Clinical Project Manager
Precision For Medicine
full-time
Posted on:
Location Type: Remote
Location: Singapore
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About the role
- The Senior/Project Manager plans, directs, coordinates, and delivers activities for designated clinical-study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.
- PM will either manage regional trials (moderate complexity) and/or supportive role in managing complex global trials.
- Serve as primary point-of-contact and primary escalation point to the client.
- Coordinate and oversee all functional services including external vendors to the established timeline and budget.
- Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate.
- Ensure functional areas are fully aware of the study scope and are managing the scope for their functional areas accordingly.
- Manage the financial health of assigned studies, including oversight of the project profitability, billable project hours, and compliance with on time, accurate billing and forecasting to support business objectives.
- Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality.
- Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings.
- Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation.
- Establish tracking metrics to monitor trial and team progress towards project goals.
- Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise.
- Lead both internal and client meetings and set expectations for the project team.
- Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues.
- Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project.
- Support business development and marketing activities as appropriate, including travel to Bid Defence meetings as required.
- Perform other duties as assigned by management.
Requirements
- Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred
- Minimum of 3-7 years of clinical research experience or proven competencies for this position and a minimum of 2-4 years of leading a project
- Experience managing regional trials (moderate complexity) and/or supportive role in managing complex global trials
- Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS
- Good communication and interpersonal skills to effectively interface with others in a team setting
- Good organizational skills, attention to detail, and a customer service demeanor
Benefits
- Paid time off
- Professional development opportunities
- Health insurance
- Retirement plans
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchproject managementbudget managementrisk managementquality managementstudy designdata analysisperformance monitoringprotocol compliancetraining implementation
Soft Skills
communicationinterpersonal skillsorganizational skillsattention to detailcustomer serviceleadershipproblem-solvingteam collaborationclient managementreporting
Certifications
degree in sciencedegree in health-related fieldadvanced degree (preferred)