
501 - 1000 employees
đŒ Consulting
đ„ Healthcare
đ Pharmaceuticals
đ° Private equity on 2021-05
Consulting âą Healthcare âą Pharmaceuticals
Veristat is a clinical development services company that provides end-to-end, regulatory-focused support for biopharmaceutical and medical device sponsors. The firm offers full-service clinical trial planning and conduct, regulatory affairs and submission support (including NDA/MAA and interactions with agencies like PMDA), statistical and biometrics services, medical writing, pharmacovigilance, and project management for complex therapeutic areas such as oncology, rare diseases, neurology, biologics, and cell & gene therapies. Veristat operates as a B2B partner to biotech and pharmaceutical organizations to reduce development risk and accelerate regulatory approval.
đ„ 13 hours ago
đ United States, France, +4 more countries â Remote
đ Massachusetts â Remote
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŠ H1B Visa Sponsor
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501 - 1000 employees
đŒ Consulting
đ„ Healthcare
đ Pharmaceuticals
đ° Private equity on 2021-05
Consulting âą Healthcare âą Pharmaceuticals
Veristat is a clinical development services company that provides end-to-end, regulatory-focused support for biopharmaceutical and medical device sponsors. The firm offers full-service clinical trial planning and conduct, regulatory affairs and submission support (including NDA/MAA and interactions with agencies like PMDA), statistical and biometrics services, medical writing, pharmacovigilance, and project management for complex therapeutic areas such as oncology, rare diseases, neurology, biologics, and cell & gene therapies. Veristat operates as a B2B partner to biotech and pharmaceutical organizations to reduce development risk and accelerate regulatory approval.
âą Independently plan and prepare a range of regulatory documents and medical communications supporting all phases of product development. âą Organize, analyze, interpret, and present scientific and statistical information in accordance with ICH and other regulatory guidelines and company document standards. âą Work under the direction of Medical Writing management. âą Collaborate with cross-functional internal and external document production teams.
âą Bachelorâs degree required; science-related field preferred. âą 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. âą Advanced knowledge of ICH and related regulatory guidelines. âą Excellent written English and keen attention to detail. âą Strong interpersonal and communication skills. âą Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.
âą Remote working âą Flexible time off âą Paid holidays âą Medical insurance âą Tuition reimbursement âą Retirement plans
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