Veristat
Biotechnology • Pharmaceuticals • Science
Veristat is a specialty Contract Research Organization (CRO) that offers comprehensive clinical trial and consulting services. Particularly focused on the pharmaceutical and biotechnology sectors, Veristat supports their clients' development and regulatory strategy for complex and novel therapies. The company's expertise spans biologics, gene therapies, rare diseases, and regulatory submissions. Their services include full-service clinical trial planning, clinical trial conduct, and regulatory affairs, with a strong emphasis on adaptive designs, biostatistics, and pharmacovigilance. Veristat has been pivotal in advancing therapies through strategic consulting and clinical operations, from oncology and neurology to infectious diseases.
501 - 1000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
🔬 Science
đź’° Private Equity Round on 2021-04
Principal Medical Writer
August 21
Veristat
Biotechnology • Pharmaceuticals • Science
Veristat is a specialty Contract Research Organization (CRO) that offers comprehensive clinical trial and consulting services. Particularly focused on the pharmaceutical and biotechnology sectors, Veristat supports their clients' development and regulatory strategy for complex and novel therapies. The company's expertise spans biologics, gene therapies, rare diseases, and regulatory submissions. Their services include full-service clinical trial planning, clinical trial conduct, and regulatory affairs, with a strong emphasis on adaptive designs, biostatistics, and pharmacovigilance. Veristat has been pivotal in advancing therapies through strategic consulting and clinical operations, from oncology and neurology to infectious diseases.
501 - 1000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
🔬 Science
đź’° Private Equity Round on 2021-04
đź“‹ Description
• Independently plans and prepares regulatory documents and medical communications to support all phases of product development. • Organizes, analyzes, interprets, and presents scientific and statistical information in accordance with ICH and other regulatory guidelines, and individual company document standards. • Works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.
🎯 Requirements
• Bachelor's degree required; science-related field preferred. • Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis. • Advanced knowledge of ICH and related regulatory guidelines. • Excellent written English and keen attention to detail. • Strong interpersonal and communication skills. • Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.
🏖️ Benefits
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
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