Chef de projet, Opérations d'études, Cronos, Kirkland
Chef de projet, Opérations d'études, Cronos, Kirkland
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Kirkland, Canada
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Publiée: hier
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Description
Job Overview
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. They are essential members of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management focuses on project delivery, productivity and quality, resulting in strong financial performance and customer satisfaction.Responsibilities
Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies. May be responsible for delivery and management of smaller, less complex, regional studies. Develop integrated study management plans with the core project team.Accountable for the execution of clinical studies per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures. Set objectives of the core project team and/or sub‑team(s) according to agreed contract, strategy and approach, effectively communicate and assess performance.Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles. Monitor progress against contract and proactively prepare/present project and sub‑team information to stakeholders internally and externally. Manage risk and contingencies proactively and lead problem‑solving and resolution efforts.Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and planning/implementing appropriate corrective and preventative action plans. Serve as primary or backup project contact with customer, owning the relationship with key customer contacts and collaborating with business development representatives as needed.Build and lead the cross‑functional project team, managing cross‑collaboration and overall project delivery to support milestone achievement and manage study issues and obstacles. Ensure the financial success of the project. Forecast and identify opportunities to accelerate activities to bring revenue forward.Identify changes in scope and manage change‑control process as necessary. Identify lessons learned and implement best practices. Act as primary contact for vendors, leading project vendor management and related activities as required. Adopt corporate initiatives and changes and serve as a change advocate when necessary.Provide input to line managers on the performance of project team members relative to project tasks. Support staff development and mentor less experienced project team members on assigned projects to support their professional development. Qualifications
College degree in Life Sciences or related field. More than 7 years of prior clinical research experience, including at least 5 years of project management experience in a global environment and client‑facing role. Strong written and verbal communication skills, excellent presentation abilities, and good command of English.Strong problem‑solving skills. Ability to motivate and coordinate teams to deliver results within quality and timeline metrics, monitoring and managing performance, and providing constructive feedback. Ability to make decisions and bring clarity to disparate information to inform actions and drive results.EEO Statement
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.
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Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. They are essential members of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management focuses on project delivery, productivity and quality, resulting in strong financial performance and customer satisfaction.Responsibilities
Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies. May be responsible for delivery and management of smaller, less complex, regional studies. Develop integrated study management plans with the core project team.Accountable for the execution of clinical studies per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures. Set objectives of the core project team and/or sub‑team(s) according to agreed contract, strategy and approach, effectively communicate and assess performance.Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles. Monitor progress against contract and proactively prepare/present project and sub‑team information to stakeholders internally and externally. Manage risk and contingencies proactively and lead problem‑solving and resolution efforts.Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and planning/implementing appropriate corrective and preventative action plans. Serve as primary or backup project contact with customer, owning the relationship with key customer contacts and collaborating with business development representatives as needed.Build and lead the cross‑functional project team, managing cross‑collaboration and overall project delivery to support milestone achievement and manage study issues and obstacles. Ensure the financial success of the project. Forecast and identify opportunities to accelerate activities to bring revenue forward.Identify changes in scope and manage change‑control process as necessary. Identify lessons learned and implement best practices. Act as primary contact for vendors, leading project vendor management and related activities as required. Adopt corporate initiatives and changes and serve as a change advocate when necessary.Provide input to line managers on the performance of project team members relative to project tasks. Support staff development and mentor less experienced project team members on assigned projects to support their professional development. Qualifications
College degree in Life Sciences or related field. More than 7 years of prior clinical research experience, including at least 5 years of project management experience in a global environment and client‑facing role. Strong written and verbal communication skills, excellent presentation abilities, and good command of English.Strong problem‑solving skills. Ability to motivate and coordinate teams to deliver results within quality and timeline metrics, monitoring and managing performance, and providing constructive feedback. Ability to make decisions and bring clarity to disparate information to inform actions and drive results.EEO Statement
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.
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Informations clefs
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Nom de l’entrepriseIQVIA
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Titre de posteChef de projet, Opérations d'études, Cronos
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Chef de projet, Opérations d'études, Cronos est visible sur Locanto dans la rubrique Kirkland Ingénierie.
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