
Project Director – Neurology, Immunology, Infectious Diseases
Posted 11 hours ago

Posted 11 hours ago
This is a fully remote position, open to applicants in United States.
• Accountable for the overall quality and management of clinical trial project deliveries and associated programs.
• Manages intricate, cross-functional resource needs in accordance with budget, timelines, scope, and quality expectations for project completion.
• Oversees financial budgets, ensuring accurate forecasting, planning, invoicing, and timely execution of out-of-scope activities.
• Reviews and approves proposal content and associated costs.
• Ensures effective risk management throughout the project delivery lifecycle.
• Negotiates and influences both internal and external team members in a professional manner to achieve successful outcomes.
• Effectively resolves problems within project teams by utilizing strategic thinking and conflict resolution skills.
• Balances multiple competing priorities while ensuring effective and efficient resource utilization across projects and programs.
• Acts as the primary contact for assigned clients regarding scope delivery, customer satisfaction with services and capabilities, and assessment of client needs.
• Demonstrates knowledge and insight into general business principles and practices, effectively balancing business priorities.
• Exhibits a growth mindset and approaches complex challenges with creativity and adaptability.
• Leads by example, encouraging team members to develop robust solutions for clinical trial delivery.
• Assists in the recruitment and interviewing processes for new employees.
• Responsible for supervising project staff and communicating with functional managers, including providing performance feedback.
• This position requires 10% business travel, which may include international travel.
• A minimum of a Bachelor’s degree in life sciences, healthcare, or business; a Master’s degree or higher is preferred.
• At least 7 years of relevant work experience.
• Minimum of 7 years of experience in drug development and/or clinical research.
• Extensive experience in clinical project management, with no less than 5 years in that role.
• Candidates with Clinical Research Associate (CRA) experience are preferred.
• Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and relevant local regulatory requirements.
• Strong financial acumen, administrative competence, and analytical abilities.
• Experience in managing global clinical trials.
• Exceptional written and verbal communication, planning, critical thinking, and organizational skills, including a strong command of the English language.
• Proficiency in various applications, including but not limited to Microsoft Word, Excel, and PowerPoint.
• Expertise in the clinical trial delivery process.
• Strong general administrative skills and experience.
• Outgoing and client-focused.
• Proactive and solution-oriented.
• Strong presentation and networking skills.
• Experience in applying a data-driven approach to enhance clinical trial delivery solutions.
• Comprehensive benefits package tailored to location.
• Competitive salary structures based on location.
• Departmental Study/Training Budget to promote professional development.
• Flexible working hours (within reasonable limits).
• Opportunity for remote/hybrid work arrangements depending on location.
• Leadership and mentoring opportunities available.
• Participation in our Buddy Program for new or existing employees.
• Internal growth opportunities and pathways for career progression.
• Financially rewarding internal employee referral program.
• Access to online soft skills and technical training through GoodHabitz and other internal platforms.
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