Job Description:
Senior Quality Control Associate
Under the direction of Medical Writing management, the Senior Quality Control Associate provides a thorough quality control (QC) review of regulatory documents and medical communications to support all phases of product development. These documents include, but are not limited to, clinical study reports, study protocols, subject safety narratives, informed consent documents, investigator’s brochures, clinical and nonclinical sections of regulatory submissions, and manuscripts.
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
- Learn more about our core values here!
What we look for
- Bachelor’s degree required; science-related field preferred.
- Minimum of 3 years of experience working in a life science or clinical research environment, preferably in a contract research organization (CRO) or pharmaceutical/biotechnology setting. Medical/technical writing experience and/or experience in a QC function is essential.
- Excellent command of the English language (grammar, spelling, English usage, punctuation), ability to focus and maintain a high level of attention to detail, strong interpersonal and communication skills, and ability to function collaboratively in a team environment are mandatory.
- Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.
- Familiarity with medical terminology and statistical concepts preferred.
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
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Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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What We Do
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat. - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at [email protected]. Be vigilant
