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Clinical Research Associate Jobs in Rindge, NH (NOW HIRING)

Eurofins

EMC/Wireless Engineer - 2nd Shift

Littleton, MA · On-site

$70K - $100K/yr

... Research Organisation services. Eurofins is one of the market leaders in certain testing and ... The Group also has a rapidly developing presence in highly specialised and molecular clinical ...

Eurofins

EMC/Wireless Engineer

Littleton, MA · On-site

$70K - $100K/yr

... Research Organisation services. Eurofins is one of the market leaders in certain testing and ... The Group also has a rapidly developing presence in highly specialised and molecular clinical ...

Eurofins Scientific

EMC/Wireless Engineer

Littleton, MA · On-site

$70K - $100K/yr

... Research Organisation services. Eurofins is one of the market leaders in certain testing and ... The Group also has a rapidly developing presence in highly specialised and molecular clinical ...

Umass Memorial Health

PCT I/II, Per Diem

Clinton, MA

Exceptional patient care, academic excellence and leading-edge research make UMass Memorial the ... Under the direction of the appropriate licensed clinician, the Patient Care Technician I performs a ...

UMass Memorial Health

PCT I/II, Per Diem

Clinton, MA · On-site

Exceptional patient care, academic excellence and leading-edge research make UMass Memorial the ... Under the direction of the appropriate licensed clinician, the Patient Care Technician I performs a ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Rindge, NH

Clinical Research Associate information

See Rindge, NH salary details

$11

$40

$68

How much do clinical research associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for clinical research associate in Rindge, NH is $40.42, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $51.73 per hour, depending on experience, location, and employer.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry may be challenging for those without related experience or training.

What are Clinical Research Associates?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate jobs
What cities near Rindge, NH are hiring for Clinical Research Associate jobs? Cities near Rindge, NH with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Rindge, NH as of June 2026, with employment types broken down into 67% Full Time, 30% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $84,071 per year, or $40.4 per hour.

EMC/Wireless Engineer

Eurofins USA Consumer Product Testing

Littleton, MA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

Job Summary: The EMC/WIR Engineer is responsible for conducting tests to evaluate the electromagnetic compatibility (EMC) and electromagnetic interference (EMI) of various electronic devices and systems. This role involves setting up and operating testing equipment, analyzing test results, and ensuring compliance with industry standards and regulations.

Key Responsibilities:

  • Test Preparation and Setup: Prepare and set up EMC testing equipment and test environments according to specified procedures and standards.
  • Conducting Tests: Perform EMC and EMI tests on electronic devices and systems to identify potential interference issues.
  • Data Analysis: Analyze test data to determine the level of electromagnetic interference and compatibility of the tested devices.
  • Reporting: Document and report test results, including any identified issues and recommended corrective actions.
  • Compliance: Ensure that all testing procedures comply with relevant industry standards and regulatory requirements.
  • Maintenance: Maintain and calibrate testing equipment to ensure accurate and reliable test results.
  • Collaboration: Work closely with engineers and other technical staff to troubleshoot and resolve EMC/EMI issues.
Qualifications
  • Education: Associate degree or technical certification in electronics, electrical engineering, or a related field.
  • Experience: Previous experience in EMC/EMI testing or a related field is preferred.
  • Skills:
    • Strong understanding of electromagnetic principles and testing methodologies.
    • Proficiency in using EMC testing equipment and software.
    • Excellent analytical and problem-solving skills.
    • Attention to detail and ability to follow precise testing procedures.
    • Good communication skills for reporting and collaboration.

Work Environment:

  • This role typically involves working in a laboratory or testing facility.
  • Will require occasional travel to client sites or other testing locations.

Additional Information

Compensation:

  • Salary: $70,000-$100,000

Schedule:

  • Monday-Friday 8:30am-5:00pm

What we offer:

  • 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

Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.