Why Syneos Health? Join a game-changing company that isreinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 23,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options.
Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings.
This expertise, combined with our Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-
how to help our clients with every facet of their Oncology research.
We are currently looking to strengthen our Clinical Monitoring team in The Netherland and are seeking a CRA or senior CRA for our Oncology Business Unit.
This role may be home-based or office-based in Amsterdam in our office with a beautiful view. Also, a lot of colleagues are combines office-
and home-work. A summuray of duties you will be involved in; - Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures-
Data Handling, Reporting and Tracking & administrative tasks - You would also perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines
We are looking for an enthusiastic colleague with relevant practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO.
Of course you have a thorough understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines. Fluency in Dutch is mandatory.
Are you enthusiastic about this role? We would be more than happy to speak with you over a cop of coffee! You can directly apply online or contact us via