Average salary: $88,222 /yearly
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$65k - $70k per year
...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...SuggestedWork at office$99.2k - $124k per year
...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...SuggestedInternshipWork at officeLocal areaWorldwide$30 - $48 per hour
...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...SuggestedHourly payPart timeImmediate start$57k - $71k per year
...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...SuggestedInternshipWork at officeShift work$55k - $65k per year
...experience) ________________________________________________________________________________ POSITION SUMMARY: The Pharmacovigilance (PV) and Quality Associate is responsible for supporting and maintaining all pharmacovigilance and quality assurance activities...SuggestedPermanent employmentFull timeWork at officeMonday to friday- ...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...SuggestedInternshipWork at office
- ...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...SuggestedWork at office
- ...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...SuggestedHourly payPermanent employmentFull timeRemote workMonday to fridayFlexible hours
- ...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...SuggestedFull timeImmediate startRemote work
- ...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...SuggestedFull timeWorldwide
- ...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...SuggestedContract workFixed term contractImmediate startRemote workHome office
- ...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...SuggestedLong term contractPermanent employmentContract workTemporary workFixed term contractWork at officeLocal areaImmediate start3 days per week
- ...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...SuggestedLong term contractPermanent employmentContract workTemporary workFixed term contractWork at officeImmediate start3 days per week
- ...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...SuggestedOngoing contractContract workInterim roleLocal areaImmediate startRemote work
- ...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...SuggestedContract workImmediate start
$125.12k - $173.7k per year
...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...Local areaRelocation packageFlexible hours- ...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...InternshipWork at office
$67.05k - $89.4k per year
...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...Full timeContract workRemote workMonday to fridayFlexible hoursKelly Services
Canadaa month ago- ...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...FreelanceLocal area
- ...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...InternshipWork at officeWork from homeWorldwide
- ...(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/...Full timeContract workWork from home
- ...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...Remote jobPermanent employment
- ...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...ApprenticeshipWork at officeImmediate startFlexible hours
$75k - $130k per year
...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...Work at officeLocal areaRemote workWork from home- ...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...Long term contractPermanent employmentContract workTemporary workFixed term contractWork at officeFlexible hours3 days per week
- ...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...RemplacementPermanent employmentFull timeContract workRemote workWork from homeFlexible hoursShift work
- ...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...Full time
- ...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...Contract workInterim roleLocal areaImmediate startRemote work
- ...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...Temporary workWork at officeWorldwideFlexible hours
$146k - $277k per year
...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...Contract workWorldwideFlexible hours
