Average salary: $92,900 /yearly
More stats ...sollicitées et de clarifications de données;
Assister et participer au processus de non-conformité/ACAP.
L’associé de la pharmacovigilance se verra également confier d'autres fonctions et tâches au besoin, de temps à autre.
Dans le cadre de ce poste, il peut être...
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...System (QMR).
Has a solid understanding of accounts payable and accounts receivable methodology.
In conjunction with the Pharmacovigilance Dept., assures collection, processing and reporting of Adverse Events within contractual KPI’s and pharmacovigilance requirements...
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...client site additions, from gathering information to tracking projects to completion
Draft and manage Quality Agreements and Pharmacovigilance agreements.
Oversee Appendix updates
Collect all necessary data from clients for new item releases
Ensure adherence to...
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...complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that...
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...Events to Health Canada, Med Info, and enter into source system and third-party systems
Report and document Adverse Events as per Pharmacovigilance requirements
Participate in quality activities and continuous improvement initiatives in keeping with the company's Quality...
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...for biostatistics, clinical operations, data management, statistical programming, CDISC, regulatory affairs, medical affairs and pharmacovigilance. ClinChoice has established major delivery centers across US, China, Europe, Canada, India, Japan and the Philippines. It has...
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...professionnel
~ Élaborer et mettre en œuvre les plans de perfectionnement individuel afin d'ameliorer le rendement au travail
Pharmacovigilance
~ Veiller à reperer et à declarer les manifestations indesirables et les plaintes relatives aux produits, conformement aux...
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...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
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...level of knowledge of ICH (International Conference on Harmonization), GCP (Good Clinical Practice) and Health Canada GVP (Good Pharmacovigilance Practices) guidelines appropriate to their hired role which is to be provided at time of hire and annually. With this knowledge...
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...and Regional Operations.
Collaborates internally with HQ functions, regional and local operations, EU Clinical Development, Pharmacovigilance, Global Medical Affairs to align on key issues/decisions across the trials. Consult with GHH as needed.
What you need to have...
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...Professional (e.g., Medical Doctor, Nurse, Pharmacist) or equivalent, with a minimum of 3-5 years’ experience in drug-safety or pharmacovigilance (preferred) and/ or experience in pharmaceutical industry.
• Bilingualism, English and French, both spoken and written.
• Knowledge...
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...listings for coded events to verify Medical Dictionary for Regulatory activities
Participate in bid defense meetings
Assist in Pharmacovigilance activities
Identify Program risks, and create and implement mitigation strategies with Clinical Operations
Ability to...
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...particulière, plainte ou contrefaçon (confirmée ou soupçonnée) concernant les produits de Lundbeck au Service Information médicale et Pharmacovigilance (****@*****.***) conformément à la formation qu’il (elle) aura reçue quant à la marche à suivre....
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...interests better
From early- to late-stage drug development, our range of services includes Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics,...
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...d’affaires des activités de son territoire
Soumettre régulièrement des rapports de dépenses.
Contacter le département de Pharmacovigilance lorsque l’on est au courant d’un effet indésirable associé à un produit de Pharmascience Inc., que l’information provienne d’un...
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...situations on our products as well as any product complaints or counterfeit or suspected counterfeit medicine to Medical Information and Pharmacovigilance (****@*****.***) as per training on current procedures.
Achievement of Sales objectives (50%)...
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...complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that...
Full time
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...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Full time
Contract work
Internship
Work visa
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
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...compliance.
~Assessing all complaints and Handling, Evaluating and Reporting of Adverse Drug Reactions complaints
~Manage Apollo’s Pharmacovigilance (PV) activities.
~Generate Annual Safety Reports for Apollo’s OTC products from Solicited and Unsolicited study, literature,...
Full time
Internship
Local area
Night shift
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Contract work
Internship
Immediate start
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Full time
Contract work
Work visa
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Contract work
Remote job
Internship
Immediate start
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Contract work
Internship
Flexible hours
2 days per week
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Contract work
Internship
Immediate start
Flexible hours
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
Holiday work
Contract work
Internship
Local area
Night shift
Weekend work
...better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical...
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Local area
...et les plaintes relatives aux produits, conformement aux normes de l'entreprise, dont la formation Responsabilites en matière de pharmacovigilance.
La personne ideale pour ce poste possède les qualifications suivantes :
Baccalaureat ès sciences ou baccalaureat en...
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3 days per week
...candidates are experts in key trial methodologies (e.g. study designs, patient engagement, trial ethics, data management and analysis, pharmacovigilance) and their appropriate areas of clinical trials research are connected to: biomarkers, drug safety and mechanism of action,...
Permanent employment
Carleton University
Ottawa, ON
13 days ago