Senior Regulatory Project Manager

Reading, Berkshire
Closing date
18 Sep 2020

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Regulatory Affairs, Project Management, Regulatory Project Management
Full Time
Contract Type
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Bayer has an exciting new career opportunity for a Senior Regulatory Project Manager within the Pharmaceutical Division based in our Reading offices. In this new role you will provide regulatory strategic leadership and support for our Oncology portfolio and will be part of the Regulatory Policy and Intelligence Network concentrating on Europe.

Bayer is a global Life Science Company concentrating on the Healthcare and Nutrition sectors, with a vision for the future that promises health for all and hunger for none. In the Pharmaceutical Division, Bayer is committed to innovative scientific research and discovery, and guided by our purpose of Science for a Better Life, aim to improve patient’s lives by giving science meaning, and translating our research into solutions that make their lives better. As part of our commitment to serving patients, we aspire to become leaders within the Oncology field, and through our policy work to ensure Europe remains at the forefront of innovation.

We operate in a strong global network building on our business acumen, analytical skills and regulatory knowledge to advise our internal partners and negotiate with external stakeholders.


Key Responsibilities

  • Producing high-quality marketing authorisation, variation and clinical trial applications in line with UK/EU requirements.
  • Delivering innovative regulatory strategies and promoting awareness of regulatory requirements.
  • Managing regulatory challenges and pro-actively highlighting impact of external changes
  • Contributing to UK / EU Regulatory Policy by assessing the external regulatory environment and communicating it to the internal organisation.
  • Participating in external EU/UK committees/working groups.
  • Supporting UK Regulatory team development by being an ambassador for the UK team.


Basic Qualifications

  • Bachelors or advanced degree in appropriate scientific discipline
  • Experienced UK / EU regulatory professional having managed major submissions and approvals via the Centralised Procedure, preferably in oncology  
  • Sound knowledge of clinical trial requirements, particularly in major EU countries
  • Ability to think strategically, sound commercial awareness and good knowledge of medicines development within EU
  • Excellent communication skills including proven ability to influence by persuasion and negotiation. Ability to communicate complex information in an engaging manner, both verbally and in written form. Presentation skills are a key communication vehicle for networking within and outside the organisation. 
  • Ability to thrive in and foster strong matrix team working in a global environment

Bayer is a Life Science company with a more than 150-year history and core competencies in the areas of health care and agriculture. With our innovative products, we are contributing to finding solutions to some of the major challenges of our time.

A growing and aging world population requires an adequate supply of food and improved medical care. With our innovative products, we are contributing to finding solutions to some of the major challenges of our time. With life expectancy continuing to rise, we improve quality of life for a growing population by focusing our research and development activities on preventing, alleviating and treating diseases. We are also making an important contribution to providing a reliable supply of high-quality food, feed and plant-based raw materials.

Our goal is to create value for our customers, stockholders and employees, while also strengthening the company’s earning power. We are committed to operating sustainably and addressing our social and ethical responsibilities. Employees with a passion for innovation enjoy excellent development opportunities at Bayer. All this goes to make up our purpose:

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  • United Kingdom
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