inVentiv Health Clinical, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies, offering therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team.
A leading global CRO company are looking for an experienced Drug Safety Specialist to join the Pharmacovigilance department to work in the QPPV support team. The right candidate for this role will be highly motivated by career progression and have post approval and marketing experience within the EU.
An exciting new opportunity has become available for a Safety Reporting Specialist at a leading CRO company based in the UK. This is a great opportunity to join the company as a PVG Regulatory Submission Specialist. This position will allow you to develop your career at a global level within Pharmacovigilance.
My client, among the top 5 CRO's currently seeks a REGULATORY AFFAIRS MANAGER or DIRECTOR to become the Pharmacovigilance Regulatory specialist within Europe.
This is a PERMANENT role based in South East UK.
If you are interested in this role or hearing more about current vacancies, please do not hesitate to contact Ryan on +44 (0) 203 327 3072 or alternatively send your enquiry/CV to firstname.lastname@example.org
The Local Drug Safety Officer (LDSO) is accountable to ensure full compliance with all relevant global and local regulatory requirements, internal company standards and best practices in the pharmaceutical industry for drug safety management. The LDSO is accountable to ensure the secure functioning of the local PV system in accordance with the global PV system of the company.
At PPD, we are ever expanding. We are looking for candidates to register their interest in joining PPD within our Pharmacovigilance department. We are searching for experienced Safety Specialist candidates to join our Cambridge team only.
Pharmacovigilance Business Systems Analyst - 12 month maternity cover - Hertfordshire
This global pharmaceutical giant, with an excellent reputation, pipeline and known for being a great place to work, is seeking a Pharmacovigilance PV Scientist or Specialist who is interested in pursuing working within business and IT reporting and working with submissions systems.
I am currently looking for an individual who is looking to take the next step in their career and gain some valuable and wider experience. The perfect candidate must have Strong Drug Safety Knowledge and the desire to develop with the business.
An exciting opportunity to join a growing and dynamic company based in the south east as a Pharmacovigilance Officer or a Senior Pharmacovigilance Officer. The company offers a competitive package, clear career development paths and in depth training in areas candidates are interested in developing skills.
Global Director, Drug Safety Standards - Cambridgeshire.
The Company My client, a high functioning research Biopharmaceutical company, is looking for someone to join them at Director level. This company has probably one of the strongest pipelines in the industry and have forecast to submit at least 1 to 2 MAAs each year for the foreseeable future.
Playing a heavy emphasis on science, this company is built on strong scientific research and minds to help push and grow the co
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