Veristat is a science-driven full-service CRO and consultancy that accelerates the development of innovative therapies through strategic planning, regulatory expertise, and efficient clinical trial execution.
Southborough, Massachusetts
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 talentacquisition@veristat.com. Be vigilant.
Remote · Massachusetts, United States
The Principal Medical Writer serves as a project leader and primary author for complex regulatory documentation, specifically focusing on CMC submissions. They are responsible for mentoring team members and ensuring high-quality, compliant document finalization across various client engagements.
Remote · Colorado, United States
The Senior Medical Writer plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing and presenting scientific and statistical information in compliance with ICH and regulatory guidelines.
Remote · Massachusetts, United States
The Biostatistician II performs analysis of clinical trial data and provides statistical input for reporting results. They work largely independently with minimal oversight to support the delivery of clinical research projects.
Remote · Massachusetts, United States
The Principal Medical Writer serves as a project leader and primary author for complex regulatory documents across various service lines. They are responsible for mentoring team members and ensuring high-quality documentation that meets global health authority requirements.
Remote · North Carolina, United States
The Director of Regulatory Affairs provides strategic and operational consulting for clients, managing interactions with health authorities and the FDA. They are responsible for preparing regulatory documentation such as INDs, NDAs, and BLAs while leading cross-functional teams.
Remote · Massachusetts, United States
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for organizing, analyzing, and presenting scientific and statistical information in compliance with ICH and regulatory guidelines.
Remote · Massachusetts, United States
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing, interpreting, and presenting scientific and statistical information in compliance with ICH and regulatory standards.
Remote · Massachusetts, United States
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing and presenting scientific information in accordance with industry guidelines and company standards.
On-site
Job Description: The Senior Medical Writer - Safety Focus is a major contributor to document authorship for a variety of aggregate safety reports within the safety service line. The Medical Writer - Safety Focus will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. 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 Verista…
