
501 - 1000 employees
💊 Pharmaceuticals
🧬 Biotechnology
🤝 B2B
💰 Private equity on 2021-05
Pharmaceuticals • Biotechnology • B2B
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.
🔥 2 hours ago
🇺🇸 United States – Remote
💵 $128k - $140k / year
⏰ Full Time
🟠 Senior
👷♀️ Project Manager
🦅 H1B Visa Sponsor
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501 - 1000 employees
💊 Pharmaceuticals
🧬 Biotechnology
🤝 B2B
💰 Private equity on 2021-05
Pharmaceuticals • Biotechnology • B2B
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.
• Provide management and leadership to plan, prepare, and execute complex and high-profile clinical trial or Regulatory projects and/or programs. • Interface with internal departments and company leadership, and externally with sponsors and vendors. • Drive activities to conclusion with minimal support and mentor team members.
• Bachelor’s degree in life/health sciences or related discipline, or equivalent required. • 5 to 8 years of Project Management experience leading global/complex clinical trials in a Clinical Research Organization/Pharmaceutical Company • Executive level communication, written oral communication, interpersonal skills, strong planning and organizational ability required. • Good working knowledge of drug development process and regulatory requirements, including familiarity with International Conference on Harmonisation (ICH). • Proficiency in English (written and verbal). • Action-oriented and resilient in a fast-paced environment. • Ability to lead high performing cross functional project teams, motivate others, and manage relationships with internal and external team members, including vendors, clients, etc. • Advanced stakeholder communication, escalation problem solving, and decision-making skills.
• Remote working • Flexible time off • Paid holidays • Medical insurance • Tuition reimbursement • Retirement plans
Apply Now🔥 2 hours ago
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