Director Site Management & Monitoring (m/f/d)

At Pfizer we combine scientific excellence with a clear purpose: better health care decisions and better treatment outcomes for patients worldwide. Through evidence-based medical expertise, clear standards and the responsible handling of data, we create trust and orientation – for doctors, partners and patients. In this role, you contribute actively to strengthening medical decisions and promoting the safe, effective use of innovative therapies.

Design clinical research with global impact. At Pfizer we work every day to develop therapies that improve patients' lives in the world. As a Director Site Management & Monitoring (m/w/d), you play a key role in managing and developing our clinical study activities – with strategic responsibility, international cooperation and growing leadership. Your role – Effective & strategic In this position, you are responsible for the Site Management and Monitoring activities in Germany and ensure that clinical trials are conducted qualitatively high-quality, regulatory and efficient. You work closely with global and local stakeholders and actively develop the clinical study environment. A key part of the role is leadership responsibility: You lead and develop Clinical Research Associates (CRAs) as well as further monitoring roles – perspectively with further development of team responsibility. Overview of your tasks Strategic and operational responsibility for Site Management & Monitoring in Germany Professional and disciplinary leadership and coaching of CRAs and other monitoring roles (directly and/or via partners) Ensuring quality, compliance and patient safety according to GCP, regulatory requirements and internal standards Close cooperation with Study Start‐Up, Regulatory, Medical Affairs, CROs and other internal and external partners Developing country and location strategies (e.g. site selection, start-up optimization, risk management) Active participation in strategic initiatives, innovations (e.g. virtual/remote monitoring approaches) and continuous process improvement Presentation of Pfizer in relevant external bodies and networks

Complete studies (e.g. natural sciences, medicine, pharmacy) or a comparable qualification Long-standing experience in clinical research, ideally in an international pharmaceutical or CRO environment leadership experience and joy in the development of employees is desirable Very good understanding of clinical trials, monitoring, quality and regulatory requirements Flowing German knowledge and excellent English skills Representative communication and stakeholder management skills Strategic thinking, strength of decision and a high degree of self-responsibility Standing for occasional missions ‘Breakthroughsthatchangepatients’lives’- Our clear corporate goal is to achieve breakthroughs that change the lives of patients. You are the meaning of our actions.

Pfizer guarantees equal opportunities throughout the entire application process and compliance with local legislation in the respective countries where Pfizer operates. Pfizer excludes any discriminatory factors affecting, inter alia, gender and age, ethnicity, religion or belief, sexual orientation or disability. Inclusion of people with disabilities Our aim is to enable all employees to complete and develop their skills and knowledge. We are proud to be an inclusive employer by offering equal opportunities to all applicants. We encourage you to show off your best page with the knowledge and confidence that we will make all reasonable adjustments to support your application and your future career. Your journey with Pfizer starts here! Medical