[Hiring] Senior Clinical Project Manager/Clinical Project Manager @Precision for Medicine

Role Description

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. The PM will either manage regional trials (moderate complexity) and/or serve in a supportive role in managing complex global trials. The essential functions of the job include but are not limited to:

• 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 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 implement 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.
• Remain compliant with organisational training, time-reporting and any other administrative duties as required.
• Provide ongoing feedback for functional team members including annual performance reviews.
• Ability to travel domestically and internationally including overnight stays.

Qualifications

• Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred.
• Minimum of 4-7 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.
• Mandarin Speaking as this is required to cover East Asia market.

Requirements

• Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as well as the ability to implement such items.
• Working knowledge of project management techniques and tools.
• Experience working in a cross-functional project management environment.
• Fundamental understanding of cross-functional management.
• Fundamental understanding of project planning, risk management and change management with an awareness of appropriate escalation.
• High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective.
• Ability to lead and inspire excellence within a study team.
• Ability to create an environment where study team members have a sense of ownership that will lead to increases in productivity and efficiency.
• Results oriented, accountable, motivated and flexible.
• Good time management, negotiation, critical thinking, decision making, analytical and interpersonal skills.
• Good presentation, verbal and written communications skills.
• Fundamental understanding of project management software.
• Experience in pharmaceutical and/or device research required.

Benefits

• We strive to ensure employees feel appreciated for the contributions they make every single day.
• You will provide input and have your ideas valued and nurtured, impacting positive change for the company.