aris g jobs
1-10 of 105 jobs "g"Central London
Company: AXESSSalary: On Application
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.
Bedfordshire, Berkshire, Buckinghamshire, Cambridgeshire, Essex, London, Middlesex
Salary: Negotiable
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
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
Berkshire, Buckinghamshire, London, Oxfordshire, Surrey
Salary: Negotiable
, 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
Experience: N/A
Contract: Permanent
update 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 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 candidates a unique service
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 Argus SAE
Requirements: •Graduate with life science or healthcare degree and proven relevant industry experience within Pharmacovigilance. •Experience of working with a global safety database, MedDRA coding and E2B reporting •Review of scientific documents •Understanding of the
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: Drug Safety Scientist Our client are a leading company specialising in pharmaceutical research and development. They are looking to expand their Drug Safety team and are looking for a Drug Safety Scientist on a 6 month temporary contract.
Any Location
Salary: Negotiable
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 PSUR adverse
Experience: N/A
Contract: any
/ Safety / Drug Safety / PV Line Manager / PVG Associate Director / PV Senior Manager Drug Safety Scientist / PVG Associate Director / PVG Head of / European Safety Reporting / London / ARIS G / SAE Reporting / Pharmacovigilance
Requirements: Excellent opportunity to join a recently reoganised and centralized Global PV team as the Compliance and Training expert. This is a permanent position based from the Global Headquarters in Middlesex.
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
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