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Protocol Associate Jobs in Massachusetts (NOW HIRING)

Distribution Associate

Marlborough, MA ยท On-site

$23 - $26/hr

Distribution Associate Location: EES Marlborough Department: commercial warehouse distribution ... Follow all safety protocols and guidelines to ensure a safe working environment. * Assist with the ...

Research Associate I

Worcester, MA ยท On-site

$43K/yr

Research Associate I Minimum Salary US-MA-Worcester Job Location 1 month ago(7/7/2026 10:32 AM ... Maintain accurate records, may modify protocols with the approval of the PI or designee * Review ...

Research Associate II Minimum Salary US-MA-Worcester Job Location 3 days ago(8/7/2026 1:58 PM ... Maintain accurate records, may modify protocols with the approval of the PI or designee * Review ...

Research Associate I

Worcester, MA ยท On-site

$43K/yr

Research Associate I Minimum Salary US-MA-Worcester Job Location 3 days ago(8/7/2026 1:51 PM ... Maintain accurate records, may modify protocols with the approval of the PI or designee * Review ...

IPM Associate

Littleton, MA ยท On-site

$18/hr

Job Summary: The IPM Associate will play a critical role in maintaining plant health through ... Participate in lift training and follow all safety protocols. * Maintain a positive attitude and ...

IPM Associate

Littleton, MA ยท On-site

$18/hr

Job Summary: The IPM Associate will play a critical role in maintaining plant health through ... Participate in lift training and follow all safety protocols.Maintain a positive attitude and ...

Research Associate II Minimum Salary US-MA-Worcester Job Location 3 weeks ago(7/20/2026 8:29 AM ... Maintain accurate records, may modify protocols with the approval of the PI or designee * Review ...

Showing results 21-40

Protocol Associate information

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

AspectProtocol AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, often in life sciences or related fieldBachelor's degree, often in health sciences or related field
Work EnvironmentResearch institutions, pharmaceutical companies, clinical trial sitesHospitals, clinics, research centers
Employer & Industry UsageUsed in clinical research and pharmaceutical industriesCommon in clinical trial management and healthcare settings
Common Search & Comparison IntentYesYes

The main difference between a Protocol Associate and a Clinical Research Coordinator lies in their specific roles within clinical trials. Protocol Associates primarily focus on managing trial documentation, ensuring protocol compliance, and supporting regulatory submissions. Clinical Research Coordinators are more involved in patient recruitment, data collection, and day-to-day trial operations. Both roles require similar educational backgrounds and work in related environments, but their responsibilities differ based on the trial phase and organizational structure.

What does a protocol associate do?

Protocol Associates play a vital role in ensuring that high-profile events and meetings run smoothly by managing logistics, adhering to diplomatic protocols, and coordinating with various stakeholders. They often handle guest lists, seating arrangements, and the flow of official communications, ensuring all cultural and organizational standards are met. Collaboration with event planners, security teams, and senior officials is common, making strong organizational and interpersonal skills essential. This role provides exposure to international relations and offers significant opportunities for growth in diplomatic or governmental settings.

What are the key skills and qualifications needed to thrive as a protocol associate?

To thrive as a Protocol Associate, you need strong organizational abilities, attention to detail, and a background in international relations or event management, often supported by a relevant bachelor's degree. Familiarity with scheduling software, database management systems, and sometimes knowledge of diplomatic protocols or languages is valuable. Excellent interpersonal skills, cultural sensitivity, and clear communication help build relationships and manage high-profile events smoothly. These competencies ensure that all protocol activities are executed flawlessly, maintaining professionalism and fostering positive diplomatic or organizational relations.

What is a protocol associate?

Protocol Associates are professionals who assist in planning, organizing, and executing formal events, meetings, or ceremonies, often for government, diplomatic, or corporate organizations. They ensure that events adhere to proper procedures, etiquette, and established protocols. Their responsibilities may include managing guest lists, coordinating logistics, and advising on cultural customs to facilitate smooth interactions between parties. Protocol Associates play a key role in maintaining the organization's image and fostering positive relationships with stakeholders.
What are the most commonly searched types of Protocol jobs in Massachusetts? The most popular types of Protocol jobs in Massachusetts are:
What cities in Massachusetts are hiring for Protocol Associate jobs? Cities in Massachusetts with the most Protocol Associate job openings:

Research Associate - Open Rank

UMass Med School

Worcester, MA โ€ข On-site

$73K/yr

Other

Re-posted 5 days ago


Job description

Research Associate - Open Rank
Minimum Salary US-MA-Worcester
Job Location 3 days ago(8/7/2026 1:52 PM)
Requisition Number 2026-49471 # of Openings 1 Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit Professional Position Type Full-Time Min USD $40,000.00/Yr. Max USD $73,000.00/Yr.
Overview

POSITION SUMMARY:

Under the direction of the Principal Investigator (PI) or designee, the Research Associate provides operational support to the laboratory. The Research Associate will perform research experiments as defined by the PI.

This is an open-rank posting (there are 4 levels of Research Associate) - candidates will be hired into the level commensurate with their experience.

The Ling lab was established at GCM in 2024, focusing on developing innovative gene therapies for neurological and mitochondrial diseases. Our active research projects include:

    Gene editing in mitochondrial DNA: we use base editing technologies to create mouse models for gene mutations in the mitochondrial DNA, and develop gene therapies targeting the most frequent pathogenic variants.
  • Gene therapy for vestibular schwannoma: we engineer novel gene therapies to slow vestibular schwannoma growth and prevent hearing loss. We leverage multi-omics patient data and develop patient-derived 3D tumoroid models to accelerate the development of an effective and safe gene therapy for the patients.
Responsibilities

ESSENTIAL FUNCTIONS:

Research Associate I:

  • Perform laboratory experiments and may be responsible for a single research project.
  • Utilize all software relevant to experiment and equipment used.
  • Interpret data, form conclusions and decide on next steps under the direction of the PI or designee.
  • Maintain accurate records, may modify protocols with the approval of the PI or designee.
  • Review literature, publications and grants relevant to assigned projects.
  • Record results according to established lab, sponsor & university protocol
  • Assist with performing data analysis and/or mathematical computations.
  • Maintain a detailed lab notebook according to lab practice.
  • Present findings at lab/group meetings
  • Monitor laboratory supply levels and order as noted.
  • Prepare and label buffers, media, solutions, etc.
  • Assist with and comply with all safety regulation and infection control standards.
  • Train on IACUC, IRB, EHS, Radiation safety protocols
  • Comply with all applicable state, federal university, and sponsor policies and agreements.
  • Provide support with identifying problems and challenges, propose resolutions, implement appropriate solutions.
  • Provide support with drafting standard operation procedures in compliance to EHS regulation specific for the lab.
  • Perform other duties as required.

Research Associate II:

Duties noted above plus:

  • May assist with the training of new lab personnel.
  • Provide support with drafting standard operation procedures in compliance to EHS regulation specific for the lab.
  • May assist with drafting manuscript sessions.

Research Associate III:

Duties noted above plus:

  • Perform complex laboratory experiments and may be responsible for one or more independent research projects.
  • Perform in-depth data analysis and/or mathematical computations.
  • Compile and analyze data and present it in a format suitable for publication according to PI specifications.
  • May oversee laboratory supply levels and order as needed; negotiate with suppliers to optimize available resources.
  • Monitor laboratory equipment service contracts and monitor maintenance on laboratory equipment.
  • May manage general operations of the laboratory, including lab personnel, procedures, and projects.
  • May create new protocols and/or modify defined protocols, as necessary, and with the approval of the PI.
  • Prioritize and perform several tasks or procedures simultaneously with attention to detail.
  • Perform duties and experiments with independence.
  • Provide training of new lab personnel.
  • May monitor laboratory spending in accordance with budget guidelines provided by PI or designee.
  • May assist with budget and/or operational aspects of grant and contract funding.

Research Associate IV:

Duties noted above plus:

  • This position will contribute significantly to the management of the research program and will be involved in multiple aspects of the research projects and lab maintenance activities.
  • Independently design and perform multiple complex laboratory experiments.
  • Interpret data, form conclusions, and decide on next steps with a high degree of independence.
  • Maintain laboratory supply levels and order as noted.
  • Manage laboratory equipment service contracts and coordinate maintenance on laboratory equipment.
  • Monitor and enforce all safety regulations and infection control standards.
  • Identify and write standard operation procedures in compliance to EHS regulation specific for the lab
  • Train on IACUC, EHS, Radiation safety protocols
  • Manage daily operations of the laboratory, including lab personnel, procedures, and projects.
  • Identify problems and challenges, propose resolutions, implement appropriate solutions.
  • Develop and implement new protocols and/or modify defined protocols, as necessary, and with the approval of the PI
  • Mentor and train lab personnel on proper lab conduct and techniques.
  • Manage laboratory spending in accordance with budget guidelines provided by PI or designee.
  • Assist with budget and/or operational aspects of grant and contract proposals.
  • Negotiate with vendors to optimize available resources.
  • Contribute independently to writing sections for manuscripts and grants.
  • Direct the activities of research support staff.
  • Perform other duties as required.
Qualifications

REQUIRED QUALIFICATIONS:

Research Associate I

  • Bachelor's degree in Biological or Natural Science, or equivalent experience
  • Basic understanding of lab safety and protocols
  • Knowledge of Microsoft Office products
  • Ability to analyze data in a quantitative and objective manner.
  • Ability to work in a team environment.

Research Associate II

  • Requirements noted for RA I plus:
  • 18 months of relevant research experience with a Bachelor's Degree in Biological or Natural Science or 0 years with a related Master's Degree.

Research Associate III

  • Requirements noted for RA I plus:
  • 3+ years of relevant research experience with a Bachelor's Degree in Biological or Natural Science or 1 year relevant research experience with a related Master's Degree

Research Associate IV

  • Requirements noted for RA I plus:
  • 5+ years of relevant research experience with a Bachelor's Degree in Biological or Natural Science or 3+ years relevant research experience with a related Master's degree.