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…
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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.
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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.
LinkedIn followers
32,931
People associated on LinkedIn
494
Reported office locations
134 Turnpike Rd, Ste 200, Southborough, Massachusetts 01772, US
2801 Slater Road, Ste 100, Morrisville, North Carolina 27560, US
TAIPEI, Hsin Ji 9F-1., No.460, Sec. 4 Xinyi Rd., Xinyi Dist., Taipei City, 11052, TW
36 rue de l'intendance, Lotissement de l'intendance, Fréjus, 83600, FR
Carrer de Sant Antoni, Maria Claret 167, Barcelona, 08025, ES
Aeschenvorstadt 52, Basel, CH-4051, CH
Business categories
Life Science
Medical
Pharmaceutical
Other recorded names
Veristat
Specialties
Strategic Consulting
Safety Management
Data Management
Biostatistics
Statistical Programming
Project Management
Medical Writing
Regulatory Submissions
Adaptive Clinical Trial Design
Site Monitoring
Regulatory Consulting
Clinical Trial Patient Recruitment
Clinical Trial Data Standardization
Clinicl Trial Design
Clinical Trial Management
US Regulatory Agent
Pharmacovigilance
Marketing Applications Support
IND Support
Regulatory Publishing
Biologic
Gene Therapy
Full-service CRO
and Oncology Clinical Trials
Profile identifies a recruitment agency
No
Reported total investment
0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
7+ YOECandidates need at least 7 years of medical writing experience in a CRO or pharmaceutical/biotech setting, plus advanced knowledge of ICH guidelines. Excellent written English, strong attention to detail, and advanced Microsoft Word skills are required; a science degree is preferred.
3+ YOECandidates need a bachelor's degree, ideally in a science field, and at least 3 years of formal medical writing experience, with 5 years preferred. They must know ICH guidelines well, write excellent English, and be advanced in Microsoft Word.
6+ YOE3+ MgmtCandidates need a bachelor's degree in life or health sciences, 6 to 8 years of regulatory experience at a CRO or pharmaceutical company, and 3 years of project management. They also need strong communication, planning and team-building skills and knowledge of ICH guidelines.
3+ YOECandidates need at least three years in cybersecurity, IT operations or a related technical role, plus experience reviewing alerts, logs and reports. Strong writing, judgment and independent remote work are needed, along with availability during Eastern Time business hours.
Cybersecurity, Reporting, Process improvement, Documentation, Presentation skills, Work independently