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SciPro have exclusively partnered with an innovative pharmaceutical company who are driven by their purpose to reimagine how drugs can improve the quality of life of patients with rare disease. They a...
PE Global is currently recruiting for a Medical Writer for a leading multi-national pharmaceutical client based in London. The client is offering the option to work remotely.
*Contract Medical Writer - 12 month contract - Pharmaceutical - London - OUTSIDE IR35* My client a top Pharmaceutical has a need for a Medical Writer to join their team on an initial 12 month contra...
Medical WritingPharmaceuticaleditingreviewingwritingCSRprotocolsINDsCONTRACTclinical study reportsCTDsClinical WritingOUTSIDE IR35BLA/NDARtQsCK Group are recruiting for a Senior Regulatory Affairs Associate to join Health and Wellness company based in Warwickshire with flexible home working available. This position will work on projects an...
Job: Medical Safety Writer Pharmacovigilance Salary: up to £70,000 Location: Fully remote from anywhere in the UK Blue Pelican Reference: 28223 Working in drug saf...
Senior Regulatory Affairs, contract job, Emerging Markets, virology, Asia, LATAM, Africa, Middle East, EEU Senior Regulatory Affairs Associate - Emerging Markets Your new company Th...
Are you an experienced Medical Writer or Pharmacovigilance Specialist looking for an exciting new job opportunity We are currently looking for a Medical Writer Principal - Pharmacovigilance to join a...
Are you an experienced PVG Database Principal looking for an exciting new job opportunity We are currently looking for a PVG Database Principal to join a leading pharmaceutical company based in the W...
Company Description Mundipharma is a global (ex-US) network of independent associated companies that research, develop and manufacture innovative pharmaceutical medicines and consume...
*Senior Pharmacovigilance Scientist - Aggregate reports, signal & Risk management -Top Pharma - 12m contract* My client is a Global Biopharmaceutical company and they have a position available for a...
PharmacovigilanceRisk ManagementPSURscontracthomebasedhybridDSURssignal detectionsignal managementAggregate reportsRMPsPBRERsPADERssignalevaluation*Contract Medical Writer - 12 month contract - Pharmaceutical - London - OUTSIDE IR35* My client a top Pharmaceutical has a need for a Medical Writer to join their team on an initial 12 month contra...
PharmaceuticalProtocolscontracthomebasedMedical WriterManuscriptsClinical Study ReportsSafety ReportsSubject Narrativesclinical/regulatory documentsInvestigator BrochuresRegulatory Submission ModulesWe have an exciting opportunity for a Senior Specialist, Regulatory Affairs to join a thriving pharmaceutical organisation based in Shoreditch, London. This is a full-time temporary contract role init...
PharmaceuticalRegulatory AffairsAuthorisationsMHRATracking SystemsThe Role The Regulatory Affairs team is responsible for legal compliance of all Holland & Barrett Internationals Foods & Food Supplements, Cosmetics and Licenced Products (including ...
CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the Pharmaceutical industry at their site based in Cambridge on a contract basis for 6 or 12 months. Company: Our...
*Senior Pharmacovigilance Safety Scientist - Global BioPharma - 12-month contract - OUTSIDE - UK REMOTE* My client is a Global Biopharmaceutical company and they have a position available for a Seni...
Pharmaceutical Pharmacovigilance PV Risk Management Plans PSURs contract Pharma DSURs signal detection outside of IR35 RMPs aggregate safety repts PBRERs PADERs management and evaluation Remote within UKSenior PV Scientist Cambridgeshire Brief Senior PV Scientist needed for a multinational Pharmaceutical organisation based in Cambridgeshire who are looking to employ an experienced and well-rounded...
Drug Safety Scientist Safety Evaluation and Risk Management Global Pharmaceutical company Harrow The SERM Scientist will sit within the Global Drug Safety team and will take responsibility for all sa...
Role: - Regulatory Affairs Associate Salary: - Competitive Location: - Manchester Russell-Taylor Group have a fantastic opportunity for a regulatory affairs associate/officer to join a rapidly expa...
*Senior Pharmacovigilance Safety Scientist - Global BioPharma - 6-month contract* My client is a Global Biopharmaceutical company and they have a position available for a Senior Pharmacovigilance Sa...
Pharmacovigilance Risk Management PV PSURs REMS DSURs signal detection Aggregate repts RMPs signal management process protocol review ICF review* Pharmacovigilance Medical Writer - Global Pharma - 3-month contract - UK, Remote* My client is a Global Pharmaceutical company and they have a position available for a Pharmacovigilance Medical Wr...
GCP Pharmaceutical Pharmacovigilance Protocols RMP PV PSUR Medical writing DSUR Clinical Study Repts Regulaty documents Subject Narratives clinical writing Investigat Brochures Regulaty Submission Modules Safety documentsRole: - Junior Regulatory Affairs Salary: - Competitive Location: - Manchester Russell-Taylor Group have a fantastic opportunity for a junior regulatory affairs associate/officer to join a rapidly ...
Working at Johnson & Johnson can change everything. Including YOU. By joining a company that has been carving out the future of healthcare for more than 130 years, you will be offered a career...
Site Name: UK - London - Brentford, UK - Middlesex - Stockley Park Posted Date: Jul 30 2020 Are you a safety/pharmacovigilance physician with in-depth and hands-on experience Do you want to work on th...
Location: Cambridge Competitive Salary & Benefits At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost...
CK Clinical are recruiting for a Regulatory Affairs Executive to join a niche organisation that focuses on respiratory and rare diseases based at their offices in Manchester on a permeant basis Regul...
Site Name: UK - London - Brentford Posted Date: Jun 9 2020 An exciting opportunity has arisen for a Manager, CH Safety Evaluation and Risk Management to join GSK’s Consumer Healthcare Safety Evalua...
Senior PV Medical Writer Global Pharmaceutical Company Hertfordshire Competitive Salary + car allowance + bonus Are you an experienced PV Specialist/Manager with experience of writing aggrega...
*PV Medical Writer - 12 month contract - Pharma - London* My client a top Pharmaceutical has a need for a Pharmacovigilance Medical Writer to join their team on an initial 12 month contract. Within...
Pharmaceutical PSURs editing reviewing writing protocols Medical writing INDs DSURs clinical study repts Regulaty submissions BLA/NDAs CTDs Clinical studies .Location: Cambridge, England, United Kingdom Global Medicine Development drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ...
PE Global are currently recruiting for two Medical Writers for a 12 month contract role with a leading multi-national Biotech client based in London. The role The Contract Medical Writer applies int...
*Senior Pharmacovigilance Safety Scientist - Global BioPharma - 12-month contract* My client is a Global Biopharmaceutical company and they have a position available for a Senior Pharmacovigilance S...
Pharmacovigilance RMP PSUR Seni contract Berkshire authing DSUR signal detection aggregate repts© 2019 Naukrijobs All Rights Reserved