Chef de Projet, Direction de Projet Global / Project Leader, Global Project Leadership

IQVIA Argentina; Montreal; On-site; CAD 90,000 - 130,000; Full time

Job summary

IQVIA Argentina is seeking a Project Leader to manage cross-functional teams and ensure project delivery and quality within the Research & Development Operations. This role requires extensive clinical research experience and the ability to manage project budgets while collaborating with various experts. Successful candidates will have a strong background in life sciences and project management.

Qualifications

• 5-7 years’ clinical research experience.
• Minimum 4 years prior project management experience.
• In-depth therapeutic knowledge in Immunology, CVRM, or Oncology.

Responsibilities

• Lead global cross-functional project team delivery.
• Develop study management plans and ensure compliance.
• Manage study budget proactively.

Skills

Project Management

Clinical Research

Risk Management

Education

Bachelor's degree in life sciences

Job description

The Project Leader role requires you to manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best in class technology and data analytics.

Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager as an expert in start-up.

This is an important and high-profile role within our Research & Development Operation and IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.

Typically assigned to one or two projects, or a program, responsibilities might include :

• Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope.
• Serving as the primary contact with the customer for progress and governance.
• Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures.
• Anticipating risk and implementing mitigation strategies.
• Managing study team assignments, accountability and resource requirements.
• Ensuring the study budget is managed proactively including scope changes and financial systems are accurate.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Bachelor's degree in life sciences or related field and 5-7 years’ clinical research experience.
• Global project management experience within the drug development industry, with previous CRO experience is ideal. Minimum 4 years prior project management experience and experience in clinical operations; or equivalent combination of education, training and experience.
• In depth therapeutic knowledge in Immunology, CVRM, or Oncology.

IQVIA is proud to be an equal opportunity employer and we are committed to creating a diverse and inclusive environment. We do not discriminate on the basis of any applicable prohibited ground of discrimination, including but not limited to race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability. Accommodations for applicants with disabilities are available at all stages of the recruitment process upon request. If you have a physical impairment or a disability that requires an accommodation, we encourage you to disclose this during the recruiting process so that IQVIA can appropriately accommodate you.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https : / / jobs.iqvia.com .

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