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aris g director
South East
Company: Clinical ProfessionalsSalary: £42k - £48k + Benefits
pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO SUSARs SARs London West London Greater London South East England We
Requirements: * 3-5 years in pharmacovigilance, preferably in a CRO * Good understanding of the principles of Pharmacovigilance, including statutory requirements for pharmacovigilance data and working knowledge of Standard Operating Procedures relating to the transfer
Jobs similar to "aris": senior aris g, senior aris contract, senior aris knowledge, aris contract manager
South East
Company: Clinical ProfessionalsSalary: £33,750 - £42,750
drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO SUSARs SARs We are dedicated to the clinical
Requirements: * Life Science Degree * 3 years in pharmacovigilance, ideally in an oncology clinical trials setting. * Demonstrable experience in writing large Safety Reports
South East
Company: Clinical ProfessionalsSalary: £35k - £45k + Benefits
development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO
Requirements: * Life Science Degree * Over 5 years in Pharmacovigilance
health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO SUSARs SARs We
Requirements: * Life sciences degree or professional qualification eg, pharmacist, registered nurse * Preferably as leat one year's experience of Drug safety * Excellent understanding and working knowledge of medical terminology For more information or to apply for the
South East
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative
Requirements: * Relevant Medical qualifications (to include at least one higher medical qualification), significant and recent direct medical experience * Expertise in pharmacovigilance processes and associated medical issues (minimum 5 years) including PSURs, literatu
pharmaceutical biotechnology medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data
Requirements: * A life science degree or Medical degree * Proven experience within in Pharmacovigilance * Proven management experience * Written many PSURs from scratch
Hertfordshire
Company: Clinical ProfessionalsSalary: Negotiable + Benefits
health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO SUSARs SARs We
Requirements: * A degree in biomedical science or Medical degree * 4-5 years of proven experience within in Pharmacovigilance * Proven management experience
East Sussex
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
reports safety signal detection clinical pharmaceutical biotechnology medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg
Requirements: * A life science degree or higher * Excellent project management and organisational skills * Proven track record in Pharmacovigilance auditing For more information or to apply please email peter@clinicalprofessionals.co.uk or call 0118 959 4990
, medical research, drug safety, pharmacovigilance, adverse event reporting, aris g, Arisg, PSUR, adverse event, case processing, ADR, data physician, GMC, QP, narrative, Argus, SAE, reconciliation, safety, PV, DS, PVG, PVO, SUSARs
Requirements: - Life Science degree - Experience within a drug safety department in clinical research Preference - Argus experience - Virology and Oncology exposure - Locally based If this opportunity is of interest to you or someone you know please contact Peter Speig
South East
Company: Clinical ProfessionalsSalary: £40K - £55K +Benefits
detection clinical pharmaceutical biotechnology medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case
Requirements: * Previous safety database experience, Argus preferred. * Working knowledge of Structured Query Language (SQL). * Safety database maintenance experience including configuration, custom procedures and reporting. * Previous Pharmacovigilance experience
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