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Research Associate Jobs in Windham, NH (NOW HIRING)

RevBio, Inc.

Clinical Research Associate

Lowell, MA · On-site

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United ...

RevBio, Inc.

Clinical Research Associate

Lowell, MA · On-site

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United ...

CYNET SYSTEMS

Research Associate

Waltham, MA · On-site

$40 - $45/hr

Job Overview: Pay Range: $40.97hr - $45.97hr Requirement/Must Have: * Minimum 2-3 years of experience depending on level of education. * Bachelor's degree with 3+ years of experience or Master ...

Adecco

Research Associate I

Waltham, MA · On-site

$44.39/hr

... research teams. Work Location Waltham, Massachusetts Compensation: $44.39 per hour Pay Details: $44.39 per hour Benefit offerings available for our associates include medical, dental, vision, life ...

Polen Capital

Junior Research Associate

Waltham, MA · On-site

$75 - $125/hr

Position The High Yield Junior Research Associate will have the opportunity to gain financial skills as well as learn the intricacies of fundamental research. Working directly with experienced ...

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All JobsResearch Associate JobsResearch Associate Jobs in Windham, NH

Research Associate information

See Windham, NH salary details

$17

$33

$48

How much do research associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for research associate in Windham, NH is $33.97, according to ZipRecruiter salary data. Most workers in this role earn between $27.36 and $38.65 per hour, depending on experience, location, and employer.

What is a research associate?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

What does a research associate do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

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

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What are some typical challenges a research associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

What qualifications do you need to be a research associate?

Research associates typically need a bachelor's degree in a relevant field such as science, engineering, or social sciences. Many positions prefer or require a master's degree or higher, along with strong analytical skills, proficiency with research tools, and experience in data collection and analysis.
More about Research Associate jobs

What are the most commonly searched types of Research jobs in Windham, NH?

The most popular types of Research jobs in Windham, NH are:

What job categories do people searching Research Associate jobs in Windham, NH look for?

The top searched job categories for Research Associate jobs in Windham, NH are:

What cities near Windham, NH are hiring for Research Associate jobs?

Cities near Windham, NH with the most Research Associate job openings:

Research Associate jobs near you
Infographic showing various Research Associate job openings in Windham, NH as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $70,663 per year, or $34 per hour.

Clinical Research Associate

RevBio, Inc.

Lowell, MA • On-site

Full-time

Re-posted 14 days ago

Job description

Job Description:

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United Kingdom. This individual will work closely with investigative sites, internal team members, and external partners to help ensure that clinical trials are conducted in accordance with study protocols, applicable regulations, Good Clinical Practice, and corporate objectives.
The Clinical Research Associate will play a key role in site management and study execution, including supporting site initiation, training, routine monitoring, and close-out activities as applicable. They will assist in ensuring that sites are properly trained on study protocols, investigational use requirements, and study procedures, and will help monitor adherence to protocol, informed consent requirements, data collection expectations, and reporting obligations. The Clinical Research Associate will also support the review of study data, identification and follow-up of discrepancies or compliance issues, and timely communication of site needs, risks, and study progress to RevBio headquarters.
This role requires strong attention to detail, organization, and communication skills, as well as the ability to build productive working relationships with surgeons, clinical staff, and research coordinators. The Clinical Research Associate will help maintain effective communication between clinical sites and RevBio, support site performance and enrollment efforts, assist with essential study documentation, and contribute to inspection readiness and overall study quality.
In addition to supporting study execution, the Clinical Research Associate may assist with conference attendance, investigator engagement, clinical material preparation, and other activities that strengthen RevBio’s clinical operations and external relationships. The successful candidate will be expected to develop a detailed understanding of RevBio’s products, clinical studies, and therapeutic applications, and to serve as a reliable operational partner in the advancement of the company’s clinical programs.
Essential Duties and Responsibilities:

Clinical Operations Management
·       Interface with RevBio team members and clinical subject matter experts to develop working knowledge of the clinical applications, study requirements, and product use considerations for Tetranite in each indication under investigation. 
·       Support the day-to-day execution of clinical studies across multiple indications and geographic regions in accordance with protocol, Good Clinical Practice, applicable regulations, and company procedures. 
·       Train and support clinical sites on study protocols, investigational product use, and applicable Instructions for Use (IFU) under the direction of RevBio leadership. 
·       Collect, collate, organize, and track scientific and clinical study data from participating sites. 
·       Attend surgical enrollment visits and site interactions, as needed, to support protocol adherence, product use compliance, and strong working relationships with investigators and site staff. 
·       Monitor site-level trial progress and communicate status updates, risks, and issues to RevBio headquarters to support compliance with protocol, timelines, and regulatory requirements. 
·       Follow up with investigators and site personnel to support timely completion of EDC entries, source documentation needs, query resolution, and required data uploads. 
·       Review site activity and supporting documentation to assist with payment approvals and verification of corresponding product delivery and data submission. 
·       Assist in the preparation and submission of clinical trial protocols, informed consent documents, study materials, and regulatory documentation required to initiate and maintain clinical studies, including amendments and supplements. 
·       Assist in the preparation and submission of ethics committee and IRB applications, including supplements, renewals, and amendments as needed. 
·       Maintain organized, accurate, and complete clinical site files and documentation packages in accordance with RevBio’s Quality Management System and study requirements. 
·       Assist with site initiation, routine monitoring, site communication, and closeout activities as applicable. 
·       Escalate site issues, protocol deviations, data concerns, and operational challenges to appropriate internal team members in a timely manner. 
·       Support the investigation and follow-up of adverse events in collaboration with the clinical trial team, including the Principal Investigator, site personnel, and RevBio team members, ensuring accurate documentation and timely communication. 
·       Assist in preparing adverse event narratives, case summaries, and supporting materials for review by the Clinical Events Committee (CEC), Data Safety Monitoring Board (DSMB), and other study oversight groups, as applicable.
·       Perform other duties as assigned to support clinical study execution and operational needs. 
 
Site Relationship Management and Business Development
·       Serve as RevBio’s primary day-to-day contact for assigned clinical sites, helping maintain productive and professional working relationships. 
·       Build and maintain strong relationships with surgeons, clinical staff, research coordinators, and hospital personnel to support successful study execution. 
·       Support identification and preliminary evaluation of potential new clinical sites and Principal Investigators in coordination with RevBio headquarters. 
·       Assist with site initiation, training, and ongoing engagement activities to promote site readiness, enrollment, and compliance. 
·       Support the development and organization of training materials, training logistics, and educational resources for new investigators and study personnel. 
·       Help identify opportunities for relationship building, investigator engagement, and potential future collaboration within the clinical and research communities. 
 
External Engagement and Scientific Communication
·       Represent RevBio professionally during site visits, investigator meetings, conferences, and external interactions as assigned. 
·       Support preparation of investigators and internal team members for scientific meetings and professional conference presentations. 
·       Assist in the preparation of clinical study summaries, slide materials, posters, abstracts, and other scientific communications. 
·       Contribute to manuscripts, conference abstracts, and grant support materials as requested. 
·       Maintain current knowledge of study data, product information, and clinical developments to support effective communication with external stakeholders. 
 
Cross-Functional Collaboration
·       Interface with project leaders, internal team members, and external vendors or contractors to support coordination of study activities and site needs. 
·       Work closely with RevBio’s engineering, regulatory, quality, and clinical teams to communicate site feedback, surgeon observations, and study execution needs. 
·       Support the identification and communication of practical solutions to site-level clinical and logistical challenges. 
·       Provide timely updates on site activity, study status, and operational needs to support internal alignment and decision-making. 
·       Perform other tasks as needed to support RevBio’s clinical, scientific, and strategic objectives.
 


 

Essential Education, Skills, Environment Education and Work Experience:

  • Bachelor’s degree in Engineering, Biology, Physiology, Life Sciences, or a related field required. 
  • 0–5 years of experience in clinical research, site management, monitoring, or medical device/pharmaceutical trials. International experience preferred. 
  • Experience supporting the execution of clinical studies at the site level, including site communication, training, monitoring support, and study documentation. 
  • Demonstrated ability to work independently while managing multiple priorities and meeting deadlines. 
  • Strong organizational skills with meticulous attention to detail and accuracy. 
  • Effective oral and written communication skills, with the ability to interact professionally with surgeons, clinical staff, coordinators, and internal team members. 
  • Proficient in MS Office Suite (Word, Excel, PowerPoint), Smartsheet, Viedoc or similar EDC platforms, and project tracking tools. 
  • Experience supporting clinical trial documentation, data collection, query resolution, and site follow-up activities preferred. 
  • Exposure to manuscript support, abstract preparation, scientific presentations, and/or grant applications is preferred. 
  • Comfortable working on high-risk, early-stage technologies in a fast-paced, deadline-driven environment. 
 
Specialized Knowledge and Skills:
  • Working knowledge of clinical trial processes, Good Clinical Practice, and applicable regulatory requirements in relevant geographic regions, including the United States, Europe, and the United Kingdom. 
  • Ability to work effectively in multicultural, multidisciplinary environments. 
  • Strong interpersonal skills and ability to build productive working relationships with medical professionals, research coordinators, and site personnel. 
  • Ability to identify, communicate, and help resolve site-level operational and compliance issues. 
  • Familiarity with site interactions, conference participation, and scientific communication is preferred. 
  • Self-motivated and resourceful, with a willingness to take initiative and support a broad range of clinical activities. 
  • Entrepreneurial mindset and flexibility to adapt to changing priorities in a growing organization. 
  • High level of professionalism and discretion in representing company interests. 
  • Willingness and ability to travel extensively across the United States, Europe, and the United Kingdom, up to 50–75% as required. 
  • Commitment to doing what is needed to support a fast-growing start-up in achieving clinical and business milestones.