Senior Project Manager

August 14

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Veristat

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Biotechnology • Pharmaceuticals • Science

Veristat is a specialty Contract Research Organization (CRO) that offers comprehensive clinical trial and consulting services. Particularly focused on the pharmaceutical and biotechnology sectors, Veristat supports their clients' development and regulatory strategy for complex and novel therapies. The company's expertise spans biologics, gene therapies, rare diseases, and regulatory submissions. Their services include full-service clinical trial planning, clinical trial conduct, and regulatory affairs, with a strong emphasis on adaptive designs, biostatistics, and pharmacovigilance. Veristat has been pivotal in advancing therapies through strategic consulting and clinical operations, from oncology and neurology to infectious diseases.

501 - 1000 employees

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

💰 Private Equity Round on 2021-04

📋 Description

• The Senior Project Manager provides management and leadership to plan, prepare, and execute multiple complex and high profile projects. • Interfaces with clinical monitoring and site management, clinical data management, SAS programming, biostatistics, pharmacovigilance, and medical writing. • Interfaces internally with business development, corporate compliance and company leadership, and externally with sponsors and external vendors. • Veristat highlights: 30+ years of expertise accelerating life-changing therapies; 105+ approved therapies for marketing applications; 480+ oncology projects; 350+ rare disease projects. • Flexible, inclusive culture — 70% remote workforce; 66% women-led teams.

🎯 Requirements

• Bachelor's degree in life/health sciences or related discipline, or equivalent required. • 6 to 8 years of relevant clinical research experience in a Clinical Research Organization/Pharmaceutical Company, with a minimum of 3 years of Project Management experience in a CRO or pharmaceutical company required. • Familiarity with International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research. • Excellent clinical trial project management, written and oral communication, organizational, and interpersonal skills are required. • Proficiency in English (written and verbal). • Action-oriented and resilient in a fast-paced environment and will have the ability to build and lead effective project teams, motivate others, delegate, and make and implement decisions. • Ability to build and maintain trust and confidence and communicate effectively with client, external vendors, and internal team members. • Ability to mentor and delegate.

🏖️ Benefits

• Flexible, inclusive culture • 70% remote workforce • 66% women-led teams