aris g jobs
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In depth knowledge and comprehension of safety databases, preferably Aris-g, including database structures... Systems Manager, Central London, Pharmacovigilance,Safety databases, Aris-g, Manager, Man Manager PV
Requirements: This role is responsible for the overall management and oversight of functioning, operating and output of the safety database for the Pharmacovigilance department.
Berkshire, Buckinghamshire, Hertfordshire, London, Oxfordshire, Surrey, Middlesex
Salary: Negotiable
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
Experience: N/A
Contract: any
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 research industry, offering
Requirements: * Science degree or nursing/pharmacist background * Minimum of 8 months experience in drug safety If this is of interest to you, or anyone you know, then contact Peter on 01189 594 990 or peter@clinicalprofessionals.co.uk
Director / PVG Head of / European Safety Reporting / London / ARIS G / SAE Reporting / Pharmacovigilance reporting / Senior Drug Safety Officer / Training / Trainer / PV Training / compliance / Compliance / Training and Compliance
Requirements: The primary purpose of this position is to develop, implement and manage Global PV specific QMS (Quality Management System) and compliance activities. You’ll also provide Pharmacovigilance (PV) expertise and assistance to support the overall QMS and manag
Berkshire, Buckinghamshire, Essex, London, Middlesex
Salary: Negotiable (33750 - 42750 £)
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
Experience: N/A
Contract: any
required timelines. - Maintain and update the global Safety Database (Aris G) - Pharmacovigilance... pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP
Contract: Any
required timelines. - Maintain and update the global Safety Database (Aris G) - Pharmacovigilance... pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP
Requirements: Drug Safety Manager/ Director Location: Switzerland This senior Drug Safety post will offer a varied and diverse role which will simulate and challenge those with previous Drug Safety management experience. Depending on the level of experience the success
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
Contract: Permanent
Any Location
Salary: Negotiable
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
Experience: 1 years
Contract: any
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 auditor consultancy consultant
Contract: Contract