Principal Medical Writer leading CMC regulatory submissions for Veristat’s life - sciences clients. Authoring Modules 3 and 2.3 while guiding project teams and mentoring regulatory writers.
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Veristat
Currently Hiring
About the company
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.
AtVeristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties.
Ourscientific 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, ourversatile approach and bold scientific thinking make the impossible possible.
Dependon our game-changing expertise and reliable execution for fast results and positiveimpact 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.
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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.
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11 jobs found
Principal Medical Writer leading clinical regulatory documentation for Veristat’s life - science clients. Authoring submissions, leading project teams, and mentoring medical writers.
IT Security Analyst II coordinating cybersecurity monitoring, MSP oversight, audits, and incident follow - up. Supporting Veristat’s global life - sciences services and regulated technology environments.
Senior Medical Writer preparing regulatory documents and medical communications for Veristat’s life - sciences therapy development programs. Supporting global clinical and regulatory submissions under ICH guidelines.
Principal Medical Writer preparing regulatory documents and medical communications for Veristat’s life - sciences therapy development programs. Interpreting scientific and statistical information under ICH guidelines.
Vendor Manager overseeing Veristat’s global vendor lifecycle and strategic procurement. Supporting clinical trials through sourcing, contracting, KPI governance, and vendor performance management.
Pharmacovigilance associate managing serious adverse events and patient safety for Veristat’s clinical research programs. Supporting safety reporting, training, databases, sponsors, and investigator sites.
Principal Clinical Data Manager leading clinical research data management, quality, and database lock activities at Veristat. Managing complex studies and mentoring clinical data management teams.
Director of Regulatory Affairs advising pharmaceutical and biotech clients on FDA development strategies. Preparing IND/NDA/BLA documentation and leading Health Authority interactions.
Senior Medical Writer leading clinical regulatory and clinical document authorship for Veristat, a life - sciences consultancy accelerating therapies. Managing projects, teams, clients, and submission deliverables.
Principal Medical Writer preparing regulatory documents and medical communications for Veristat, a clinical research organization accelerating life - changing therapies. Supporting product development through scientific analysis, ICH compliance, and cross - functional document collaboration.