远程工作雷达

初创公司,经理,加拿大,远程

Start -Up, Manager, Canada, remote

职能支持限定地区(需当地身份)日间重叠约 2 小时,需偶尔早起或晚睡
公司Indero
薪资未公开
工作地点Spain
地域资格限定地区(需当地身份)
时区要求日间重叠约 2 小时,需偶尔早起或晚睡
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 Spain 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
作息提示:日间重叠约 2 小时,需偶尔早起或晚睡。

职位描述
启动经理,加拿大,远程办公:
启动经理负责监督和管理多个国家临床试验站点的顺利及时启动。该职位负责所有启动活动,确保符合监管要求,并与跨职能团队合作以满足研究时间表和客户期望。理想的候选人将带来战略洞察力、运营卓越性和强大的领导力,以推动高效且高质量的站点启动。

更具体地说,启动经理职责包括:

  • 管理从头到尾的研究启动流程,包括站点选择、监管提交、站点合同和预算,以及站点启动。
  • 与项目经理和跨职能负责人协作,制定启动策略和时间表。
  • 准备并维护站点启动计划,确保选定的站点和国家优化成功研究交付的机会。
  • 主动识别并沟通影响交付的问题,并提供解决方案。
  • 监控进度是否符合这些时间表,并主动解决延迟或风险。
  • 监督并协调启动过程的每一步,以确保达成启动目标。
  • 在启动期间作为所有相关职能的主要联络人,确保有效的跨职能沟通与协作。
  • 跟踪并报告启动绩效指标,提供透明度和问责制。
  • 与项目经理合作,主导面向客户的会议,并作为启动活动与内部团队和申办方的主要联系人。

任职要求

  • 生命科学、护理或相关领域的学士学位(硕士优先)。
  • 至少3年以上临床试验启动经验,有明确的领导经验。
  • 有在矩阵式环境中管理多国启动活动和跨职能团队的证明能力。
  • 优秀的项目管理、沟通和解决问题的能力。能够在快节奏、以截止日期为导向的环境中管理多项优先任务。

我们的公司
在Indero,您将与才华横溢且积极进取的同事一起工作。我们的价值观是协作、创新、可靠和响应迅速。我们提供一个充满活力的工作环境和有吸引力的发展机会。
在此职位上,您将享有以下福利:

  • 永久全职职位
  • 灵活的工作时间
  • 带薪假期
  • 远程办公
查看英文原文

Description
Start-Up Manager, Canada, remote:
The Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities, ensures regulatory compliance, and collaborates with cross-functional teams to meet study timelines and client expectations. The ideal candidate will bring strategic insight, operational excellence, and strong leadership to drive efficient and high-quality site activation.
More specifically, the Start-Up, Manager

  • Manage the end-to-end study start-up process, including site selection, regulatory submissions, site contracting and budgeting, and site activation.
  • Define start-up strategy and timelines in collaboration with the Project Manager and cross-functional leads.
  • Prepare and maintain a site activation plan, ensuring selected sites and countries optimize opportunities for successful study delivery.
  • Proactively identify and communicate issues impacting delivery and providing proposed solutions.
  • Monitor progress against these timelines and proactively address delays or risks.
  • Oversee and coordinate each step of the start-up process to ensure activation goals are met.
  • Serve as the primary liaison among all functions involved during the start-up period, ensuring effective cross-functional communication and collaboration.
  • Track and report start-up performance metrics, providing transparency and accountability.
  • In partnership with PM, lead client-facing calls and serve as the main point of contact for start-up activities with both internal teams and Sponsors.

Requirements

  • Bachelor’s degree in Life Sciences, Nursing, or related field (Master’s preferred).
  • Minimum of 3+ years of experience in clinical trial start-up, with demonstrated leadership experience.
  • Proven ability to manage multi-country start-up activities and cross-functional teams in a matrixed environment.
  • Excellent project management, communication, and problem-solving skills. Ability to manage multiple priorities in a fast-paced, deadline-driven environment.

Our company
At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.
In this position, you will be eligible for the following perks:

  • Permanent full-time position
  • Flexible schedule
  • Vacation
  • Home-based position
  • Ongoing learning and development

About Indero
A Global Clinical Leader In Dermatology!
Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.
Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
Indero only accepts applicants who can legally work in Canada.
Originally posted on Himalayas

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