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 · Ontario, Canada
The Senior Project Manager leads the planning and execution of complex clinical trial and regulatory projects. They serve as the primary interface between internal departments, company leadership, sponsors, and external vendors.
Remote · British Columbia, Canada
The Senior Project Manager leads the planning and execution of complex clinical trial and regulatory projects. They serve as the primary interface between internal departments, company leadership, sponsors, and external vendors.
Remote · Quebec, Quebec, Canada
The Senior Project Manager leads the planning and execution of complex clinical trial and regulatory projects. They serve as the primary interface between internal departments, company leadership, sponsors, and external vendors.
Remote · Quebec, Quebec, Canada
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support all phases of product development. They are responsible for organizing, analyzing, and presenting scientific and statistical information in accordance with ICH and company standards.
Remote · Ontario, Canada
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support all phases of product development. They are responsible for organizing, analyzing, and presenting scientific and statistical information in accordance with ICH and company standards.
Remote · British Columbia, Canada
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support all phases of product development. They are responsible for organizing, analyzing, and presenting scientific and statistical information in accordance with ICH and company standards.
Remote · Massachusetts, United States
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. This involves analyzing and presenting scientific and statistical information according to ICH and company 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.
Remote · Massachusetts, United States
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support all phases of product development. They lead project teams, author high-quality submission-level documents, and collaborate with cross-functional teams to ensure regulatory compliance.
Remote · Massachusetts, United States
The Senior Medical Writer leads the authorship of clinical regulatory documents and manages smaller projects while supporting larger engagements. They interface directly with clients to ensure goals are met and maintain professional business relationships.
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…
