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Join Our Talent Community - Senior Project Manager, Oncology - Remote
Company | Precision Medicine Group |
Address | Montreal, Quebec, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Pharmaceutical Manufacturing |
Expires | 2023-08-22 |
Posted at | 10 months ago |
Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
- You strive in developing shipmates to be their best; knowing that all have a unique skill set to bring to your team
- You welcome icebergs that come into your path for you are the Captain of the ship and know that nothing can possibly prevent you from getting to your destination
- Your telescope is your instrument of choice as you are always looking ahead to see what is on the horizon and how to navigate treacherous waters
- You like challenges and welcome days where activities change on a dime
- Handle and lead all aspects of a clinical research trial or trials
- Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets
- Liaise with Project Team and senior management of both Precision and sponsors, including C level
- Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
- Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
- Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
- Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
- Bachelor's degree or equivalent experience
- Proven ability to develop positive working relationships with individual and teams internally and externally
- PMs: 5+ years of clinical trial experience in pharmaceutical, biotech or CRO, including at least two (2) years in oncology
- Working understanding of GCP/ICH guidelines and the clinical development process
- Ability to drive and availability for domestic and international travel including overnight stays
- Sr PMs: 7+ years in clinical operations, data management or related discipline in CRO or pharmaceutical industry to include people management
- Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
- Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
- CRO experience
- Minimum 2+ years of experience in managing Cell Gene/ CAR-T Oncology trials
- Masters programs with concentration in a scientific or healthcare discipline
- Understanding of financial management, shown ability to identify changes in scope and successfully address those changes appropriately
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