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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
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
, 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: £42k - £48k + 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: * 3-5 years in pharmacovigilance, preferably in a CRO * Good understanding of the principles of Pharmacovigilance, including statutory requirements for pharmacovigilance data and working knowledge of Standard Operating Procedures relating to the transfer
Jobs similar to "aris": senior aris contract manager, senior aris uk
South East
Company: Clinical ProfessionalsSalary: £33,750 - £42,750
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: * Life Science Degree * 3 years in pharmacovigilance, ideally in an oncology clinical trials setting. * Demonstrable experience in writing large Safety Reports
South East
Company: Clinical ProfessionalsSalary: £35k - £45k + Benefits
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
Requirements: * Life Science Degree * Over 5 years in Pharmacovigilance
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: * 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
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
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
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
Requirements: * Life sciences degree or professional qualification eg, pharmacist, registered nurse * Preferably as leat one year's experience of Drug safety * Excellent understanding and working knowledge of medical terminology For more information or to apply for the
South East
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
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 GMC We are dedicated to the clinical research industry
Requirements: * Relevant Medical qualifications (to include at least one higher medical qualification), significant and recent direct medical experience * Expertise in pharmacovigilance processes and associated medical issues (minimum 5 years) including PSURs, literatu