Director of Assay Development

Director, Assay DevelopmentAre you looking to make your next career move? 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. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today and take the first step towards an exciting new career with CellCarta!SummaryThe 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.ResponsibilitiesOverseesscientific/technical designanddeliveryoftheprojects according to set timelinesEnsures that the assignment of projects is appropriate,based on the technical skill set of the scientistEnsuresthatthedevelopmentas wellaspanelset-upintermsof testing design is performed appropriately by the scientistsProvides oversight tothetechnical designas well asconclusions to the dataEnsures that the planning of studies is efficient, and deliverables are metLeads troubleshooting activities along with the development scientist by assisting and mentoring members of the development teamAssess and implements a streamlined approach to assay development by identifying areas of improvement and leads the effort of optimizationAssesses and implements new protocols for flow cytometry assays that maintain CellCarta within industry standardsStayabreastofcurrentbestpracticesin flowcytometryand immunologyReview and approve the documentation (e.g. workplans, reports) from development studiesActively supports Business Development with new client meetings for the scientific aspect and assay design of future work as well as scientific meetingsActively participates in assay plan design and scientific writing of client proposalsAttends scientific conferences as requiredParticipates in the preparation of presentations and publications in collaboration with clients when possibleInteract with the Data Analysis Unit and Principal Scientists in the development of new assays as per client needs, including the assay validation phaseResponsible of performing annual performance review of staff directly undersupervisionEducationPhD diploma in Immunology, with 3 years or more of post-doctoral training.Minimum of 5 years of experience in Pharma/CRO industry.Experience and Skills RequiredDemonstrated understanding of drug development (discovery, preclinical and clinical phases).Workingunderstandingofbiomarkerassaysin supportofdrug development.Longstanding(>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 people management or demonstrated ability to manage people.>4 years of experience in project management.Demonstrated ability to lead a team by gathering consensus and then make decision on the path forward.Works methodically and systematically.Critical and creative thinker.Advanced level of understanding and analytical skills to interpret data and draw conclusions.Communicate clearly and confidently and has excellent interpersonal and teaching skills.Ability to manage tense situations constructively and maintain good relationship with internal/external clients.Ability to present high-level summaries to senior management.Excellent time management and organizational skills to meet deadlines in a fast-paced, changing environment.Excellent record keeping, attention to detail.Working ConditionsMust 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.BenefitsWe offer a wide range of benefits including:Competitive Wages;Vacation and Personal Days;Comprehensive Group Insurance Plans;RRSP Contribution with Employer Matching;Employee Annual Incentive Plan (EAIP);Dialogue Telemedicine Service and Employee Assistance Program (EAP);OPUS & Cie Contribution;Parking Reimbursement;Referral Program;Career Advancement Opportunities.About CellCartaCellCartais 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. We make a difference in the lives of patients around the world!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.CellCarta will only process that information which is necessary to evaluate your application. 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. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. 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. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contactprivacy@cellcarta.com.

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