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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
Jobs similar to "aris": aris g director
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
and provide scalable platforms; * Experience of working with enterprise architecture tools e.g. Alfabet, Rational Rose, IGrafx, Mega, Aris; * Experience or an understanding of the key architectural methodologies such as TOGAF, Zachman
Contract: Permanent
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: * Graduate with life science or healthcare degree and proven relevant industry experience within Pharmacovigilance. (Minimum of 6 Months experience). * Understanding of the importance of Pharmacovigilance in ethical pharmaceutical marketing and developmen
, 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: * 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
South East
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
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
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
Cambridgeshire
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
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
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
, 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
Jobs similar to "aris": aris administrator manager
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