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Specialist, Quality Assurance

Role overview

Qualifications

  • Bachelor's degree
  • 2 years of experience in Quality Assurance
  • 4 years of experience in Clinical Research
  • Portuguese and English language speaker required, Spanish is a plus

Responsibilities

  • Ensure the highest standards of patient safety and data integrity at clinical research sites
  • Conduct comprehensive reviews of study-specific regulatory binders and clinical documents
  • Execute the yearly corporate audit plan and track quality assurance audits
  • Partner with research staff to resolve compliance issues and monitor CAPA plans

Key facts

Other skills

  • Quality Assurance
  • Technical Acumen
  • Communication
  • Teamwork
  • Detail Oriented
  • Decision Making
  • Organizational Skills
  • Curiosity
  • Self-Motivation

About the company

Care Access logo

Care Access

Research

Care Access is a global research site that accelerates the availability of new treatments by enabling more communities to gain access clinical research.

Company details

Company typeSME
IndustryResearch
Company size501 - 1000

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Job description

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com.

How This Role Makes a Difference

Care Access is seeking a dedicated, experienced, and innovation-driven Quality Assurance Specialist (GxP) to support the success of the Quality Assurance Department and organizational compliance activities. The Quality Assurance Specialist will be responsible for closely monitoring the quality and compliance of clinical work at both traditional trial sites and decentralized trials.QA specialist will directly support of quality initiatives, audit functions, CAPA systems and promote inspections readiness.  Working in support of the Associate Director of Quality Assurance, the Quality Assurance Specialist will ensure that Care Access maintains a high level of quality while executing clinical trials according to Care Access SOPs, GCP, and FDA/ICH Guidelines 

How You'll Make An Impact

  • Site-Level Quality & Data Integrity: Ensure the highest standards of patient safety and data integrity at clinical research sites through regular quality assurance reviews, site quality support, and assurance compliance with Standard Operating Procedures. 
  • GCP Regulatory Document Review: Conduct comprehensive reviews of study-specific regulatory binders and clinical documents to verify they are accurately completed and maintained per GCP standards. 
  • Audit Execution & Tracking: Execute the yearly corporate audit plan, systematically tracking quality assurance audits, monitoring related activities, and preparing detailed outcome reports for management. 
  • Issue Resolution & CAPA Management: Partner directly with research staff and Principal Investigators (PIs) to resolve identified compliance issues, developing, tracking, and monitoring Corrective and Preventative Action (CAPA) plans. 
  • External Audit & Inspection Support: Coordinate and provide hands-on operational support for on-site audits and inspections conducted by external providers, sponsors, and regulatory agencies. 
  • Quality Systems Administration: Provide ongoing administrative support to the Quality Department by maintaining internal quality systems, compliance trackers, and operational programs. 
  • SOP Development & Maintenance: Participate in the routine review, drafting, and maintenance of quality assurance Standard Operating Procedures (SOPs) to ensure alignment with evolving regulations. 
  • Cross-Functional Compliance Advisory: Act as an internal quality resource to provide ongoing guidance and best-practice recommendations to site personnel and clinical project teams. 
  • Regulatory compliance: be knowledgeable of evolving GxP guidelines. Ability to critically think, eagerness to learn, and commitment to ensuring compliance. Knowledge of and able to interpret regulatory guidance’s such as 21 CFR Part 11/ Part 312, ICH GCP E6 (R3).  
  • Inspection readiness: promote a culture of inspections readiness and continuous improvement. Be flexible to work with risk-based audit agendas and shifting priorities.
  • Create and deliver training on Quality and Improvement activities  
  • Support completion of RFP/RFI (Request for proposals/information) 
  • Willingness to learn and engage with digital technologies  
  • Provide AI project quality support and consultation 
  • Support other activities related to the management of QMS and accuracy of data 
  • Support GxP and non GxP quality issues and/or projects needing quality consultation and support    

The Expertise Required 

  • Ability to work independently, remain objective, and manage multiple assignments.  
  • Remain flexible and work in evolving regulatory environments. 
  • Display an openness to innovative and compliant approaches to conducting research and health services activities 
  • Technical proficiency is required to work daily in QMS and utilize various software and platforms across the business. 
  • Ability to drive change and demonstrate impact across the business.  
  • Excellent writing and presentation skills and ability to lead and coach staff and cross-functional teams.  
  • Excellent working knowledge of medical and research terminology 
  • Excellent working knowledge of federal regulations and Good Clinical Practices (GCP) 
  • Attention to detail 
  • Ability to communicate and work effectively with a diverse team of professionals 
  • Strong Organizational Skills 
  • Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors 
  • Work effectively and collaboratively with other team members to accomplish mutual goals. Bring a positive and supportive attitude to achieving these goals 
  • Demonstrate decision making skills 
  • Curiosity and passion to learn, innovate, able to communicate any possible risks and get things done 
  • Friendly, outgoing personality with the ability to maintain a positive attitude under pressure 
  • High level of self-motivation and energy 
  • Ability to work independently in a fast-paced environment with minimal supervision 
  • Must have a client service mentality 
  • Experience with supporting multiple sites and identifying gaps 
  • Experience with internal and external audits: FDA, GCP, SOPs 
  • Experience with supporting multiple sites and identifying improvement gaps 

Certifications/Licenses, Education, and Experience

  • Minimum Education:
    • Bachelor’s degree  
  • Minimum Experience:
    • 2 years of experience in Quality Assurance 
    • 4 years of experience in Clinical Research working in a compliance or GCP relevant role  
    • Portuguese and English language speaker required, Spanish is a plus. 

How We Work Together

  • Location: Remote within the country
  • Travel: Minimal (<10%), planned in advance.

Benefits & Perks

  • Paid Time Off (PTO) and Company Paid Holidays
  • Medical, dental, and vision insurance plan options

#LI-Remote

Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. 

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com

Mandatory Employer Disclosures:
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. 

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Marcus Rivera

Chief Revenue Officer

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