Senior Clinical Project Manager
at PSI CRO
GMA, QC, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Sep, 2024 | Not Specified | 25 Jun, 2024 | 5 year(s) or above | Clinical Research,Closure,Training,Vendor Management | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Company Description
PSI is a leading Contract Research Organization with more than 28 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
Project Management
- Management of medium-sized (5-15 countries and/or full service) or large (>15 countries, full service) projects/programs under general supervision, with primary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget
- Adherence to and promotion of principles of delivery and service in dealing with PSI customers
Project Supervision
- Project Supervision of small (<5 countries and/or limited services) projects/programs
- Supervisory responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget, adhering to and promoting principles of delivery and service in dealing with PSI customers
- Primary escalation contact for PSI customers, vendors, project teams and representatives of other functional areas for all project-related issues
Corporate/Departmental Assignments
- Training, mentoring and coaching of Regional Leads and (Lead) Project Managers
- Participation in feasibility research
- Assistance in business development tasks, such as development of proposals, client presentations, bid defense meetings, and the like
- Implementation of company standard practices and compliance with intradepartmental procedure
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 7 years of industry experience in clinical research
- At least 4 years of global (project-level) clinical project management experience, including management of all projects phases from startup to closure, management of all functional services, vendor management
Additional Information
All your information will be kept confidential according to EEO guidelines
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:5.0Max:7.0 year(s)
Other Industry
Site Engineering / Project Management
Other
Graduate
Proficient
1
Greater Montreal Area, QC, Canada