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Role Title: Pharmacovigilance Scientist Duration: 12 Months Location: London Rate: £59 per hour - Umbrella (7.5 hour days) Role purpose / summary We are seeking a Pharmacovigil...
SRG are currently looking for a Regulatory Information Analyst for a Global Pharmaceutical Company who have opened a new vacancy within their team on an initial 12 Month basis to be b...
Regulatory submissionsRegulatory information management 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/NDARtQsJob Title: Report Writer Industry: Scientific 12 Month Contract £15 to £16 per hour Work From Home A...
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...
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 ModulesRole: Senior Programmer II Day Rate: Up to 520 OUTSIDE IR35 Skills: Oncology therapy area experience - Immuno-oncology experience would be a significant advantage Start Date: ASAP The Senior Pro...
CK Group are recruiting for a Senior Safety Physician to join a company in the Pharmaceutical industry at their site based in Cambridge on a contract basis for 6 months. Company: Our client is a glob...
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...
*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 documentsAt AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. Patient Safety at AstraZeneca ...
Site Name: UK - London - Brentford Posted Date: Jul 23 2020 Safety Scientist (Evaluation & Risk Management) GSK House – Brentford We are seeking a highly motivated individual to jo...
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...
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 Competitive Salary & Benefits At AstraZeneca when we see an opportunity for change we seize it and make it happen, because an opportunity no matter how small can be...
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