Clinical Project Manager-Neurology
- Canada
Full-time
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Job details
- Job type
- Full-time
- Posting language
- English
- Posted
Original job description
Job Purpose:
To draft and implement project management effectively, and clinical operation conducting for related projects to ensure that clinical research affairs works smoothly.
Responsibilities:
- Acts as the primary liaison for the sponsors of the responsible studies.
- Leads and directs cross functional team leaders and third parties/vendors.
- Manages project contractual deliverables in terms of project milestone payments and qualify insurance.
- Manages project scopes and project costs timely to ensure control of project financial risk.
- Ensures adherence to company SOP, policies and guidelines at the project level.
- Ensures projects comply with Tigermed processes and systems such as CTMS, OA eTMF etc., including escalation to relevant functional and operational management.
- Proactively attends bid defense process.
- Perform necessary training for Project team colleague and build the effective team;
- Provides feedback on project team member’s performance to respective line managers.
Qualifications:
- Bachelor degree or above in Medical, Pharmacology or Biology related major. College diploma can be accepted if the personal attributes and relevant project management experience are sufficiently justified.
- Adequate knowledge of current drug development processes and regulations, including local regulations, GCP, clinical trial operations. Current GCP certificate required Business skills such as budgeting and business knowledge are a bonus.
- Solid neurology therapeutic‑area project management experience is required; AIS (Acute Ischemic Stroke) study experience is highly preferred.
- A minimum of 10 years’ industry experience, including a minimum of 6 years’ project management experience, CRO work experience preferred. If outstanding PM achievement is shown, suitable candidate will be considered.
- Fluent in both written and spoken English; Local languages fluency is preferred.
- Excellent command of Microsoft offices.
- Strong project management skill; Strong time management skill.
More about this job
Responsibilities
Lead clinical research projects by serving as the primary sponsor liaison and directing cross-functional teams and vendors. Manage project scope, costs, contractual deliverables, compliance, systems, team training, and performance feedback.
Requirements
Requires at least 10 years of industry experience, including at least 6 years in project management, with solid neurology project management experience; acute ischemic stroke experience is highly preferred. Requires a relevant medical, pharmacology, or biology degree (with a diploma potentially accepted based on experience), current GCP certification, knowledge of drug development and clinical trial regulations, and fluent written and spoken English.
Skills
- Project Management
- Clinical Operations
- Neurology
- Clinical Trial Operations
- Good Clinical Practice
- Drug Development
- Budgeting
- Financial Risk Management
- Contract Management
- Stakeholder Management
- Cross-Functional Leadership
- Vendor Management
- Team Training
- Time Management
- Microsoft Office
- English Communication
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Management & Leadership
- Science & Research
Keywords
- Clinical Project Management
- Neurology
- Clinical Operations
- Clinical Research
- Acute Ischemic Stroke
- Drug Development
- Clinical Trial Operations
- Good Clinical Practice
- GCP Certificate
- Local Regulations
- Project Milestones
- Milestone Payments
- Project Contractual Deliverables
- Project Scope Management
- Project Cost Management
- Financial Risk
- Standard Operating Procedures
- CTMS
- OA eTMF
- Bid Defense
- Cross-Functional Teams
- Vendor Management
- Project Budgeting
- Team Training
- Microsoft Office
- CRO
- Pharmaceutical Manufacturing