Clinical and R&D Manager Contracts!

LocationOttawa
Job CategoryProfessional Consulting
SP-ID26864
Position TypeContract
Application Deadline January 31, 2021
Experience Required3 years
Job Duration1 year
Education RequiredBachelors

We are looking for a self-motivated, flexible project manager to work in a dynamic environment supporting new product development/business continuity/infrastructure projects. Working as part of the Program Management Office, your responsibilities may include, but are not limited to:
Supporting the Program Manager and Program Lead in meeting project deliverables in a timely fashion. 
Maintaining an understanding of project deliverables, risks, issues, constraints, and scope to ensure project is delivered on time and within budget.
Forecasting project requirements and providing information to relevant stakeholders.
Ensuring project teams are aware of deliverables, priorities and timelines.
Coordinating/managing day-to-day activities, tracking deliverable status, monitoring resource requirements.
Measuring project performance to identify areas for improvement.
Actively elevating to Program Manager for resolution, any developing issues that compromise the published timelines and deliverables.
Supporting the development and maintenance of detailed program plans as required.
Ensuring a positive work environment.
To be considered for this position, you will have the following education, skills, and abilities:
Post-secondary degree or diploma in Engineering or Physical Sciences.
3-5 years’ experience in project management, ideally in medical device or pharmaceutical industries.
Skills in project planning and management, judgment, decision-making, and problem solving.
Strong influencing skills, interpersonal skills and organizational skills.
Excellent communication and ability to translate complex information to multiple levels of stakeholders.
Ability to be creative in achieving objectives while assuring compliance to internal and external requirements.
Experience in project management, preferably in an R& D or product development
environment.
Experience in an FDA regulated environment is an asset.
If you are interested in this role, please contact
a.valencia@maxsys.ca
Only those who are qualified for the role will be contacted
MAX112