Clinical Project Manager-Neurology

Job summary

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.

Job details

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.

What you’ll do

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.

Listed skills

• Clinical Operations · Preferred
• Time management · Preferred
• Budgeting · Preferred
• Microsoft Office · Preferred
• Project management · Preferred
• Stakeholder Management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• 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

Job areas

• Healthcare
• Management & Leadership
• Science & Research