Belgium, Clinical Trial Regulatory Leader - Senior RA_PD_13544-MZ
Here is a chance to join one of the most globally known pharmaceutical organisations, who is looking to hire a Clinical Trial Regulatory Leader based in Beerse, Antwerp. This job will be working a top 10 pharmaceutical company that works across a range of industries from medical devices to pharmaceutical and consumer goods, operating in over 60 countries.
The Clinical Registry is responsible for posting accurate, validated and consistent information about our trials and their results on about 40 registries globally. The CR directly maintains clinicaltrials.gov and posts results on EudraCT. The CR oversees and supports all other regional or country specific registries. The CR is the centre of expertise for disclosure requirements and ensures data quality and compliance requirements for all registries are met. The CR is based in the company BRQC, but supports all pharma, consumer and medical devices operating companies that have studies with disclosure requirements. We work closely together will clinical and medical teams, clinical development operations, regulatory affairs, bio stats, programming, and local operating companies to ensure the company meets its disclosure requirements. Through collaboration with other BRQC departments and IT we ensure complete and high-quality data is available for timely disclosure of all required studies. The CR team is in the US and EU and part of the work is performed in an offshore model in India. Because of expansion of our scope and growth of the trial portfolio, we are recruiting for an additional clinical registry senior specialist, international registries.
Please visit our website at www.proclinical.com