Permanent Clinical Project Manager

LocationOttawa
Job CategoryProfessional Consulting
SP-ID29857
Position TypeFull Time
Application Deadline June 30, 2021
Experience Required5+ years
Job DurationPermanent
Education RequiredBachelors

Location: OTTAWA
 
 
Qualifications:
 
Post-secondary degree or diploma in Life Sciences, Biochemistry/Chemistry, Nursing, or equivalent
6+ years’ experience in managing clinical studies or equivalent product development programs is mandatory
Experience in in vitro diagnostic/medical device related studies is an asset.
Knowledge of Good Clinical Practice and regulations governing in vitro diagnostics/medical devices is desirable
Advanced skills in project planning and management, judgment, decision-making, and problem solving
Working knowledge of new product development methodologies an asset
Ability to be creative in achieving objectives while ensuring compliance to regulatory requirements and policies
Responsibilities:
 
Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations
Oversees development of clinical documents, including clinical plans, protocols, forms, and reports
Manages team to prepare for clinical study initiation, execution and close out activities
Monitors and reports progress of clinical studies and follows up with team members and line managers when issues develop
Communicates and works with cross-functional teams to resolve issues that arise during clinical studies
Ensures consistency of clinical study and processes across clinical trials
 
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