learn new technologies and concepts is expected.
  • Some programming experience is a plus, but not required.

Additional Information
  • The position is full-time, M- F 8 am to 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.
  • 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.

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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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