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aris g director
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
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
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
Contract: Permanent
Cardiff West Midlands
Company: Intapeople (T)Salary: £250 to £290 per year
: Recognised Oracle Qualifications (OCA/OCP), Oracle BPA Suite (ARIS), Oracle Web Services Manager, Oracle Service Registry, SQL and PL/SQL, Toplink, WSDL, WSIF, Oracle Middleware Components, (BI Suite, BAM, IDM Suite, Enterprise 2.0
Contract: contract
. Knowledge of medical and drug terminology.Knowledge of GCP and awareness of drug development process and importance of Safety. Good word processing computer skills;knowledge of a Safety DB (ARIS-g is an asset) PERSONAL SKILLS
Requirements: Drug Safety, Arisg
Contract: Contract 1 year
United Kingdom
Company: Oakleaf PartnershipSalary: £60000 - £70000 per annum + Extensive Benefits
including: * ARIS process maps * All letters, templates, e forms, paper forms, and documents associated with specific Reward and Benefit processes * Work with Portal team and Service Provider to ensure that up to date versions
Contract: Permanent
Any Location
Salary: Negotiable (35000 - 45000 £)
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: Permanent
Jobs similar to "aris": aris g director
Bedfordshire, Berkshire, Buckinghamshire, Cambridgeshire, East Sussex, Essex, Hertfordshire, London, Oxfordshire, Surrey, Middlesex
Salary: Negotiable (Up to 50000 £)
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
Experience: N/A
Contract: any
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: -Life Science degree -Experience within a drug safety department in clinical research If this opportunity is of interest to you or someone you know please contact Peter Speight on 01189 594 990 or peter@clinicalprofessionals.co.uk
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
Requirements: * Graduate with life science or healthcare degree and proven relevant industry experience within pharmacovigilance. * Understanding of the importance of pharmacovigilance in ethical pharmaceutical marketing and development. * Use of MS Office products to