Senior Clinical Research 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 Clinical Research organization, based in Netherlands.
They're a well known company with an enormous amount of therapeutic areas. They have worked on over 80+ marketed drugs all over the world. They got an FDA regulatory approval over half of those drugs. The company success is created around the idea to surround themselves by talented professionals and this really works out for them. They got over 7500 employees who come from all around the globe.
ROLE DESCRIPTION
You will provide innovative solutions for the clients. Working completely outsourced to and based at offices of the global clients you will be responsible for management of investigator sites throughout a lifecycle. Working with ICH-GCP guidelines and study protocol. You'll foster relationships with investigator site staff and ensure clinical metrics are met.
RESPONSIBILITIES
Establishing innovative ways to increase site and patient recruitment, you will be working project based and when issues occur you proactively implement actions plans. A very creative twist of the job; when interested you may design and deliver training to the staff. Other responsibilities and activities you will be working on include:
- Preparing for and attending investigator meetings, coordinate those meetings
- Ensure integrity of clinical data by maintaining site track records
- Drug development process of the client
REQUIREMENTS
- 4-6 years of prior experience in a related function in the pharmaceutical industry
- MSc in a science related field
- Working knowledge of ICH-GCP guidelines
- Knowledge of International Regulatory Requirements
- Fluent in Dutch and English
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.