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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
Requirements: * A life science degree or Medical degree * Proven experience within in Pharmacovigilance * Proven management experience * Written many PSURs from scratch
East Sussex
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
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
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
South East
Company: Clinical ProfessionalsSalary: £40K - £55K +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: * 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
Hertfordshire
Company: Clinical ProfessionalsSalary: Negotiable + Benefits
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 degree in biomedical science or Medical degree * 4-5 years of proven experience within in Pharmacovigilance * Proven management experience
, 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 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
Cambridgeshire
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
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
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
South East
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
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. * Understanding of the importance of pharmacovigilance in ethical pharmaceutical marketing and development. * Use of MS Office products to
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: * 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
/vendor handling ITIL (Must have) and project management (nice to have) certificates SLA management experience High comfort level and experience with virtual support teams Tools knowledge (ARIS, Solman, HP OVSD, HP QC) Experience
Other
Company: Careers SeekerSalary: £NEG Market rate
(e.g. Solution Manager, ARIS, etc) • Microsoft Office proficiency Business Experience: The job holder must be familiar with the project activities, organizational structure and the scope of the position for which services