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Director, Pharmacovigilance Case Processing
UNITED KINGDOM, , UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Director, Pharmacovigilance (PV) Case Processing...
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
...day. Join us! What Medical Affairs does at Worldwide Medical Affairs impacts every stage in the lifecycle of a clinical investigation. From Business Development to Regulatory Submissions, members of the MA team support the larger project team and help establish the scientific and medical...
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Director, Pharmacovigilance Case Processing
UNITED KINGDOM, UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. /p p br /p p Director...
Medical Director – Medical Affairs & Clinical Dev
£200 +
LONDON
p strong Reference Number: JO-2307-518982 /strong br br Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below. br br Medical Director – Medical Affairs & Clinical Dev br br Rate: Negotiable br br Job Type: Permanent br...
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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...
Multilingual Medical Information Specialist - Norwegian Speaking
UNITED KINGDOM, , UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. The Multilingual Medical Information Specialist...
Pharmacovigilance Auditor
, , UNITED KINGDOM
...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
Pharmacovigilance Director of Projects (Europe, USA or Canada)
, , UNITED KINGDOM
We are PrimeVigilance (part of Ergomed PLC), a specialized mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information...
Medical Information Specialist - German Speaking
, , UNITED KINGDOM
Job Title: Medical Information Specialist - German Speaking Location : Remote (based in UK) Salary: Competitive Job Description Planet Pharma are currently partnered with a leading global Research Consulting Organization providing services to the Pharmaceutical, Medical Device and Biotechnology...
Quality Specialist
UNITED KINGDOM, , UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. The Opportunity The Quality Specialist position...
Technical Support Analyst
UNITED KINGDOM, , UNITED KINGDOM
...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. Our mission Our mission is to provide industry-defining implementations that are fast and intuitive to bring our customers an enjoyable and efficient experience. Widely regarded by our customers...
Senior Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...involve leveraging your medical expertise and extensive knowledge of pharmacovigilance (PV) legislation to contribute to our team. We are looking for an individual who excels in analytical thinking, can navigate complex data, establish structured processes, and effectively communicate information...
Senior Drug Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...Provide invaluable medical expertise to our Drug Safety and Pharmacovigilance team, supporting both medically trained and non-medical colleagues. Spearhead training and mentoring initiatives, empowering our team to excel in clinical safety data interpretation and risk management. Act as a...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, UNITED KINGDOM
...650 products covering medical devices, cosmetics and biocides, currently sold in 7 markets across Europe., with plans for further expansion. This role requires an individual who can be flexible, deliver at pace, deal with ambiguity and demonstrate a strong capability for developing productive...
Director, Drug Safety Lead
, , UNITED KINGDOM
...with high unmet medical need. Bicycle is headquartered in Cambridge, UK, and our US operations run out of Cambridge, MA. Culture is key and all Bicycle employees actively embrace and role model our company values: Weare Adventurous .We believe it s...
Quality & Technical Manager
, , UNITED KINGDOM
...and update SOPs Manage Medical Information Service provider & respond to MI enquiries where required. Preparation, management and review of technical agreements and safety data exchange (PV) agreements Liaise with Marketing Authorisation holders with respect to pharmacovigilance responsibilities...
Senior Manager, Quality
ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM
...with high unmet medical need. Bicycle is headquartered in Cambridge, UK, and our US operations run out of Cambridge, MA. Culture is key and all Bicycle employees actively embrace and role model our company values: Weare Adventurous .We believe it...
Regulatory Clinical Trials Submission Manager
UNITED KINGDOM, , UNITED KINGDOM
ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions...
Complaints Intake Analyst
, , UNITED KINGDOM
...like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance Supports more complex complaints that are escalated Serve as a Subject Matter Expert for a designated product(s) within the team when required Where applicable, decide whether a replacement, credit, or warranty...
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