Clinical Data Specialist

Summary of the Clinical Data Standards Manager Acts as the functional expert in clinical data standards required by regulatory authorities and industry groups such as CDISC. Supports Clinical Data Managers, Data Management Leads, and the wider Clinical Trial Team to ensure clinical data is complete, accurate, consistent, and ready for regulatory submission....

Join a growing Clinical Data Management team as a Clinical Data Specialist and help shape the future of data integrity in clinical research! R&D Partners is seeking a Clinical Data Specialist to join a leading organization who are continuously growing their Clinical Data Management function. Support the production/QC of various Clinical Data...

PMCF Specialist (Medical Devices / Clinical & Regulatory Affairs) Start Date: ASAP Contract Duration: 12 months (possibility of extension) As a PMCF Specialist, you will join the Clinical and Regulatory Affairs team at a leading global healthcare company’s Medical Devices division in Diegem, Belgium. You will collaborate with cross-functional...

PMCF Specialist (Medical Devices / Clinical & Regulatory Affairs) Start Date: ASAP Contract Duration: 12 months (possibility of extension) Location: Diegem, Belgium Job Description As a PMCF Specialist, you will join the Clinical and Regulatory Affairs team at a leading global healthcare company's Medical Devices division in Diegem, Belgium. In this role,...

Planet Pharma are currently partnered with a global clinical research organisation and we are actively seeking a Senior CRA to join the business on a permanent basis, fully remotely in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted according to protocol, Good Clinical Practice (GCP), and regulatory requirements....

FERTIGA is a pioneering healthcare start-up committed to advancing fertility treatments through cutting-edge molecular testing during IVF (In Vitro Fertilization) treatment. Our flagship product, the Aurora Test, is a groundbreaking analysis of the cells surrounding the egg during ICSI (Intracytoplasmic Sperm Injection) treatments. The test results empower...

Title: Senior Clinical Research Associate Company: Global Leading CRO Location: Remote - Belgium Our client is seeking an experienced CRA II or Senior CRA with strong oncology experience to take full ownership of 1–2 clinical protocols. This role goes beyond traditional monitoring, encompassing contract negotiation, start-up activities, monitoring, and...

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you...

At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Clinical Research Associate II (m/f/d) – The Netherlands or Belgium 18 months to 4 years of site monitoring experience in clinical research ~ Proficiency in documentation, reporting, and data review processes ~ Fluent in Dutch and English; additional...

Clinical Research Associate – Belgium (Home-Based / Hybrid) Chloe O'Shea is partnering with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking a Clinical Research Associate to join a dedicated single-sponsor team in Belgium. This is an exciting opportunity to take ownership of site...