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South East - UK
Company: PDR PartnersSalary: On Application
Market Applications and post-market variations, execution of CMC specific issues for expansion strategy... in international markets, identification of local agents to liaise with local regulatory authorities and developing... , clinical and CMC aspects and a detailed understanding of regional regulatory problems and strategic... mngr South East UK CMC submissions
Requirements: Our Client is looking for a Senior Manager in Regulatory Affairs with experience of registration of regulated products in Emerging Markets. Joining the International Expansion team within the Regulatory Affairs division, this Senior Manager
Jobs similar to "cmc markets": emerging markets manager
Switzerland
Salary: 160,000CHF
Regulatory Affairs Manager / French speaking Switzerland / Global CMC Biotech roleLocation... :SwitzerlandMy Client is a Global organization that develops, manufactures and markets products that save... and biotechnology to products. Their office in Switzerland is seeking a highly skilled CMC regulatory specialist
Contract: Permanent
South East
Company: Clinical ProfessionalsSalary: Negotiable + Benefits
will be accountable for overseeing and interpreting RA CMC expectations in new markets, advising teams on appropriate... post-approval CMC applications in the EU and/or in International (emerging) markets. * Preferably, RA... Regulatory Affairs CMC Manager Regulatory Affairs CMC Manager The Company Our client is a leading... one of the best corporate employers in the UK. They are currently looking for a Regulatory Affairs CMC
Salary: On Application
and cover European and main International Markets. This is still a growing department and the company continues to build on past and present success. You will receive a very competitive salary with full benefits package, gym... / Regulatory Executive / Regulatory Officer / Regulatory Operations / CTA / CTA`s / Clinical Trials Application / Centralised procedure / CRP / Clinical / CMC / MRP / Mutual Recognition Procedure / Drug development / Pharmaceutical
Requirements: Regulatory Affairs Senior Executive - Gain Centralised and Decentralised Submissions experience – Excellent salary – great career growth available. Location: Hertfordshire, In the first instance please call Jason, Matt or Theo on +44(0)207 697 7300 or +44
Salary: On Application
of NCEs, throughout the EU and International Markets; Portfolio responsibility for major Pharmaceutical products focusing on National and European regulatory activities, including multi-disciplinary product development activities... / CTA / CTA`s / Clinical Trials Application / Centralised procedure / CRP / Clinical / CMC / MRP / Mutual Recognition Procedure / Drug development / Pharmaceutical Development / Biological Development / Manufacturing / Pre
Requirements: Senior Regulatory Affairs Executive / Become an EU Project Mgr / Essex, Location: Essex, London, Cambridge, Hertfordshire, In the first instance please call Jason, Matt or Theo on +44(0)207 697 7300 or +44 (0) 7918 649 405 or please send a full CV to CV@a
Basel, Neuchatel, Geneva, Allschwil, Zurich
Company: Advanced Regulatory (EU Roles)Salary: Negotiable
My client is seeking an experienced Regulatory Affairs professional to provide full regulatory support across European markets by preparing/reviewing/executing regulatory strategies for the development, registration... . • Define submission plans (including timing for CTA or amendments and HA reporting requirements; CTD submission dossier content, scope and timing). • Provide input into Pre-Clinical, Clinical, and CMC about the feasibility of local
Requirements: Would you like to work in Switzerland and beat the Downturn? ** Switzerland / Regulatory Affairs Associate Director / Define & Execute clinical RA strategies,** Location: Europe, Switzerland, Zurich, Basel, In the first instance please call Jason, Matt or
Basel, Neuchatel, Geneva, Allschwil, Zurich
Company: Advanced Regulatory (EU Roles)Salary: Negotiable
in the interaction with EU regulatory agencies during product lifecycle management • Gives regulatory input to ensure acceptable labelling in EU markets. • Prepares EU regulatory submissions in collaboration with the other disciplines... / Regulatory Operations / CTA / CTA`s / Clinical Trials Application / Centralised procedure / CRP / Clinical / CMC / MRP / Mutual Recognition Procedure / Drug development / Pharmaceutical Development
Requirements: *Switzerland* Regulatory Affairs DRA Manager / Switzerland / Use your CTA exp to Gain Centralised Procedure exp, Location Switzerland, Basel, Neuchatel, Geneva, Allschwil, Zurich, In the first instance please call Jason, Matt or Theo on +44(0)207 697 7300
Basel, Neuchatel, Geneva, Allschwil, Zurich
Company: Advanced Regulatory (EU Roles)Salary: Negotiable
, guidelines, procedures etc. • Takes the lead in the interaction with EU regulatory agencies during product lifecycle management • Gives regulatory input to ensure acceptable labelling in EU markets. • Prepares EU regulatory... / CRP / Clinical / CMC / MRP / Mutual Recognition Procedure / Drug development / Pharmaceutical Development / Biological Development / Manufacturing / Pre-Clinical / Phase 1 / Phase 2 / Phase 3 / MAA / Marketing Authorisation
Requirements: Regulatory Affairs DRA Manager / Switzerland / Use your CTA exp to Gain Centralised Procedure exp. Location Switzerland, Basel, Neuchâtel, Geneva, Allschwil, Zurich, In the first instance please call Jason, Matt or Theo on +44(0)207 697 7300 or +44 (0) 79
South East
Company: Blue Heron PharmaceuticalSalary: On Application
of product registration and lifecycle management for international markets. Working with a variety... of International Market Applications for new products and post-marketing variations (labelling & CMC). You... as experience in license maintenance regulatory submissions in international markets. To have a general
Requirements: Major pharmaceutical company planning international expansion requires additional regulatory resource for 2010. To join a 30-strong team based in the UK to support international regulatory affairs.
South East
Company: Blue Heron PharmaceuticalSalary: On Application
registration and lifecycle management for international markets in "emerging" countries, i.e. countries other... (labelling & CMC). You will be seen as a custodian of regional requirements & approval processes and may have... submissions in international markets. To have a detailed understanding of regional regulatory hurdles
Requirements: Major pharmaceutical company planning international expansion requires additional regulatory resource for 2010. To join a 30-strong team based in the UK to support international regulatory affairs.