Senior Clinical Project Manager
医疗精准不是你的典型 CRO.在医学精准公司,我们汇集了新技术,专业知识和运营规模,以帮助生命科学提高患者带来改变生活治疗的速度,成本和成功率。区分我们的方式是我们将临床试验执行与深入的科学知识,实验室专业知识以及先进数据科学结合在一起。我们对肿肿瘤学和罕见疾病有着强大的关注。职位总结:高级项目经理计划,指导,协调并为指定临床研究项目的活动提供服务,以确保质量,范围,成本和时间实现项目目标。总理将管理区域试验 (适度复杂性)和/或在处理复杂的全球试验中起到支持作用。下面的基本功能将描述总理在研究上扮演主要/领导总理角色时。在全球研究中的支持作用时,重要职能将由全球领导委托。工作的基本功能包括但不限于:• 为客户提供首要联系点和首要升级点;•协调并监督所有功能服务,包括外部供应商,以确定时间表和预算为基础 •管理研究预算,确保项目保持在范围内的范围内,并尽早确定任何不符合目标的活动,并根据适当情况处理。•确保功能领域充分了解研究范围,并相应地管理其功能区域的范围。•管理分配研究的财务健康,包括监督项目利能力,可收费项目的时间以及按时遵守,准确的计价和预测以支持业务目标。•制定强有力的全面项目计划,包括时间表和主动风险管理和缓解,以指导试验执行的所有参数,具有一致性和质量。•确保分配项目质量管理,包括电子技术监督机制的准备性,实施质量报告事件表格和/或纠正及预防行动计划以解决任何质量发现。•在方案交付中保持与所有功能运营的综合合作,并根据需要审查其他研究文档。•建立跟踪指标来监测试验和团队实现项目的进展。
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Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.
Position Summary:
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. The essential functions below will describe the PM acting in a primary / lead PM role on a study. When in a supportive role on a global study, the essential functions will be delegated by the Global Lead.
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 oversees 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
• Remain compliant with organisational training, time-reporting and any other administrative duties as required
• Provides on-going feedback for functional team members including annual performance reviews
• Ability to travel domestically and internationally including overnight stays
Qualifications:
Minimum Required:
• 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
Other Required:
• 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
Competencies:
• 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
We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. 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.
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
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