This role will be perfect for you if: - You are looking to contribute your expertise to the growth of a specialized CRO - You are a hands-on leader - You want to be involved in program management as well as line management RESPONSIBILITIES - Oversees a portfolio or program of projects and the Project Managers assigned to operationalize the awarded studies. - Ensures all studies within a program or portfolio are conducted to reflect the therapeutic or client specific requirements. - Represents company to the customer, ensuring satisfaction levels are maintained and program deliverables are communicated effectively. - Ensures the study is progressing according to internal and Customer quality standards, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) or appropriate regulatory requirements, and International Conference on Harmonization (ICH) guidelines to fulfil all federal and local regulations. - Oversees the management of the executed contract and financial aspects of assigned projects, including reviewing study budgets and expenses. - Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. - Ensures and maintains an in depth therapeutic and/or client specific knowledge and expertise for the assigned portfolio. - Applies study specific learning across assigned portfolio of studies/clients. - Leads and ensures consistency in contingency planning and risk mitigation strategies to ensure successful delivery. - May lead operational input to proposal development and pricing including proposed operations strategy - Drives performance improvement, operational efficiencies and innovative strategies - May provide line management oversight and contribute to leadership of Project Management as an operational and therapeutic area expert Requirements: IDEAL PROFILE Education - Bachelor of Science in a relevant discipline. - A Master’s degree is an asset. - PMP or PRINCE2 Certification is an asset Experience - At least 15 years industry experience and a minimum of 5 years at a CRO - At least 10 years of clinical project management experience, including management of all projects phases from start up to closure, management of all functional services, vendor management. Experience with mid-size and large studies (>10-15 countries) in multiple regions (NA, SA, APAC, MENA, Europe) is desirable. - Experience leading concurrent multi-centered, multinational phase III clinical trials including project budget financial tracking and forecasting - Substantial experience in project supervision, mentoring and coaching project managers - Substantial experience with business development tasks, such as development of proposals, client presentations, bid defense meetings, and the like - Participation in mentoring and coaching of a representative number of project managers - Line management experience is desirable - Dermatology experience is an asset Knowledge and skills - Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines Our company: At Indero, you will work alongside brilliant and driven colleagues. Our core values are integrity, commitment, and teamwork. We offer a stimulating work environment with attractive opportunities for growth and advancement. As a Project Director, you will be eligible for the following perks: - Flexible schedule - Vacation - Home-based position - Ongoing learning and development opportunities About Indero Indero is a contract research organization (CRO) specialized in dermatology and rheumatology. Since its founding in 2000, our organization has built a strong reputation for delivering high-quality research and services that exceed client expectations. Based in Montreal, Indero continues to grow and expand across North America and Europe, including operations in Romania. Indero is committed to providing equitable treatment and equal opportunity to all individuals. We will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.