- Compensation: CAD 135000 - CAD 150000 - yearly
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.
Your responsibilities will include:
- Managingsmall (<5 countries and/or limited services) projects under direct or general supervision, with primary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget
- Performingregional lead's or project co-manager's role in complex international projects/programs with the secondary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget.
- Adheringto and promotingprinciples of delivery and service in dealing with PSI customers.
- Leadingproject teams
- Training, mentoring, and coaching Lead CRAs, Senior CRAs, CRAs, Project Coordination Associates (PCAs) and Site Management Associates (SMAs)
- Participating in feasibility research
- Supporting business development tasks such as proposals, client presentations, bid defense meetings, etc.
- Implementing company standard practices and complying with intradepartmental procedures
Qualifications
- Bachelor's degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities. Equivalency is defined as a minimum 5 years of experience gained in pharmaceutical/healthcare industry and clinical research.
- At least 5-year industry experience in clinical research
- Atleast 2-year recent clinical research experience in the capacity of project manager/equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.).
- Regional clinical project management experience, including management of all project services from startup to closure
- Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
- Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships
Additional Information
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.