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…
Profil d’entreprise sauvegardé
Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.
Description complète de l’entreprise
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.
-
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.
Abonnés LinkedIn
32 931
Personnes associées sur LinkedIn
494
Bureaux déclarés
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
Catégories d’activité
Life Science
Medical
Pharmaceutical
Autres noms enregistrés
Veristat
Spécialités
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
Le profil indique une agence de recrutement
Non
Investissement total déclaré
0
La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.
7+ ansCandidates 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+ ansCandidates 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+ ans3+ gestionCandidates 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.