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Oakville

    Temporary Associate - Oakville, ON, Canada - Innomar Strategies

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    Full time
    Description

    If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.

    Review of source data documents (includes visit report/PIR review) and triaging adverse event information and product quality complaints as per client needs;
    Data entry and submission of adverse event information and product quality complaints into program specific databases;
    Sorting and filing of incoming documents;
    Perform quality check on adverse event reports as directed by the work instructions
    Assist with and/or perform source data verification checks
    Screening medical and scientific literature for safety information
    Preparation of Reconciliation (weekly, monthly etc.) Transcription, translations and redaction activities
    Preparation and conducting solicited follow-up letters and data clarifications
    The Drug Safety Associate will also be assigned other duties and tasks as required from time to time
    A diploma or degree with a concentration in Life Sciences is a strong asset;
    ~1-3 years experience in Medical Information, Clinical Research or Drug Safety or equivalent and related experience in pharmacy or pharmaceutical fields;
    ~ Knowledge of Pharmacovigilance industry including up to date knowledge of; pharmacovigilance guidelines of Health Canada, US FDA, EMEA and ICH;
    ~ Experience in the medical and/or pharmaceutical field(s), medical terminology is an asset;
    ~ Bilingual, English/French is an asset.
    ~ Able to work any 8-hour shift between 8:00 AM-8 PM, if necessary

    Ability to communicate effectively both orally and in writing
    Computer skills (including knowledge of Microsoft Word, Excel, PowerPoint and other Office Programs)
    Good internet required for remote work

    The successful candidate will (requirement)/may (asset) have daily contacts with unilingual English-speaking customers, patients or peers from cross-functional teams.

    In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness.

    This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave.

    To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.

    .
    Full time Our team members are at the heart of everything we do.

    If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.

    Examen des documents de données sources (y compris l'examen des rapports de visite RPP/PIR) et triage des informations sur les événements indésirables et des plaintes sur la qualité des produits en fonction des besoins des clients;
    Saisie des données et saisie des informations sur les événements indésirables et des plaintes relatives à la qualité des produits dans les bases de données spécifiques au programme;
    Effectuer un contrôle de la qualité des rapports d'événements indésirables conformément aux instructions de travail;
    Assister ou effectuer les tâches de vérification des données sources;
    Activités de transcription, de traduction et de rédaction;
    Préparation et réalisation de lettres de suivi sollicitées et de clarifications de données;
    L'associé de la pharmacovigilance se verra également confier d'autres fonctions et tâches au besoin, de temps à autre.
    Un diplôme ou un diplôme avec une concentration en sciences de la vie est un atout important;
    Connaissance de l'industrie de la p harmacovigilance, y compris une connaissance à jour des directives de pharmacovigilance de Santé Canada, de la FDA, de la EMEA et de l'ICH;
    Une expérience dans le domaine médical ou pharmaceutique est un atout;
    Le bilinguisme (anglais/français) est un atout;
    De solides aptitudes d'analyses;
    Microsoft Word, Excel, PowerPoint et d'autres programmes Office);
    Un bon accès à l'Internet est nécessaire pour le télétravail.
    Review of source data documents (includes visit report/PIR review) and triaging adverse event information and product quality complaints as per client needs;
    Data entry and submission of adverse event information and product quality complaints into program specific databases;
    Sorting and filing of incoming documents;
    Perform quality check on adverse event reports as directed by the work instructions
    Assist with and/or perform source data verification checks
    Screening medical and scientific literature for safety information
    Preparation of Reconciliation (weekly, monthly etc.) Transcription, translations and redaction activities
    Preparation and conducting solicited follow-up letters and data clarifications
    The Drug Safety Associate will also be assigned other duties and tasks as required from time to time
    A diploma or degree with a concentration in Life Sciences is a strong asset;
    ~1-3 years experience in Medical Information, Clinical Research or Drug Safety or equivalent and related experience in pharmacy or pharmaceutical fields;
    ~ Knowledge of Pharmacovigilance industry including up to date knowledge of; pharmacovigilance guidelines of Health Canada, US FDA, EMEA and ICH;
    ~ Experience in the medical and/or pharmaceutical field(s), medical terminology is an asset;
    ~ Bilingual, English/French is an asset.
    ~ Able to work any 8-hour shift between 8:00 AM-8 PM, if necessary

    Ability to communicate effectively both orally and in writing
    Computer skills (including knowledge of Microsoft Word, Excel, PowerPoint and other Office Programs)
    Good internet required for remote work

    The successful candidate will (requirement)/may (asset) have daily contacts with unilingual English-speaking customers, patients or peers from cross-functional teams.

    Le candidat retenu aura/pourrait avoir des contacts quotidiens avec des clients, des patients ou des pairs unilingues anglophones d'équipes interfonctionnelles.

    In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness.

    This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave.

    To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.


    Full time Affiliated Companies:

    Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

    Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

    AmerisourceBergen is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements.

    Accessibility Policy
    When requested, AmerisourceBergen will accommodate people with disabilities during the recruitment, assessment and hiring processes and during employment.

    Cencora is a leading global pharmaceutical solutions company that is committed to improving the lives of people and animals everywhere.

    We connect manufacturers, providers, and patients to ensure that anyone can get the therapies they need, where and when they need them.

    We work together every day to help our partners bring their innovations to patients worldwide, creating unparalleled access and impact at the center of health.

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