Senior Project Manager

🔥 15 minutes ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $128k - $140k / year

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

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Veristat

WebsiteLinkedInAll Job Openings

501 - 1000 employees

💼 Consulting

🏥 Healthcare

💊 Pharmaceuticals

💰 Private equity on 2021-05

Consulting • Healthcare • 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.

📋 Description

• 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 • Interface externally with sponsors and vendors • Lead high-performing cross-functional project teams • Motivate others and delegate responsibilities • Manage stakeholder communication, escalation, problem solving, and decision-making • Build and manage relationships with internal and external team members, vendors, and clients • Drive activities to conclusion with minimal support • Mentor and delegate

🎯 Requirements

• 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 • Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis • Executive-level communication, written and oral communication, interpersonal skills, planning, and organizational ability • Good working knowledge of the drug development process and regulatory requirements • Familiarity with International Conference on Harmonisation (ICH) guidelines and other applicable regulatory rules and guidelines • Proficiency in English, written and verbal • Ability to lead high-performing cross-functional project teams, motivate others, and delegate • Advanced stakeholder communication, escalation, problem-solving, and decision-making skills • Ability to build and manage relationships with internal and external team members, vendors, and clients • Ability to drive activities to conclusion with minimal support • Ability to mentor and delegate

🏖️ Benefits

• Applicable bonus • Remote working • Flexible time off • Paid holidays • Medical insurance • Tuition reimbursement • Retirement plans