project manager for clinical research

Enfint; Warszawa; On-site; PLN 240,000 - 420,000; Full time

Benefits offered by this job

Annual bonus 20%

Medicover

MultiSport

UNIQA

Company car

Job summary

Pfizer ищет опытного руководителя программ клинических исследований, способного координировать внешних партнеров, исследовательские площадки и команды по всему миру. Кандидат будет ответственен за планирование, управление рисками, бюджеты и соблюдение регуляторных требований.

Требуется сильный опыт в клинических операциях, постановке задач, общения с стейкхолдерами и управлении множеством исследований. Привлекательные бонусы, Медиковер и прочие льготы.

Qualifications

• Требуется высшее образование в сфере, смежной с фармацевтикой или науками
• 7+ лет опыта в фармацевтике/ клинико-исследовательской деятельности
• Знание GCP, мониторинга, клинических и регуляторных операций
• Умение управлять проектами и лидировать
• Опыт работы с подрядчиками и вендорами
• Умение оценивать и presents сложные данные и риски
• Наличие письменной и устной коммуникации на высоком уровне
• Плюсом будет PMP и глобальный опыт

Responsibilities

• Р oversee внешних исследовательских сотрудников, партнеров и органов.
• Продвижение оперативной эффективности и обмен лучшими практиками.
• Управление планированием, рисками и коммуникациями внутри проекта.
• Управлять портфелем исследований и руководить Study Managers.
• Проводить встречи команд и фиксировать протоколы и действия.
• Анализировать предложения о сотрудничестве и вести их в систему.
• Контролировать юридическую и финансовую часть проектов, включая бюджет и график.

Skills

English fluency

Communication skills

Project management

Leadership

Vendor oversight

Data interpretation

Analytical thinking

AI familiarity

Education

Bachelor’s degree

Master’s degree (желательно)

Tools

Microsoft Office

PMP (сертификация)

Job description

Описание

Pfizer is a pharmaceutical company focused on developing medicines and transforming patients’ lives. Its digital transformation strategy applies data, modelling, and automated solutions to drug discovery and development.

Задачи

• Oversee therapeutic areas engaging with external research collaborators, investigators, academic organizations, government agencies, pharmaceutical companies, alliance partners, and vendors
• Champion operational excellence, continuous process improvement, and global sharing of best practices
• Lead planning, risk management, internal and external communications, and stakeholder management
• Manage a portfolio of studies and oversee Study Managers
• Lead internal and external study team meetings and capture minutes and actions
• Review and classify research collaboration proposals and enter information into the research collaboration system throughout the study lifecycle
• Oversee internal due diligence and ensure completion by appropriate subject matter experts
• Lead due diligence meetings and monitor action items and decision-making
• Facilitate development of research collaboration agreements, budgets, and study plans
• Develop and maintain integrated program-level budgets and updated forecasts
• Ensure alignment on asset strategy, milestones, and interdependencies
• Develop and monitor timelines, milestones, and risk mitigation strategies
• Ensure appropriate resourcing and elevate concerns as needed
• Collaborate with internal and external partners and stakeholders
• Respond to leadership and stakeholder queries about proposals, studies, policies, and procedures
• Serve as the primary operational contact for external collaborators, research sites, cooperative groups, and global networks
• Consult with drug and regulatory subject matter experts on collaboration strategies
• Facilitate development of study-related documents, including protocols and ICDs
• Facilitate creation of contracts and amendments with Legal and lead negotiations as needed
• Identify and manage emerging changes and opportunities and update project schedules
• Manage study progress reports and results, recommend corrective actions or study termination for non-performance
• Monitor operational efficiency, timelines, scope, and budget
• Identify and manage compliance risks and oversee compliance within the assigned therapeutic area
• Ensure completion of study closure activities
• Monitor process and training needs
• Assist with curriculum development and training on operational strategies and compliance regulations
• Adhere to applicable SOPs, standards, working practices, and implementation guidelines and contribute to their development
• Train and mentor Study Managers, medical and clinical leads, and subject matter experts
• Communicate team roles and responsibilities, support onboarding, and ensure access to necessary project information
• Ensure appropriate team member views are acknowledged and incorporated into decisions

Требования

• Bachelor’s degree
• 7+ Years of experience
• Applicable pharmaceutical industry experience
• Working knowledge of Good Clinical Practices, monitoring, clinical, and regulatory operations
• Demonstrated project management and leadership experience
• Experience with vendor oversight
• Ability to evaluate, interpret, and present complex issues and data to support risk
• Excellent written and verbal communication skills
• Fluent English
• Effective decision-making, analytical, and solution-oriented approach
• Proficiency in Microsoft Office Suite and familiarity with AI
• Nice to have: Master’s degree, advanced education or training/experience, contract development and management experience, multidisciplinary matrix team experience, change management experience, PMP certification, pharmaceutical industry experience, global clinical study management experience

Условия

• Annual bonus: 20%
• Medicover
• Multisport
• UNIQA
• PPE at Goldman Sachs
• company car
• other benefits under Pfizer Pay Policy