高级临床试验经理(CTM)
Senior Clinical Trial Manager (CTM)
Senior临床试验经理(CTM)
地点:该职位可远程工作,根据需要可能需前往波士顿地区。
职位概述
该职位将负责在国内和国际临床研究的启动、执行和结束阶段的项目管理,包括研究概念和设计、可行性评估、研究启动、合同和预算监督、数据交换以及数据分析和解释的支持。
该职位需要具备在既定临床试验范式中工作的知识和经验,同时探索并接受新的研究方法,以支持数据聚合和分析,从而推进患者护理。高级CTM将参与临床项目团队,以成本效益和及时的方式实现高质量成果。其将是建立临床团队关键实践和流程的关键团队成员。
主要职责
- 管理从方案概念到临床研究报告的临床试验成功执行,遵守良好临床实践(GCP)指南和国际法规
- 与关键合作者进行战略协作
- 建立并监督临床试验相关的跟踪工具,如监管文件、试验主文件(TMF)、启动进度、筛选/入组、研究发票/付款、项目预算等
- 作为关键成员参与IRB/EC和监管提交
- 监督TMF审查,确保完整性和检查准备就绪
- 定期审查文件,确保符合临床运营和/或项目特定的质量要求(例如SOP、工作实践、培训指南)
- 识别并缓解研究风险,必要时进行升级
- 指导举措,以识别并实施临床开发中的最佳实践和持续改进计划
- 教育和专业经验
- 需要科学领域的学士学位;具有高级科学学位者优先
- 在发起方或CRO环境中直接管理临床试验5年以上
- 深入了解临床试验运营、ICH、GCP指南及其他适用的监管要求
- 有指导临床运营团队成员的经验
- 有在跨多个职能领域(如质量保证、数据管理、生物统计、医学写作、安全、临床供应、财务)团队工作的经验
- 其他必备条件和关键成功因素
- 具有求知欲、创新精神和创造性解决问题的能力,具有电子健康记录系统(EHR)和数据整合经验者优先
查看英文原文
Senior Clinical Trial Manager (CTM)
Location: This position may be performed remotely with travel to the Boston area as needed.
Position Summary
This role will be responsible for project management in the initiation, execution and close out of domestic and international clinical studies, including study concept and design, feasibility assessments, study start-up, contract and budget oversight, data exchange and support of data analysis and interpretation.
This position requires both the knowledge and experience to work within established clinical trial paradigms while exploring and embracing new approaches to conducting research to support data aggregation and analysis to advance patient care. The Sr. CTM will participate on clinical project teams to achieve quality results in a cost-effective and timely manner. S/he will be a key team member to establish key practices and procedures for the clinical team.
Primary Responsibilities
- Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international regulations
- Manage strategic engagement with key collaborators
- Set-up and oversee clinical trial-related trackers such as regulatory documents, trial master file (TMF), startup progress, screening/enrollment, study invoices/payments, project budgets, etc.
- Key contributor to IRB/EC and regulatory submissions
- Oversee TMF reviews to ensure completeness and inspection readiness
- Regularly review documents to ensure adherence to Clinical Operations and/or project specific quality requirements (e.g. SOPs, work practices, training guides)
- Identify and mitigate against study risks, escalating as necessary
- Direct initiatives to identify and implement best practices and continuous improvement plans in clinical development
Education and Professional Experience
- Bachelor’s degree in a scientific field required; advanced scientific degree a plus
- 5+ years directly managing clinical trials in Sponsor or CRO setting
- In-depth knowledge of clinical trial operations, ICH, GCP Guidelines and other applicable regulatory requirements
- Experience directing members of clinical operations teams
- Experience working in a team across multiple functional areas (e.g., Quality Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance)
Other Essentials and Key Success Factors
- Intellectual curiosity, innovation and creative problem solving with an entrepreneurial spirit
- Ability to think critically in fast-paced projects with a keen sense of urgency and demonstrated ability to problem solve
- Self-motivated and able to work autonomously, as well as a member of a collaborative team
- Highly-organized and detail-oriented with a passion to deliver quality results
- Strong verbal and written communication skills with an ability to build relationships internally and externally
- Highest levels of professionalism, confidence, personal values and ethical standards
Annualized Base Salary
$168,000—$188,000 USD
Compensation & Benefits
At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long-term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let’s achieve the impossible together!
Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
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