Job Opportunities in Poland


September 20, 2024

Merck Group

Warszawa

OTHER


Associate Director, Clinical Trial Lead (all genders)


Work Your Magic with us!


Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.



United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.


This role can be done in a fully remote working model.
Your role:
The new hire will manage multiple studies, projects, and work streams with high complexity, risk, impact and reach, typically Ph III and registrational/sourcing models. You will lead the development of the clinical trial strategy while accountable for successful project execution and delivery of clinical operational budget, timelines and quality standards agreed upon by Governance Committees. As a core member of the Clinical Operations Team and leader of the Clinical Trial Team, you align clinical trial team with organizational goals, Clinical Operations Team, and/or Global Program Strategy Team. You will filters, prioritizes, analyzes and validates complex and dynamic information from a diverse range of external and internal sources to respond to operational and organizational challenges in a holistic manner to mitigate risks.
You will be acting as a senior advisor and mentor within the team and beyond and serves as best practice resource within own discipline or as technical functional teams or projects. Ensuring all study management activities will be completed in accordance with SOPs/WI, local regulatory guidance including ICH-GCP; audit leadership- interviewee & responses. You will also contribute to non-study -related initiatives in addition to study assignments. Provide reports to senior management, including updates and timelines independently. To be sucessfull in this role you would demonstrate skills in successfully leading large-sized global project teams in a matrix organization and directs, influences and motivate stakeholders from closely related areas and beyond, create a positive working climate, trate creativity and innovation to support projects from a strategic perspective, able to predict the result of action in advance and achieve goals.

Who you are:
  • At least 10-12 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 7 years of in-depth experience in clinical trial management including managerial responsibility. Advanced degree desirable (MPH, MS, MA, MBA, Pharm D); PM c PMP) desirable.
  • Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing study activities, from startup through final study report.
  • Experience in multiple Therapeutic Areas (oncology and immunology preferred)
  • Requires substantial to extensive professional experience in relevant disciplines and substantial project management experience. Required and experience in own discipline and beyond which may also require good market and competitor knowledge.
  • Strong leadership competencies and influencing skills, proven team dynamic knowledge and skills and ability to foster partnerships across projects and multidisciplinary teams.
  • Growing expertise in drug development, including some knowledge of interfaces and interdependencies of clinical development with other nonclinical & pharmaceutical development, regulatory, commercial/marketing)
YOUR MAIN BENEFITS:
  • Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card
  • Work-Life balance: Enjoy additional paid days off, flexible working hours.
  • Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
  • Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.
Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!


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