Project Manager Associate
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 Groningen Netherlands.
The company is a big CRO which deals with clinical trials in every stage. Our client is an International player with only in the Netherlands more 150 employees.
ROLE DESCRIPTION
As an Associate Project manager you are responsible for the organisation, coordination an analysis of the clinical studies. You will work under the guidance of a Project Manager and provides the necessary support on both administrative and coordinating levels within the projects. In addition, maintaining good customer contacts is a crucial aspect of this feature.
RESPONSIBILITIES
- Ensure that study team members are aware of budget requirements.
- Inform Project Managers of deviation from budget, timelines, resource, or potential out-of-scope activities.
- Work in a timely manner in accordance with the agreed budget, under the supervision of the Project Manager. T
- Take on project management tasks as delegated by the Project Manager.
- Fulfill PM duties in the absence of the PM
- Function as a point of contact for Clinical Operations colleagues
- Coordinate implementation and maintenance of Clinical Project Management System
- Ensure that submission documents are prepared per local requirements in conjunction.
- Conduct all activities according to defined project-specific quality and performance standards as well as relevant SOPs, ICH GCP
REQUIREMENTS
- MSc in a science related (pharmaceutical) area
- 3 years of experience
- Fluent in English
- Fluent in Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Romy van Ooijen.
