Regulatory Affairs Director- Generic Pharma Spain My client are looking for a Head of Regulatory to assist with their expansion and continued growth. Focussing on Generics throughout Europe, you will be in strategic role responsible for the whole EU regulatory and drug safety department Based in the beautiful city of Barcelona, this is Categoría: trabajo en Calidad e I+D / Subcategoría: trabajo en Investigación y desarrollo...

Regulatory Affairs Director Generic Pharma Spain My client are looking for a Head of Regulatory to assist with their expansion and continued growth. Focussing on Generics throughout Europe, you will be in strategic role responsible for the whole EU regulatory and drug safety department Based in the beautiful city of Barcelona, this is an excellent international location with a strong historical background. Normally a holiday destination, this will offer you the chance for an excellent work/life ...

Just Pharma are currently working on behalf of a leading company in the pharmaceutical industry looking for experienced Clinical Research Associates to join their team. These positions offer a very competitive salary long with excellent benefits. The key responsibilities of a Clinical Research Associate (CRA) are to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations, performing clinical on-site monitoring activities, collecting regulat...

Clinical Monitoring Associate ( CMA ) Madrid, Spain Permanent, full-time, office-based. An exciting opportunity to join one of the biggest and most prestigious CROs as a CMA. Clinical Monitoring Associate / II ( CMA / CMA II ) Madrid, Spain Our client - one of the top 5 CRO - is looking to strengthen their team and hire new Clinical Monitoring Associate ( CMA ) to join their fast-growing team. This would be a perfect opportunity for an experienced administrator ( CTA, CMA) or an ambitious CRA se...

PharmaNet/i3 is a drug development services company with a global infrastructure that allows us to conduct any clinical trial, from a single local study to programs spanning multiple continents. For pharmaceutical, biotechnology, generic drug, and medical device companies of all sizes around the world, PharmaNet/i3 works for you For more information, visit http://www.pharmanet-i3.com Senior Clinical Data Manager - Spain As a Senior Clinical Data Manager at PharmaNet/i3 you will lead the data man...

The opportunity to join a world-leading pharmaceutical company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development. Responsibilities include: • all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties • all aspects of site and registry management...

The opportunity to join a world-leading pharmaceutical company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development. Responsibilities include: • all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties • all aspects of site and registry management...

The opportunity to join a world-leading pharmaceutical company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development. Responsibilities include: • all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties • all aspects of site and registry management...

The opportunity to join a world-leading pharmaceutical company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development. Responsibilities include: • all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties • all aspects of site and registry management...

For a confidential consultation call Beatriz de Luis on 0044 (0) 207 255 6665 or email your CV to beatriz.deluis@secpharma.com Job Summary: My client, growing global pharmaceutical company, is currently looking for an EU Senior Regulatory Affairs Manager to join its team in Madrid. For a confidential consultation call Beatriz de Luis on 0044 (0) 207 255 6665 or email your CV to beatriz.deluis@secpharma.com Job Summary: My client, growing global pharmaceutical company, is currently looking for an...