Director of Clinical Project Management

7 days ago


Kirkland, Canada Novasyte Full time

Director, Global Project Leadership

IQVIA’s Directors within Global Project Leadership direct and manage the team responsible for clinical delivery of complex; global full service, multi-regional studies and/or programs as well as strategic decision-making responsibility for the project/program.

You will hold responsibility for the direction and management of portfolios and/or accounts from operational perspective. Day to day you will ensure that studies and/or programs are delivered on time whilst ensuring strong financial performance and customer satisfaction and in accordance with SOPs, policies and practices from pre-award to close-out.

This position has the scope to leverage your therapeutic expertise and combine with IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers.

KEY RESPONSIBILITIES
- Responsible for the management and delivery of large and/or complex studies or programs of studies. Serve as primary project/program/portfolio contact with customer and own relationship with key customer contact(s). Drive consistency and ensure financial success
- Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles
- Contribute to the development of the project delivery strategy for Request for Proposals (RFPs). Participate in bid defense preparations and lead presentations in partnership with business development for large, complex, multi-service, multi-region studies or programs
- Direct the execution of clinical studies while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures
- Set objectives for the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance
- Proactively manage strategic risk (positive and negative) and contingencies and lead problem solving and resolution efforts. Forecast and identify opportunities to accelerate activities to bring revenue forward
- Provide input to line managers of their project team members’ performance and support staff development including mentoring less experienced project team members
- May have the opportunity to manage between two and three direct reports

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
- Bachelor's degree in life sciences or related field
- 7+ years of prior experience, including substantial global project management experience
- Professional project management qualification (for example APM Chartered, PMP, Agile, Lean Six Sigma) is a strong advantage
- Viewed as a leading expert within the field by peers
- Requires extensive knowledge of multiple job areas obtained through advanced education and experience

Directeur responsable de la direction de projets internationaux

Les directeurs responsables de la direction des projets internationaux d’IQVIA dirigent et gèrent l’équipe responsable de la prestation clinique d’études ou de programmes multirégionaux complexes, à l’échelle mondiale, ainsi que de la prise de décision stratégique pour le projet/programme.

Vous serez responsable de la direction et de la gestion des portefeuilles et/ou des comptes dans une perspective opérationnelle. Vous vous assurerez au quotidien que les études ou les programmes sont exécutés à temps, tout en assurant un rendement financier solide et la satisfaction de la clientèle, et conformément aux PON, aux politiques et aux pratiques, de la phase préalable à l’attribution jusqu’à la phase de clôture.

Ce poste entend tirer parti de votre expertise thérapeutique et vous associer aux solutions d’IQVIA pour favoriser l’excellence opérationnelle et le leadership stratégique auprès de nos clients.

PRINCIPALES RESPONSABILITÉS
- Est responsable de la gestion et de la prestation d’études ou de programmes d’études importants et/ou complexes. Personne-ressource principale pour le projet/programme/portefeuille auprès du client et des personnes-ressources clés du client. Assure la cohérence et la réussite financière.
- Collabore avec d’autres groupes fonctionnels au sein de l’entreprise si nécessaire pour soutenir la réalisation des étapes importantes et gérer les problèmes et les enjeux liés à l’étude.
- Contribue à l’élaboration de la stratégie de l’exécution des projets pour les demandes de propositions (DP). Participe aux préparatifs de la présentation des offres et dirige les présentations en partenariat avec le développement des affaires pour des études ou des programmes de grande envergure, complexes, multiservices et multirégionaux.
- Assure l’exécution des études cliniques tout en optimisant la rapidité, la qualité et le coût de la prestation et en garantissant une utilisation cohérente des outils d’étude et des supports de formation, ainsi que la confo



  • Kirkland, Canada Pfizer Full time

    Use Your Power for Purpose At Pfizer, our mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. You will play a pivotal role in improving patients' lives by ensuring the accuracy, timeliness, and consistency of clinical data. Your work will bridge evidence-based medical decision support with colleagues...


  • Kirkland, Quebec, Canada IQVIA Argentina Full time

    Associate Director, COA Management - Patient Centered SolutionsOverviewIQVIA provides scientific solutions spanning clinical trials, real world evidence, and consulting in all areas of the drug product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the...


  • Kirkland, Canada Pfizer Full time

    ROLE SUMMARY As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Clinical Data Scientist (CDS) is responsible for timely and high-quality data management deliverables supporting the Pfizer portfolio. The CDS delivers asset level information strategies...


  • Kirkland, Canada Pfizer Full time

    ROLE SUMMARY: Global Product Development (GPD) supports clinical development across Pfizer and late-stage development of medicines. Every year, GPD partners with thousands of global participants, health systems and HCPs in our work to bring new medicines to market for the patients that we serve. In coordination with GPD and COE colleagues, provide...


  • Kirkland, Quebec, Canada Pfizer Full time

    This critical role involves leading efforts to safeguard Pfizer's reputation by ensuring adherence to our protocols at clinical trial sites and among healthcare professionals. You will leverage your expertise in drug development, clinical trials, and global operations to manage third-party entities, like site organizations, and drive quality delivery.Your...


  • Kirkland, Quebec, Canada Pfizer Full time

    About the PositionWe are seeking an experienced professional to join our team as the Global Site Partnerships Director. In this role, you will be responsible for leading activities to protect Pfizer from reputational risk resulting from the conduct of work/collaboration with HCPs and Clinical Trial Sites/Organizations.About the Team:The Optimization,...


  • Kirkland, Canada IQVIA Full time

    **Job Overview** Perform, manage and co-ordinate activities for complex opportunities/ projects. Utilize multiple data sources to perform analysis, formulate recommendations and present to internal and external stakeholders. Train and mentor junior staff and country leads. Make recommendations and lead process improvements. **Essential Functions** -...


  • Kirkland, Quebec, Canada IQVIA LLC Full time

    Job OverviewThe Senior Biostatistician plays a critical role in providing statistical support for drug development programs in phases 2 or 3 with efficacy and safety endpoints. This position requires collaboration with multidisciplinary project teams to establish project timelines, provide statistical input to study synopses and protocols, and write or...


  • Kirkland, Canada Novasyte Full time

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...


  • Kirkland, Quebec, Canada IQVIA LLC Full time

    **Job Overview:**IQVIA LLC is seeking a highly skilled Statistical Expert to support our clinical trials. As a key member of our team, you will provide statistical input to study synopses and protocols, collaborate with project teams to establish project timelines, and manage internal and CRO project activities.Responsibilities:Collaborate with...

  • IT Project Manager

    2 weeks ago


    Kirkland, Canada IQVIA Full time

    **Gestionnaire de projet informatique** **Description du travail** Planifier et diriger les activités d'équipes interdisciplinaires affectées à de multiples projets informatiques afin de répondre aux exigences des équipes commerciales dans le cadre du plan d'exécution des projets, de leurs budgets, et le respect de leurs contrats. Cela inclut la...

  • IT Manager

    2 weeks ago


    Kirkland Lake, Canada Corporation of the Town of Kirkland Lake Full time

    The Corporation of the Town of Kirkland Lake is seeking a **Information Technology Manager** Full-Time / Non-Union **Position Overview**: - The Information Technology (IT) Manager reports to the Director of Corporate Services, and is responsible for the conceptualization, planning, purchase, management and renewal of the Corporation’s information...


  • Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of...


  • Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of...


  • Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration:Track (e.g. essential documents) and report (e.g. Safety Reports)Ensure collation and distribution of study tools...


  • Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration:Track (e.g. essential documents) and report (e.g. Safety Reports)Ensure collation and distribution of study tools...


  • Kirkland, Canada Pfizer Full time

    Status : Regular, Full-Time Statut : Régulier, temps plein (Français à suivre) Global Product Development (GPD) supports clinical development across Pfizer and late-stage development of medicines. Every year, GPD partners with thousands of global participants, health systems and HCPs in our work to bring new medicines to market for the patients that we...


  • Kirkland, Quebec, Canada Pfizer Full time

    Job OverviewWe are seeking an experienced professional to join our team as the Clinical Trial Oversight Specialist. In this role, you will be responsible for leading activities to protect Pfizer from reputational risk resulting from the conduct of work/collaboration with HCPs and Clinical Trial Sites/Organizations.About the Team:The Site Intelligence,...


  • Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: - Track (e.g. essential documents) and report (e.g. Safety Reports) - Ensure collation and distribution...


  • Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of study...