Salaire moyen: $88 222 /annuel
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$65k - $70k par année
...pharmaceutical company with a focus on meeting the needs of patients, physicians and partners. We are located in Oakville, Ontario. Pharmacovigilance and Medical Information Associate Job Description & Key responsibilities The Pharmacovigilance Associate will provide...SuggéréTravail au bureau$30 - $48 par heure
...recognized training and current competencies have been demonstrated and updated per standards. Maintain role related, medication and pharmacovigilance training as required. Observe and document patient conditions. Report and document Adverse Events as per Pharmacovigilance...SuggéréTaux horaireTemps partielRecrutement immédiat$99.2k - $124k par année
...submission, dossier compilation) Act as the Canadian regulatory lead on global and local project teams Ensure compliance to the Pharmacovigilance requirements by reporting any safety information to Teva Pharmacovigilance team as per required training Communicate...SuggéréStageTravail au bureauZone localeLe monde entier$57k - $71k par année
...Responsibility (Only Applicable To Customer Facing Roles) Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day Qualifications An effective team player with proven...SuggéréStageTravail au bureauTravail posté$55k - $65k par année
...experience) ________________________________________________________________________________ POSITION SUMMARY: The Pharmacovigilance (PV) and Quality Associate is responsible for supporting and maintaining all pharmacovigilance and quality assurance activities...SuggéréEmploi permanentTemps pleinTravail au bureauLundi au vendredi- ...Responsibility (Only Applicable To Customer Facing Roles) Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day Qualifications Enrolled in or recently graduated...SuggéréStageTravail au bureau
- ...coordinating responses to centre queries and Research Ethics Board (REB) provisos, in consultation with CCTG Study Coordinators and the Pharmacovigilance Team. • Works collaboratively with trial teams and the ETL in determining whether centre consent forms adequately include...SuggéréTravail au bureau
- ...We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services...SuggéréTemps pleinLe monde entier
- ...Health Canada and enter into source system and third-party systems, as applicable Report and document adverse events as per pharmacovigilance requirements. Participate in ongoing internal and/or external continuing education activities. Adhere to Bayshore Policies...SuggéréСontratEmploi en cddRecrutement immédiatTravail à distanceBureau à domicile
- ...Direct the design, protocol development, analysis plan, execution, interpretation, and reporting of PASS, PMCs/PMRs, and other pharmacovigilance studies using EHR/claims and other real-world data sources. Advance regulatory science : Develop, justify, and defend epidemiological...SuggéréContrat Longue DuréeEmploi permanentСontratTravail temporaireEmploi en cddTravail au bureauRecrutement immédiat3 jours par semaine
- ...decision is received, ideally securing coverage for the patient. Report and document Adverse Events as per training on updated Pharmacovigilance requirements. Adhere to Sentrex Policies and Procedures. Additional duties as determined by your Manager. What you need...SuggéréTaux horaireEmploi permanentTemps pleinTravail à distanceLundi au vendrediHoraires flexibles
- ...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...SuggéréTemps pleinRecrutement immédiatTravail à distance
- ...SOPs, ICH GCP and country regulations. This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central...SuggéréСontratRecrutement immédiat
- ...appraisals of published safety studies related to medicinal products and devices; communicate findings with clear implications for pharmacovigilance and risk management. Essential Skills/Experience PhD (or equivalent) in epidemiology, public health, or related health...SuggéréContrat Longue DuréeEmploi permanentСontratTravail temporaireEmploi en cddTravail au bureauZone localeRecrutement immédiat3 jours par semaine
- ...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes Conducts Source Document Review...SuggéréContrat En CoursСontratEmploi intérimZone localeRecrutement immédiatTravail à distance
- ...Responsibility (Only Applicable To Customer Facing Roles) Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day Qualifications Undergraduate students pursuing a major...StageTravail au bureau
$125.12k - $173.7k par année
...leveraging analytics to optimize performance and enhance the customer journey Ensure adherence to regulatory, compliance, and pharmacovigilance standards, including timely reporting of adverse events Support governance, SOP standardization, and operational discipline...Zone localeProgramme de réinstallationHoraires flexibles$67.05k - $89.4k par année
...for roles such as CRAs, Clinical Trial Managers, Clinical Scientists, Data Managers, Biostatisticians, Regulatory Affairs, and Pharmacovigilance professionals. Maintain strong candidate pipelines, track recruitment metrics in ATS/CRM systems, provide regular updates to...Temps pleinСontratTravail à distanceLundi au vendrediHoraires flexiblesKelly Services
CanadaIl y a un mois- ...Performance Digital Technology & Solutions Data Science Manufacturing Technology Marketing Occupational Health Pharmacovigilance Regulatory Affairs Scientific and Medical Affairs Site Quality Operations Supply Chain Management Technical...StageTravail au bureauTravail à domicileLe monde entier
- ...About the Role: We are seeking Patient Safety Specialists to join our team, working closely with our global pharmacovigilance teams across clinical trials and post-marketed projects. The successful candidate will contribute to the execution of safety processes with increasing...FreelanceZone locale
- ...(s) assigned to the trial Reviews protocol deviations Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues Reviews IND/SUSAR Safety Reports, updates/...Temps pleinСontratTravail à domicile
- ...You are: ~ Bachelor’s degree in health science. Commensurate experience will be considered. ~5+ years industry experience in pharmacovigilance, clinical research, and/or clinical data management required, and 4 years coding experience. ~ Expertise in medical...Travail à distanceEmploi permanent
- ...en assurer le suivi Participer et s’impliquer lors des réunions de ventes Assurer le respect des exigences en matière de pharmacovigilance en signalant les événements indésirables et d’autres données de sécurité à l’unité PV (pharmacovigilance) de Teva Respecter les...ApprentissageTravail au bureauRecrutement immédiatHoraires flexibles
$75k - $130k par année
...who is eager to drive product advancement and innovation. In this role, you will be guiding the development of a game changing pharmacovigilance (drug safety) product and continuing Veeva’s success as the leading provider in cloud-based technology for Life Sciences. What...Travail au bureauZone localeTravail à distanceTravail à domicile- ...healthcare or pharmaceutical industry. ~ Familiarity with pharmaceutical go-to-market strategies, IMC Code of Ethical Practices, and Pharmacovigilance standards. ~ Expertise in brand planning, including the ability to translate disease state and business drivers into patient...Contrat Longue DuréeEmploi permanentСontratTravail temporaireEmploi en cddTravail au bureauHoraires flexibles3 jours par semaine
- ...review of SAE form, and reviews SAE causality assigned by the Investigator. Write and/or review SAE narratives Work with the Pharmacovigilance Services provider or Marketing Authorization Holder (MAH) to review SAEs and follow-up on outstanding safety queries, interact...RemplacementEmploi permanentTemps pleinСontratTravail à distanceTravail à domicileHoraires flexiblesTravail posté
- ...Submissions (NDS) and Abbreviated New Drug Submissions (ANDS) in eCTD format. Clinical Review: Interpret clinical trial data and pharmacovigilance reports to support safety and efficacy claims in dossiers. Agency Interaction: Act as the liaison with Health Canada’s...Temps plein
- ...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP):Assesses site processes. Conducts Source Document Review...СontratEmploi intérimZone localeRecrutement immédiatTravail à distance
- ...Receive and track customer phone calls or emails Participate and get involved during sales meetings Ensure compliance to the Pharmacovigilance requirements by reporting any safety information to Teva Pharmacovigilance team as per required Maintain compliance in...Travail temporaireTravail au bureauLe monde entierHoraires flexibles
$146k - $277k par année
...contact for customers for assigned clinical studies. • Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department. • Responsible for protocol design and development, upon request. Provides input into protocol amendments. • Develops...СontratLe monde entierHoraires flexibles
