Clinical Data Reviewer — Medical Affairs

Make your mark for patients We are looking for a DT Lead Medical Affairs who is strategic, collaborative, and results-driven to join us in our Digital Technology Patient Evidence team, based in our HQ office in Brussels, Belgium. About The Role In this global role, you will lead the digital technology strategy and delivery for Medical Affairs systems...

EPM Scientific are currently partnered with a leading Medical Device organisation conducting international clinical research programmes across Europe. They are seeking a Clinical Research Associate to support ongoing and upcoming clinical studies. This individual will play a critical role in overseeing clinical study sites, ensuring high-quality data...

For our client, a global medical device company, we are looking for a Clinical Research Associate. Position Summary The Clinical Research Associate (CRA) is responsible for monitoring and overseeing clinical investigations involving medical devices to ensure compliance with applicable regulations, Good Clinical Practice (GCP), study protocols, and company...

## Medical Affairs and Evidence Generation Asset Lead –Executive DirectorApply: Belgium - Remote: Switzerland - Remote: Full time: Posted Today: REQ-4573*Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a...

Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCPAssist with or oversee study...

For our client, a global medical device company, we are looking for a Clinical Research Associate.Position SummaryThe Clinical Research Associate (CRA) is responsible for monitoring and overseeing clinical investigations involving medical devices to ensure compliance with applicable regulations, Good Clinical Practice (GCP), study protocols, and company...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Regulatory Affairs Associate Director- Labeling strategist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the...

As a Clinical Research Associate, you will be responsible for managing clinical study activities across multiple study sites within one or more clinical projects for the MedTech group. You will play a key role in ensuring the successful execution of clinical trials, maintaining high-quality data collection, and safeguarding the safety and well-being of study...

At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.Job DescriptionIf you’re looking for a meaningful job with a dynamic...