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    Director Of Project Development H/F - Montréal, QC, Canada - Caprion Biosciences Inc.

    Caprion Biosciences Inc.
    Caprion Biosciences Inc. Montréal, QC, Canada

    1 week ago

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    Description
    Director, Assay Development
    CellCarta, a Contract Research Organization, is hiring a Director of Assay Development to join our dynamic team.

    As the Director of Assay Development, you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards.

    The Director of Assay Development is responsible for the development of flow cytometry assays that meet the intended purpose in the scope of the clinical trial(s).

    They manage and mentor a team of scientists and research assistants for the development of custom assays, standard panel set-up, assay characterization and fit-for-purpose validation of exploratory studies, as well as provide guidance for effective testing design and troubleshooting of technical issues encountered in development.

    They provide scientific/technical leadership within the development team, as well as the scientific team (principal scientists), within CellCarta organization, at scientific meetings and with CellCarta customers.

    The Director of Assay Development may be required to lead or participate in the implementation of new technologies as well as enhance existing or implement new flow cytometry protocols.

    Overseesscientific/technical designanddeliveryoftheprojects according to set timelines
    Ensures that the assignment of projects is appropriate,based on the technical skill set of the scientist
    Ensuresthatthedevelopmentas wellaspanelset-upintermsof testing design is performed appropriately by the scientists
    Provides oversight tothetechnical designas well asconclusions to the data
    Ensures that the planning of studies is efficient, and deliverables are met
    Leads troubleshooting activities along with the development scientist by assisting and mentoring members of the development team
    Assess and implements a streamlined approach to assay development by identifying areas of improvement and leads the effort of optimization
    Review and approve the documentation (e.g. workplans, reports) from development studies
    Actively supports Business Development with new client meetings for the scientific aspect and assay design of future work as well as scientific meetings
    Actively participates in assay plan design and scientific writing of client proposals
    Attends scientific conferences as required
    Interact with the Data Analysis Unit and Principal Scientists in the development of new assays as per client needs, including the assay validation phase
    Responsible of performing annual performance review of staff directly undersupervision
    PhD diploma in Immunology, with 3 years or more of post-doctoral training.
    Demonstrated understanding of drug development (discovery, preclinical and clinical phases).
    ~ Workingunderstandingofbiomarkerassaysin supportofdrug development.
    ~ 10 years)experience withflowcytometrytechniques and applications in the field of immune monitoring including assay design as well as handling complex data set of multi-color panels.
    ~ Expert level proficiency in working with third party flow cytometry data analysis packages and Microsoft Office products.
    ~ Strong knowledge of current validation requirementsforcellbased analysis.
    ~ Strong knowledge and understanding of GLP/CAP/CLIA regulations and other regulatory guidelines.
    ~ English and French proficiency (written and spoken) is required.
    ~4 years of experience in project management.
    ~ Critical and creative thinker.
    ~ Advanced level of understanding and analytical skills to interpret data and draw conclusions.
    ~ Ability to present high-level summaries to senior management.
    ~ Must be willing to supervise activities in Bio Safety Level (BSL) 1 or 2 facilities where biological samples may be either naturally or experimentally infected with potentially hazardous viruses such as HIV, HCV, or CMV.

    Dialogue Telemedicine Service and Employee Assistance Program (EAP);
    CellCartais a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry.

    Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials.

    The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.

    Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy.

    Join us as we make an impact on patient therapy

    The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc.

    and its affiliates (collectively, "CellCarta").

    The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

    This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV.

    CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application.

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