What are the responsibilities and job description for the Senior Clinical Project Manager position at Cynet Systems?
Job Description: Pay Range: $63.70hr - $68.70hr 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.
- Travels as necessary to aid in program facilitation.
- The position requires excellent communication skills, the ability to prioritize and work independently.
- Exposure to basic Project Management methods, knowledge of statistics would be an advantage as well as experience using the APOC i-STAT or equivalent system.
- Preference or other factors included in human rights legislation.
- Our diversity goals for recruitment, hiring, and retention are embedded in our corporate goals, and our diversity initiatives are supported by the highest level of the organization.
- We strongly believe that a diverse workforce fosters creative and innovative thinking throughout the organization.
- Creating an inclusive environment, where everyone is respected and valued, enables us to leverage our diversity as a business driver and strengthens our position as a global leader.
- Strives to promote and maintain an inclusive, high-performing culture that allows ll employees to reach their full potential and contribute to success.
- Post-secondary degree or diploma in Life Sciences, Biochemistry/Chemistry, Nursing, or equivalent.
- 5 years experience in managing clinical studies or equivalent product development programs.
- 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 is an asset.
- Ability to be creative in achieving objectives while ensuring compliance to regulatory requirements and policies.
Salary : $64 - $69
