For our client in Basel, we are looking for a Clinical Development Director (CDD).
- Do you have +6 years of experience in clinical research from phase I tot IV?
- Are you good at stakeholder management?
- Are you fluent in English and eligible to work in Switzerland?
- Do have oncology experience?
Then this could be your next step. It would be my pleasure to give you more information (nele_daems@oxfordcorp.com or 0032 15 211 104)
For our clients in Switzerland, France, Germany and other European countries, we are proactively looking for experienced SAS Programmers.
- Do you have a University Degree in Mathematics, Life Sciences, Biostatistics or Computer Sciences?
- Do you have minimum 8 years of experience in SAS Programming within the pharmaceutical sector?
- Do you have expertise in CDISC Standards (SDTMs, ADaM) ?
- Are you fluent in Engish?
Then you are the new colleague we are looking for! Read more and apply as soon as you can!
For one of our clients located in Germany (Goettingen), we are looking for a FREELANCE Cell Culture Media Expert .
- Do you have knowledge about Cell Culture Media Market?
- Do you have knowledge about manufacturing of Cell Culture Media?
- Do you have knowledge about quality requirements for Cell Culture Media in general?
Then do not hesitate to contact me!
We are looking for several physicians the following months to work in Basel at a pharmaceutical company.
- Do you have a qualified medical doctor degree?
- Do you have at least 8 years of experience in clinical research?
- Do you have experience with pulmonology and cardiology?
Then don't hesitate to contact me soon!
For one of our clients, a vibrant science and technology company, we are actively looking for a Project Manager Aggregate Reports in Global Patient Safety Operations (M/F).
If you...
- Have a University degree in life science or vocational qualification as a Healthcare Professional ;
- Have minimum 2 years’ experience in drug safety/pharmacovigilance processes, including safety project management and managing aggregate safety reports ;
- Have an excellent knowledge of spoken and written English (including medical terminology) - a good knowledge of German is an advantage.
Then you might be the candidate we are looking for! Don't wait anymore and send your application today!
For one of our clients located in Switzerland (Lausanne), we are looking for a Senior Clinical Trial Associate.
- Do you have a University/College degree level or equivalent in a relevant discipline?
- Do you have at least 5 years of experience as CTA or comparable operating experience in Pharma/CRO/healthcare with good knowledge of budget and invoicing requirement, as well as drug development process and medical terminology?
- Are you fluent in French and in English ?
Then, you might be the candidate that we are looking for.
Our client in Lausanne, Switzerland, is looking for an experienced Clinical Data Manager to join their teams.
Do you...
- Hold a Master Degree ?
- Have approximately 5 years of experience in clinical data management, with strong experience using major EDC systems and related tools and technologies ?
- Have a fluent English level - written and spoken ?
Then, this might be the next step in your career !
For one of our clients located in Amsterdam, we are actively looking for an experienced Clinical Site Manager / CRA.
Do you...
- Have a Bachelor or a Master (biological science, pharmacy or other health related discipline) ?
- Demonstrate a substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology ?
- Speak English fluently and have a good knowledge of French and/or Dutch ?
Then, this is the next step in your career !
Pour l'un de nos clients situé dans le nord de la France, nous sommes activement à la recherche d'un Junior Regulatory Compliance Specialist.
- Etes-vous Pharmacien ou diplômé d'un Master Scientifique?
- Avez-vous une première expérience en industrie pharmaceutique?
- Avez-vous un bon niveau de Francçais et d'Anglais?
Alors, vous êtes probablement notre futur collègue.
For one of our clients we are looking for a QA Associate III.
- Do you have a CMO Management qualification?
- Do you speak fluent English?
Then you might be the candidate we are looking for !
Valesta seleeciona para importante laboratorio en Madrid, un Técnico de Farmacovigilancia con experiencia mínima 3-4 años en sector farmaceutico. La contratación es indefinida.
Se solicita Licenciado / Graduado, postgrado valorable y nivel de inglés muy alto.
Funciones: gestión de sospechas de reacciones adversas, manejo de BBDD, revisión de búsquedas bibiliográficas, notificación de sospechas de reacciones adversas, formación en Farmacovigilancia al personal de la compañía, revisión y actualización de procedimientos, revisión y seguimiento de los planes de gestión.
We are regularly looking for Medical Doctors with experience in the pharmaceutical industry.
We regularly have vacancies for clinical research physicians, and within medical affairs. This in several European countries such as Switzerland, Germany, France, Belgium and the Netherlands.
Don't hesitate to contact us, should you be interested in finding out more on career options and vacancies.
