Principal Project Data Manager (Canada)
at Allucent
Toronto, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Dec, 2024 | USD 94088 Annual | 02 Oct, 2024 | N/A | Good communication skills | No | No |
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Description:
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Principal Project Data Manager (PrPDM) to join our A-team (hybrid*/remote). As a PrPDM at Allucent, you are responsible for leading, coordinating and overseeing data management activities, timelines and project finances of the Allucent Data Management (DM) department.
This position manages and coordinates DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meets the quality standards and regulatory requirements for analysis and reporting.
This position takes responsibility for the overall coordination and management of Biometrics standalone projects, large and complex trials, global programs and/or multiple projects belonging to one client.
This position also provides leadership and is a Subject Matter Expert (SME) in relevant data management areas and leads cross-functional initiatives, including the development of departmental processes, tools, and training of staff.
The PrPDM is a member of the Data Management staff.
Responsibilities:
- Lead and serve as primary contact for DM with all relevant parties both internally (e.g. Biostatistics and if applicable other functional groups, such as Project Management, Clinical Operations) and externally (e.g. sponsors, vendors (EDC, external data), investigational sites)
- Provide expert input in improving processes and deliverables that will support improved client relationships.
- Actively monitor for Data Management developments and clinical research related regulations and share this with DM Directors and team members
As a Project Manager for Biometrics stand-alone studies, the Principal Project Data Manager will:
- Lead and coordinate the Biometrics project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract, with minimal supervision from Line Manager
- Create and execute project management plans required for project delivery and in accordance with established processes
- Establish requirements for and ensures project-specific training plan for internal team members
- Establish clear communication lines and escalation pathways, communicate with project stakeholders, both internally (e.g. Clinical Programmers, Data Scientists, Biostatistics and other functional groups) and externally (e.g. sponsors, vendors (EDC, external data) and other external parties)
- Establishes requirements for and ensures project-specific training plan for internal team members
- Establish project risk management plan with input from client and functional stakeholders and oversee adherence and updates throughout the project lifecycle
- Lead internal meetings with internal team members and external meetings with sponsor, and third party (data) vendors, including Kick Off Meetings (KOM) and Investigator Meetings based on project scope
- Provide support for vendor identification, qualification and selection and manage vendors
- Manage vendors and vendor relationships as required for project delivery
- Arrange, maintain and circulate project progress and status reports
As a Project Manager for Biometrics stand-alone studies and/or large, complex or multiple studies with same client, the Principal Project Data Manager will:
- Lead the Biometrics project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract
- Ensure overall consistency across all client studies within a set of projects; this especially relates to the DM activities; Data Management Plan (DMP), CRF design, data cleaning and query management) and for Biometrics stand-alone projects also includes statistical deliverables (SAP, TLFs)
- Lead internal meetings with internal project team members. Support and participate in external meetings with sponsor, including Kick Off Meetings (KOM) and Investigator Meetings based on project scope
- Interact, negotiate and influence internal and external team members in a professional manner and with successful outcomes
- Ensure effective and efficient resource utilization across projects and programs
- Manage the study budget, evaluate financial project health and manage monthly status updates for invoicing. Participate in monthly project review meetings
- Proactively recognize and address any changes in scope. Liaise to execute contract amendments
- Oversee Sponsor relationships
- Assist in contracts negotiation and contracting process with vendors (EDC, IRT, eCOA)
- May support operational Data Management activities, also to ensure and assess quality
- Oversee and ensure the Trial Master File for DM services in scope is kept up to date and audit/inspection ready.
- Contribute to other areas of business as required
- Research, propose and lead initiatives for improving efficiency
Management, Learning, & Development
- Actively support to staff learning & development within the company
- Share relevant information at applicable DM departmental meetings and organize and lead DM-related meetings and discussions
- Represent the company through active participation at professional meetings, webinars or seminars
- Provide leadership, training, guidance and coordinate Data Management training for relevant staff. Support in development of new training material
- Mentors and trains new Project Data Managers
- Participate in the interview process for new recruits
- Proactively track Data Management related regulatory development trends and updates, in consultation with department Global Head and/or Senior Directors, for further alignment and improvement of current processes
- Contribute to other areas of business as required
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
IT Software - Other
Clinical Pharmacy
Graduate
Proficient
1
Toronto, ON, Canada