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 Biotechnology, Clinical Research and Pharmaceutical organization, based in Netherlands.
They are a global research organization which strives for quality and has offices in almost 50 countries. They provide management services, integrated drug development and laboratory and lifecycle management services.
ROLE DESCRIPTION
Currently we are looking for a talented and ambitious Clinical Resource Associate. You will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Standard Operating Procedures.
RESPONSIBILITIES
Your responsibility is to perform and coordinate all aspects of the clinical monitoring and site management process. You will ensure that data will pass international quality assurance audits. You will represent de organization in the global medical research community and develop and maintain collaborative relationships with investigational sites and client company personnel. Further you’ll be involved in:
- Assisting the project manager or clinical team manager on assigned projects
- Support line manager
- Travel 60-80% on average
REQUIREMENTS
- BSc/MSc in a science related field
- +- 5 years experience in Clinical research with a high level of expertise in clinical monitoring
- Knowledge of FDA guidelines, GCPs and applicable Standard Operating Procedures
- Skills to mentor and train other monitors in a positive and effective manner
- Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology
- Excellent organizational and time management skills
- Effective presentation skills
- Ability to utilize problem-solving techniques applicable to constantly changing environment
- Fluent in English and 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.
