Description
The Project Director is responsible for overseeing the conduct of a program or portfolio of clinical studies or large global multicenter trials with substantial budgets. The portfolio may include studies for specific clients or a group within the same therapeutic area or indication for multiple clients. The Project Director manages Project Managers (PMs) handling projects of varying sizes and complexities, from single-service studies to large, multi-protocol, global projects, or a portfolio of projects. This role involves leading operational contributions to proposal development and business activities at a project level, applying therapeutic and project management expertise with minimal oversight.
This role will be perfect for you if :
- You want to contribute your expertise to a growing, specialized CRO
- You are a hands-on leader
- You are interested in program management as well as line management
Responsibilities
Oversee a portfolio or program of projects and the Project Managers responsible for operationalizing studies.Ensure all studies meet therapeutic or client-specific requirements.Represent the company to clients, maintaining satisfaction and effective communication of program deliverables.Ensure studies comply with internal and client quality standards, SOPs, GCPs, regulatory requirements, and ICH guidelines.Manage contract execution and financial aspects, including reviewing budgets and expenses.Track project progress using timelines and analysis tools.Maintain in-depth therapeutic or client-specific knowledge for the portfolio.Apply learnings across studies and clients within the portfolio.Lead contingency planning and risk mitigation strategies for successful delivery.Contribute to proposal development and pricing strategies.Drive performance improvements, operational efficiencies, and innovative strategies.Provide line management oversight and contribute to leadership within Project Management.Requirements
Education
Bachelor of Science in a relevant discipline.A Master’s degree is an asset.PMP or PRINCE2 Certification is an asset.Experience
Minimum 15 years of industry experience, with at least 5 years at a CRO.At least 10 years of clinical project management experience, managing all project phases across multiple regions and large studies.Experience leading multi-center, multinational phase III trials, including budget management.Experience mentoring and coaching project managers.Business development experience, including proposals and client presentations.Line management experience is desirable.Dermatology experience is an asset.Knowledge and Skills
Strong knowledge of GCPs, FDA, and Health Canada regulations.Our Company and Work Environment
At Indero, you will work with talented colleagues in a culture that values collaboration, innovation, reliability, and responsiveness. We offer a stimulating environment and career growth opportunities.
This position offers perks such as flexible work schedules, a home-based setup, and ongoing learning and development.
About Indero
Indero is a CRO specializing in dermatology and rheumatology, established in 2000, with a reputation for high-quality research and services. Based in Montreal, we are expanding across North America and Europe.
Indero is committed to equitable treatment and provides accommodations during recruitment for applicants with disabilities. Only applicants authorized to work in Argentina will be considered.
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