Consultant Project Manager

12 hours ago

Kirkland, Canada IQVIA Full time

From research to real world, IQVIA weaves together the technologies, resources, and expertise our customers need to rise to the next opportunity. IQVIA uses Human Data Science — the integration of data science, technology, and human science — to help customers address both current needs and future opportunities. To get there, to make Human Data Science work, for you, you need a seamless integration of unparalleled data, advanced analytics, transformative technology, and deep domain expertise.

IQVIA is a world leader in using data, technology, advanced analytics and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

The Real World Solutions team in Canada supports the needs of clients in market access strategy, health economics and outcomes research, insights from multiple healthcare databases across Canada, and Real World Evidence generation undertaken through innovatively designed local Phase IV studies.

We offer a local Canadian service for clients using a highly skilled local agile team. We have strong technological solutions for working with physicians and patients, and yet maintain a simple agile infrastructure to ensure we provide that local touch to clients.

**Functional responsibilities**

Lead the delivery of projects for our clients, the pharmaceutical industry, governments and academic centres in Canada, focusing on retrospective and prospective real-world evidence studies.

Unlike the role of a traditional Clinical Project Manager, the Consultant Project Manager leads an agile local team throughout the full continuum of the study - from start-up, investigator meetings, client calls, data collection, right through to close-out and dissemination of the study results.

**Essential Functions**
- Project Manage Late Phase Research projects for the Canadian local market.
- Lead an agile local team, as well as cross-functional support teams, in the delivery of quality real world studies.
- Ensure effective and efficient planning, organization, and execution of studies and study budgets. Tasks include, but are not limited to:

- Assist with the review and analysis of client requirements or problems
- Assist in the development of proposals and client solutions
- Run client meetings and/or meetings with key opinion leaders
- Lead implementation of the project plan/managing budget
- Liaise between internal and external vendors
- Assist in the development of detailed study documentation and specifications
- Oversee and ensure quality of deliverables
- Ensure accurate adherence to Standard Operating Procedures and quality processes
- Manage study risk mitigation
- Prepare reports, i.e., design/structure and completion of presentations that are appropriate to the characteristics or needs of the audience
- Maintain Study Master File
- May be assigned additional responsibilities, as needed
- Proactively develop a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.

**Education/Qualifications**
- Master of Science, PhD, MD, PharmD (or equivalent experience in industry)
- Epidemiology experience or an area of study advantageous
- Knowledge and understanding of the process of undertaking Real World or observational studies
- Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline
- Knowledge of consulting methods, tools and techniques, related to one’s functional area

**Experience**:
You will typically have been working in one of the following environments for three to four years:

- An experienced and qualified Clinical Project Manager in academia, hospital, other life-science function, or a CRO
- A Project Manager in the Pharmaceutical Industry
- Previous experience in a study or clinical trial support role

**Technical skills and knowledge (assets)**:

- Understanding of and interest in the Canadian and international health care environment, and evolving industry standards/challenges
- Good understanding of outcomes research theory, and practical knowledge of research project implementation
- Familiarity with or an understanding of site management activities is a bonus
- High level of literacy - able to write reports in clear, accurate and concise language; experience with medical writing is a bonus
- Numerate with good quantitative skills
- Conducting analyses in databases and/or registries
- Longitudinal patient level data analysis
- Competency using MS Office products including Word, PowerPoint and Excel is required
- Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines trained
- Certifie

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