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Qualified Person, Pharmacovigilance (QPPV)
LUTON, ENGLAND, UNITED KINGDOM
My client specialises in the licensing and marketing cost-effective generic pharmaceuticals and is focused on growth through product launches and EU expansion. They want to increase their commercial foothold in the EU and expand their UK PV team. They are looking for a QPPV to ensure constant...
Senior Pharmacovigilance Manager
41680
WEYBRIDGE, SURREY, WEYBRIDGE, SURREY
Hobson Prior is seeking a Senior Pharmacovigilance Manager. The successful candidate will maintain the overall safety profiles and any emerging safety concerns concerning the pharmaceutical products. This role is crucial in managing all pharmacovigilance risk management issues and acting as the UK...
Senior Medical Director - CNS/Neurology - Europe - Home-based
LONDON, ENGLAND, UNITED KINGDOM
...course of the trial. Pharmacovigilance activity for adverse event analyses and reporting and a medical writing group are integral part of the service offering. Medical Affairs also partner with other functional groups within the Worldwide organization, the generation of statistical and clinical...
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Qualified Person, Pharmacovigilance (QPPV)
UNITED KINGDOM, UNITED KINGDOM
p My client specialises in the licensing and marketing cost-effective generic pharmaceuticals and is focused on growth through product launches and EU expansion. They want to increase their commercial foothold in the EU and expand their UK PV team. /p p br /p p They are looking for a QPPV to...
Manager, Global Aggregate Reports quality and compliance
BERKSHIRE, ENGLAND, UNITED KINGDOM
...of new and evolving pharmacovigilance legislation within the GRIP process. Coordinates the Aggregate Reports Quality Review Board and overseeing Aggregate report KPIs across CSL business units. The authoring of high quality regulatory required aggregate reports including scientific analysis...
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Head of Global Safety Data Integration and Literature (UK)
£80 - 100
SLOUGH
...team in the Product Pharmacovigilance & Device Safety team, ideally based in our Raleigh (US), Monheim (Germany), Slough (UK) or Brussels (Belgium) offices. /p p b About the role: /b /p p You will play a pivotal role in oversight and implementation of new and improved solutions to...
Quality & Technical Manager
, , UNITED KINGDOM
...agreements Liaise with Marketing Authorisation holders with respect to pharmacovigilance responsibilities. Report Medical Information and PV data to MA holders Undertake RPi duties for the Company & deputy Consultant RPi as required. Routine Supplier audits with consultant QP/RPi Conduct annual...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, UNITED KINGDOM
...Regulatory Affairs and Pharmacovigilance in specific projects related to Alvita, including assessing the launch in new territories or the development of new processes necessary to deliver compliance with European and local legislation. You will support the European Head of Pharmacovigilance and...
Regulatory Affairs Role
HAMPSHIRE, ENGLAND, UNITED KINGDOM
...applications to obtain marketing authorisations Voicing affiliate perspective and needs to global and regional regulatory contacts Ensuring timely responses to requests from support groups and/or regulatory authorities Maintaining marketing authorisations (timely submission of post-approval...
Regulatory Affairs Associate
, , UNITED KINGDOM
...UK, Ireland and Maltese marketing affiliates. Responsibilities: Implement Regulatory Plan in-line with affiliate business plans Ensure Submissions and Approvals for Regulatory Applications in a timely manor. Prepare and support new MAAs Assist with the maintenance for MAAs Interact with Health...
Decontamination Service Supervisor
, , UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
MSL - small Pharma
, , UNITED KINGDOM
...previously Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory...
Key Account & Access Manager - Diabetes
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
...Implementation of marketing strategies: Area Management : Effective management of the territory through the optimal selection of activities for the management of healthcare institutions, doctors, pharmacists, and medical staff considering the knowledge of the decision-making areas visited...
Strategy Consultant
, , UNITED KINGDOM
...from philosophy to pharmacovigilance. Proactive & Self-Starter: You crave independence and the ability to pioneer new ideas of your own. You naturally assume responsibility, work under your own initiative, are resourceful and have that entrepreneurial spirit to get started now . Adventurous...
Medical Territory Account Manager
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
...including complaint and pharmacovigilance reporting Your Background Degree qualified in life science or equivalent Experience of working in a relevant hospital sales role and full UK driving license ABPI qualified understands the ABPI code of conduct and applies it accordingly A nursing...
Senior Director, Global Patient Safety - Ophthalmology
61651
UXBRIDGE, LONDON (GREATER), UXBRIDGE, LONDON (GREATER)
...regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required. Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest. Familiarity...
Senior CRA - Sponsor dedicated - Rare Disease - United Kingdom (homebased) - National travel across
38195
; HOMEWORKING, , UNITED KINGDOM; HOMEWORKING,
...violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): o Assesses site processes o Conducts Source Document Review of appropriate site source documents and medical records o Verifies required clinical data entered in the case report form...
Adverse Event Intake Specialist with English and Turkish language
36662
ISTANBUL, , ISTANBUL,
...To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming. Adverse Events(AE)/endpoint information. Determining initial/update status of incoming events. Database entry. Coding AE and Products, writing narratives...
National Sales Manager - Women's Health
LONDON, ENGLAND, UNITED KINGDOM
...compliance with Pharmacovigilance, CRM systems, expenses systems, and PM systems. Develop and nurture customer relationships to enhance therapy area knowledge and brand loyalty. Identify and create partnership opportunities with customers and patients to drive growth and market share...
Engagement Manager - R&D (Remote)
LONDON, ENGLAND, UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You'll Do Lead multiple project engagement teams empowering the team to plan and manage all aspects of delivery, from scope to quality assurance Be responsible for the end-to-end design, build, and delivery of...
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