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Clinical trial and observational study data management and biostatisticsPosted 29 days ago

Quality Assurance Specialist I

Full-time
On-site
Entry level
Competitive
Posted 29 days ago

Frontier Science & Technology Research Foundation, Inc. is hiring a Quality Assurance Specialist I to support the development and maintenance of its Quality Management System and electronic QMS. The role includes system administration, audits, incident and CAPA management, validation, documentation, and staff training in a clinical research environment.

Posted
29 days ago
Source
workforcenow.adp.com
Sector
Production/Manufacturing

Opens the employer's application page in a new tab

Responsibilities

  • Assist in cross office compliance efforts
  • Work with office leaders to define compliance needs
  • Conduct assessments (IAPs) and/or Gap Assessments
  • Build, enforce and improve QMS infrastructure where required
  • Regular meetings with QA personnel in Amherst and other offices
  • Ensure success of current quality initiatives by working with a cross office team of QA experts
  • Assist with incident management, CAPA management, and implementation of electronic quality management system (eQMS)
  • Performs system administrator duties in the eQMS
  • Conduct internal audits and recommend procedure improvements as needed
  • Conduct investigations into incidents of noncompliance
  • Track, monitor, and gather metrics from corrective and preventative action activities
  • Provide support to other QA team members and Project Leads
  • Assist with the eQMS quality software validation efforts, including preparing the required documentation and testing efforts
  • Maintain knowledge and expertise in regulations, trends, and industry best practices affecting the clinical research good clinical practices (GCP) environment
  • Train other office staff on the organization’s eQMS and associated policies and procedures
  • Assist in writing policies and procedures for the Quality Department
  • Assist with technical writing activities as needed
  • Create and revise documentation related to company or department policies and procedures, internal workflows, and reference guides
  • Review, proofread, and edit business correspondence (emails, letters, newsletters, or other documents) as requested
  • Assist as necessary in business development initiatives

Qualifications

  • Bachelors' degree required
  • 0-2 years of relevant experience
  • Familiarity with general clinical trial best practices for data management and Good Clinical Practice (GCP) guidelines
  • Experience in systems administration
  • Familiarity with Federal regulations affecting clinical trial data management work such as relevant FDA regulations and 21 CFR Part 11
  • Ability to work independently while managing a large number of competing deadlines
  • Ability to read and comprehend industry literature, especially for quality assurance and general compliance topics, and to conduct research to facilitate answers to compliance inquiries
  • Strong writing skills and the ability to produce documentation using proper English and grammar and in a manner to be understood by general staff and management
  • Excellent communication and interpersonal skills, along with the ability to facilitate discussion and gather information for the development of documentation or other quality assurance materials

Required skills

Clinical Practice (GCP)Clinical Trial Data ManagementSystems AdministrationFDA Regulations21 CFR Part 11

Nice to have

RQAP Certification preferredBrookline, Massachusetts, USAhttps://www.frontierscience.orgH1B SponsorshipData Powered by91Engineering and DevelopmentCustomer Service and SupportTrends of Total Sponsorships*2026(3)202520242023

Full job description

Frontier Science & Technology Research Foundation, Inc. is hiring a Quality Assurance Specialist I to support the development and maintenance of its Quality Management System and electronic QMS. The role includes system administration, audits, incident and CAPA management, validation, documentation, and staff training in a clinical research environment.

Responsibilities

  • Assist in cross office compliance efforts
  • Work with office leaders to define compliance needs
  • Conduct assessments (IAPs) and/or Gap Assessments
  • Build, enforce and improve QMS infrastructure where required
  • Regular meetings with QA personnel in Amherst and other offices
  • Ensure success of current quality initiatives by working with a cross office team of QA experts
  • Assist with incident management, CAPA management, and implementation of electronic quality management system (eQMS)
  • Performs system administrator duties in the eQMS
  • Conduct internal audits and recommend procedure improvements as needed
  • Conduct investigations into incidents of noncompliance
  • Track, monitor, and gather metrics from corrective and preventative action activities
  • Provide support to other QA team members and Project Leads
  • Assist with the eQMS quality software validation efforts, including preparing the required documentation and testing efforts
  • Maintain knowledge and expertise in regulations, trends, and industry best practices affecting the clinical research good clinical practices (GCP) environment
  • Train other office staff on the organization’s eQMS and associated policies and procedures
  • Assist in writing policies and procedures for the Quality Department
  • Assist with technical writing activities as needed
  • Create and revise documentation related to company or department policies and procedures, internal workflows, and reference guides
  • Review, proofread, and edit business correspondence (emails, letters, newsletters, or other documents) as requested
  • Assist as necessary in business development initiatives

Preferred

  • RQAP Certification preferred
  • RQAP Certification

Company

  • Clinical trial and observational study data management and biostatistics
  • Brookline, Massachusetts, USA
  • https://www.frontierscience.org/
  • Founded in 1975
  • 51-200 employees

Qualifications

  • Bachelors' degree required
  • 0-2 years of relevant experience
  • Familiarity with general clinical trial best practices for data management and Good Clinical Practice (GCP) guidelines
  • Experience in systems administration
  • Familiarity with Federal regulations affecting clinical trial data management work such as relevant FDA regulations and 21 CFR Part 11
  • Ability to work independently while managing a large number of competing deadlines
  • Ability to read and comprehend industry literature, especially for quality assurance and general compliance topics, and to conduct research to facilitate answers to compliance inquiries
  • Strong writing skills and the ability to produce documentation using proper English and grammar and in a manner to be understood by general staff and management
  • Excellent communication and interpersonal skills, along with the ability to facilitate discussion and gather information for the development of documentation or other quality assurance materials
  • RQAP Certification preferred

Required skills

  • Clinical Practice (GCP), Clinical Trial Data Management, Systems Administration, FDA Regulations, 21 CFR Part 11, Regulatory Quality Assurance Professional (RQAP) Certification

Preferred skills

  • RQAP Certification preferred, Brookline, Massachusetts, USA, https://www.frontierscience.org, H1B Sponsorship, Data Powered by, Distribution of Different Job Fields Receiving Sponsorship, 91, Represents job field similar to this job, Engineering and Development, Customer Service and Support, Trends of Total Sponsorships, *2026, (3), 2025, 2024, 2023, (2), 2022, (5), 2021, (4), 2020, Growth Stage, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 15, 2026

Work mode

On-site

Job source

workforcenow.adp.com

Company

Clinical trial and observational study data management and biostatistics

Production/Manufacturing

Clinical trial and observational study data management and biostatistics

See all 4 jobs from Clinical trial and observational study data management and biostatistics →
  • Brookline, Massachusetts, USA
  • Production/Manufacturing
  • 51-200 employees
  • Founded 1975
  • frontierscience.org

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Quality Assurance Specialist I

Clinical trial and observational study data management and biostatistics · Competitive

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