
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.
đĄ We watch Veristat's careers page
Every 2 hours
how often we check
6
roles posted in the last 30 days
About 29 days
usual time to fill a role
32
roles closed in the last year
Selected: đšđŠ Canada â Remote.
Selected: đ Date Added.
đ 6 days ago
Senior Regulatory Affairs Project Manager leading drug-development projects at Veristat, a global clinical research organization. Coordinating regulatory, clinical, quality, CMC, and business consulting teams.
đ United States, Canada â Remote
đ” $128k - $144k / year
đ° Private equity on 2021-05
â° Full Time
đ Senior
đ·ââïž Project Manager
đŠ H1B Visa Sponsor
đ» Ghost score 0%
đ October 5
Biostatistician analyzing clinical trial data and reporting results for Veristat, a global clinical research organization accelerating life-changing therapies.
đšđŠ Canada â Remote
đ” $92k - $107k / year
đ° Private equity on 2021-05
â° Full Time
đĄ Mid-level
đ Senior
đ§Ș Clinical Research
đ» Ghost score 0%
đ September 29
Principal Medical Writer leading clinical regulatory documentation for Veristatâs life-science clients. Authoring submissions, leading project teams, and mentoring medical writers.
đ United States, Canada â Remote
đ Massachusetts â Remote
đ” $132k - $151k / year
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 0%
đ September 23
Principal Medical Writer preparing regulatory documents and medical communications for Veristatâs life-sciences therapy development programs. Interpreting scientific and statistical information under ICH guidelines.
đ United States, France, +4 more countries â Remote
đ Massachusetts â Remote
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 12%
đ September 23
Senior Medical Writer preparing regulatory documents and medical communications for Veristatâs life-sciences therapy development programs. Supporting global clinical and regulatory submissions under ICH guidelines.
đ United States, France, +5 more countries â Remote
â°ïž Colorado â Remote
đ° Private equity on 2021-05
â° Full Time
đ Senior
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 12%
đ August 27
Director of Regulatory Affairs advising pharmaceutical and biotech clients on FDA development strategies. Preparing IND/NDA/BLA documentation and leading Health Authority interactions.
đ United States, Canada â Remote
đČ North Carolina â Remote
đ” $195k - $223k / year
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ Compliance
đŠ H1B Visa Sponsor
đ» Ghost score 12%
đ August 17
Principal Medical Writer preparing nonclinical regulatory submissions and medical communications for Veristatâs drug-development services. Leading CTD sections, synthesizing scientific data, and guiding cross-functional teams through health-authority submission processes.
đ United States, Canada â Remote
đ Massachusetts â Remote
đ” $132k - $151k / year
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 16%
đ August 13
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.
đ United States, Canada â Remote
đ Massachusetts â Remote
đ” $142k - $153k / year
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 18%
đ August 7
Senior Medical Writer leading clinical regulatory documents for Veristat, a life-sciences services company. Managing client projects and supporting submissions that accelerate therapies to patients.
đ United States, Canada â Remote
đ Massachusetts â Remote
đ” $116k - $128k / year
đ° Private equity on 2021-05
â° Full Time
đ Senior
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 20%
đ July 15
Principal Medical Writer developing regulatory documents and medical communications. Collaborating with internal and external teams to support product development phases.
đ United States, Canada â Remote
đ Massachusetts â Remote
đ” $132k - $151k / year
đ° Private equity on 2021-05
â° Full Time
đŽ Lead
đ„đ Medical Writer
đŠ H1B Visa Sponsor
đ» Ghost score 30%