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Job matches 40

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Senior Regulatory Affairs Manager - West London Contract

Company: Key People Limited
Location: West London
Salary: 100,000+
Closing Date: 24 Aug 17More Details
Within this role you will provide regional regulatory support for one or more products, and as a member of the Global Regulatory Team (GRT), will be accountable for developing and executing regional regulatory strategies across the product lifecycle and managing effective agency interactions.

Senior Regulatory Consultant - 12 month contract

Company: Key People Limited
Location: Uxbridge
Salary: Negotiable
Closing Date: 23 Aug 17More Details
Within this role you will provide regional regulatory support for one or more products, and as a member of the Global Regulatory Team (GRT), will be accountable for developing and executing regional regulatory strategies across the product lifecycle and managing effective agency interactions.

Regulatory Publishing Specialist - London

Company: Key People Limited
Location: West London
Salary: 40,000 - 60,000
Closing Date: 24 Aug 17More Details
A well established pharmaceutical company based in South West London is currently recruiting for an experienced publisher to join their growing team. Within this role you will be responsible for all eCTD submissions and will have the chance to gain technical regulatory experience, if desired.

Senior Scientist or Principal Scientist

Company: Key People Limited
Location: Basel
Salary: 100,000+
Closing Date: 23 Aug 17More Details
Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures with members of the own and crossfunctional teams. Manage technical lab activities.

International Copy Approval Associate

Company: Key People Limited
Location: Marlow
Salary: Negotiable
Closing Date: 15 Sep 17More Details
Participate as a Core Team Member of the International Brand TeamsProviding clear and constructive advice and guidance on advertising and promotional compliance to the Business Unit/function. Undertake approval of international promotional materials and activities in accordance with the company's international approval processes and SOPs as well as all applicable relevant regulations and legislation.Lead projects

Global Safety Manager

Company: Key People Limited
Location: Cambridge
Salary: Negotiable
Closing Date: 30 Aug 17More Details
This is an excellent opportunity for a pharmacovigilance professional to join an established company as a Pharmacovigilance Manager.Your main accountabilities will be to manage the development, implements, and monitor profitability, objectives, metrics of assigned group of direct reports.Identifies and implements improvements of drug safety center processes through review of projectWriting and reviewing of Risk Management plans, PSUR's and DSUR's. ...

Senior Regulatory CTA Submissions Manager

Company: Key People Limited
Location: Buckinghamshire
Salary: 60,000 - 80,000
Closing Date: 24 Aug 17More Details
A leading pharmaceutical company currently seeks a Senior Regulatory Consultant to join their team on an initial 6 month contract basis. Within this role you will be responsible for managing regulatory Clinical Trial Applications (CTA) submission activities (Phase 1 - 4 spanning five therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease).

Senior Regulatory Affairs Officer - West London!

Company: Key People Limited
Location: West London
Salary: 30,000 - 40,000
Benefits: bonus and excellent benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for a Senior Regulatory Officer to join a Pharmaceutical company based in West London - hands on eCTD submission experience is essential.Within this role you will be responsible for registering an exciting range of new products and maintaining a European Portfolio. Working in a small team, you will be exposed a vast range of responsibilities and gain a huge amount of experience within a short amount of time!

Senior Regulatory Officer, Regional Labeling

Company: Key People Limited
Location: Hertfordshire
Salary: 30,000 - 40,000
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for an experienced and driven candidate to join the labelling team within a global healthcare company based in Hertfordshire. You will be responsible for authoring and maintaining SmPCs and PILs, as well as responding to questions from authorities and supporting central regulatory teams.

Senior Regulatory Officer, EU

Company: Key People Limited
Location: Hertfordshire
Salary: 40,000 - 60,000
Benefits: bonus + excellent benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen to join a leading Generics company at Senior Regulatory Officer level with the potential to gain line management responsibilities. Within this role you will provide technical advice and oversee projects for new and existing European and International licences.

Director / Head of Regulatory Affairs

Company: Key People Limited
Location: Hertfordshire
Salary: 60,000 - 80,000
Benefits: car, bonus, benefits
Closing Date: 24 Aug 17More Details
A rare opportunity has arisen for a Regulatory Affairs Director / Head of Regulatory to lead the UK & Ireland Affiliate team based within a Top 5 Generics company based in Hertfordshire. Within this role you will lead a team of four people, two Senior Officers and two Principle Officers, and oversee the integration of two teams.

Pharmacovigilance Officer (SDEA experience required)

Company: Key People Limited
Location: Richmond upon Thames
Salary: Negotiable
Closing Date: 15 Sep 17More Details
Your responsibilities will include;Working with SDEA’sGlobal and Local literature searching, handling medical enquiries and responding to them by phone and emailUnderstanding SMPC’s, reconciliation and working closely with the QP. They are really looking for candidates who are interested in RMPs, PSUR activity and you would be involved in both Regs and PV.

Regulatory Affairs Manager

Company: Key People Limited
Location: Hertfordshire
Salary: 40,000 - 60,000
Benefits: bonus and benefits
Closing Date: 24 Aug 17More Details
Reporting into the Head of Regulatory Affairs, within this role you will be responsible for the registration of new products and the maintenance of existing products.

International Clinical Project Manager, Phase II/III

Company: Key People Limited
Location: Switzerland
Salary: 100,000+
Closing Date: 31 Aug 17More Details
Our leading pharmaceutical client is looking for an International Clinical Project Manager to focus on large phase II/III trials.The successful applicant will be required to provide the operational expertise and leadership to clinical operations teams to ensure the effective and efficient delivery of all operational aspects of clinical studies (Plan, Initiate, Conduct, Close), in accordance with ICH/GCP. ...

Clinical Research Study Leader – Phase I/II

Company: Key People Limited
Location: Switzerland
Salary: 100,000+
Closing Date: 31 Aug 17More Details
Our client is looking for proven clinical project management professionals with leadership experience to manage early phase clinical trials - First in Man through to Proof of Concept studies.The role of the Study Leader is to provide leadership for one or more global projects including responsibilities for delivering internally managed as well as outsourced studies. ...

Global Clinical Project Manager, Phase IV

Company: Key People Limited
Location: Switzerland
Salary: 100,000+
Closing Date: 31 Aug 17More Details
Our leading pharmaceutical company is looking for a Global Clinical Operations Project Manager to focus on the clinical operations duties of medical affairs projects.The position has a pivotal role in implementing and supervising the execution of clinical trials programs and will be responsible for managing all activities related to clinical trials with Pharma Development, Clinical Research Organisations and the Affiliate companies.

Associate Director, Promotional Regulatory Affairs

Company: Key People Limited
Location: Oxfordshire
Salary: 60,000 - 80,000
Benefits: bonus, car allowance and share scheme
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for an Associate Director, Promotional Regulatory Affairs, EU/ROW to join a growing Biopharma based in Oxfordshire. Within this role you will serve as an internal expert on European (EFPIA) and International (ex-US) regulations governing the promotion of prescription pharmaceutical products.

Associate Director, Regulatory Affairs - Hertfordshire

Company: Key People Limited
Location: Hertfordshire
Salary: 60,000 - 80,000
Benefits: car allowance, bonus and usual benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for an Associate Director, Regulatory Affairs to join a global pharmaceutical company based in Hertfordshire. Within this role you will oversee the submission of global submissions, ranging from CTAs through to registrations and post approval.

Principle Regulatory Affairs Officer - Hertfordshire

Company: Key People Limited
Location: Hertfordshire
Salary: 40,000 - 60,000
Benefits: bonus + excellent benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen to join a leading Generics company at a Principle Regulatory Officer level with line management responsibilities. Within this role you will be responsible for managing a team of 4 - 6 regulatory professionals and provide technical advice and oversee projects for new and existing European and International licences.

Regulatory Affairs Manager - EU submissions

Company: Key People Limited
Location: Essex
Salary: 40,000 - 60,000
Benefits: bonus and benefits
Closing Date: 24 Aug 17More Details
My client, a top 15 pharmaceutical company based in Essex is currently searching for a Regulatory Affairs Manager to join their team and oversee a regulatory officer. If you have a strong background in European Regulatory Affairs and enjoy working in a varied and fast-paced environment, this role could be a great fit for you.

Regulatory Affairs Officer - EU Submissions

Company: Key People Limited
Location: East London
Salary: 30,000 - 40,000
Benefits: benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for an experienced Regulatory Affairs Officer to join the EU team at one of the largest pharmaceutical companies in the world. Within this role you will be responsible for registrations and life cycle maintenance across Europe and will have the opportunity to progress your career and take on more responsibility as your experience grows.

Senior Data Manager / Data Manager - FRANCE

Company: Key People Limited
Location: Paris
Salary: 30,000 - 40,000
Closing Date: 24 Aug 17More Details
Our client, a Paris based Pharmaceutical company, currently seek an experienced Data Manager to join their team on a permanent basis due to a period of growth. The ideal person will have a STRONG background in using CLINSIGHT software.

Regulatory / Medical Writer - Paris

Company: Key People Limited
Location: Paris
Salary: 40,000 - 60,000
Benefits: bonus and benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for an experienced Regulatory Writer / Medical Writer to join a leading pharmaceutical company specialising in the discovery, development, and commercialisation of novel targeted therapies for treating cancer, chronic inflammatory diseases and neurological degenerative disorders.

Senior Director - Project Management

Company: Key People Limited
Location: Zürich
Salary: 100,000+
Closing Date: 21 Aug 17More Details
Key People are looking for a Senior Director Project Management to work for our pharmaceutical client based in Switzerland.

Senior Statistical Programmer

Company: Key People Limited
Location: London
Salary: 60,000 - 80,000
Closing Date: 24 Aug 17More Details
My client is seeking an experienced SAS Programmer to join a leading Pharmaceutical company on an initial 12 month contract basis based in West London.

Regulatory Affairs Officer

Company: Key People Limited
Location: East Midlands
Salary: 30,000 - 40,000
Benefits: bonus and benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for a Regulatory Officer with 1-3 years of experience to join a leading Pharmaceutical company based in East Anglia.

Regulatory Affairs Manager, Sussex

Company: Key People Limited
Location: East Sussex
Salary: 40,000 - 60,000
Benefits: bonus and benefits
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for a Regulatory Manager / Team Leader to join a global team within a specialist Pharmaceutical company based on the south coast. Within this role you will gain a large amount of exposure working closely with R&D, QA and PV teams and lead a team of Regulatory professionals.

Head of Drug Safety-Physician

Company: Key People Limited
Location: Paris
Salary: Negotiable
Closing Date: 15 Sep 17More Details
Your main responsibilities will include the following; Medical review of serious adverse events and non-serious adverse events from spontaneous reports and reports derived from regulatory authorities and the medical literature during postmarketing surveillance. ...

Clinical Trial Pharmacist

Company: Key People Limited
Location: Uxbridge
Salary: Negotiable
Closing Date: 30 Aug 17More Details
The Clinical Research Pharmacy Services team is a highly talented group of Pharmacists dedicated to oversight of Investigational Product in the companies Studies. This team has an intimate understanding and insight into trial site practice, provides investigational product clinical services and relays how Investigational Product should be handled and managed within clinical sites. The team drives and contributes to continuous process improvement relating to Investigational Product.

Senior Biostatistician - Paris based

Company: Key People Limited
Location: Paris
Salary: 30,000 - 40,000
Closing Date: 24 Aug 17More Details
An excellent opportunity has arisen for a Senior Statistician to join a leading Pharmaceutical company based in Paris. This role has become available due to a period of growth within the company and will offer exposure to extensive clinical development exposure within oncology and in inflammatory and neurodegenerative diseases.
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