Senior Clinical Trial Manager
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Noord-Holland Netherlands.
The company is expanding and looking for a clinical trial manager.
ROLE DESCRIPTION
You will oversee clinical studies on a global level.
RESPONSIBILITIES
- Overall study management of global clinical trials to time, budget and quality from a Clinical Operations perspective
- Leadership of the global clinical team and support in their daily business
- Ensure successful and high quality delivery of the study in accordance with ICH/GCP and other regulatory requirements
- Point of contact for the client, internal study team and where appropriate sites to ensure all contractual trial activities are met
- Creation and implementation of a study performance reporting tool
- Responsible for the strategic oversight of all clinical activities
REQUIREMENTS
- University Degree in Life Science/ related field of study or equivalent combination of studies, nursing qualifications, and/or work experience.
- At least six years of experience
- Very good understanding and experience in clinical study management, monitoring, developing study related documents, associated regulatory, processes and quality requirements
- English and Dutch are a must.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
