远程工作雷达

临床项目经理 / 资深临床项目经理

Clinical Project Manager / Senior Clinical Project Manager

职能支持限定地区(需当地身份)
公司precisionmedicinegroup
薪资未公开
工作地点Remote, Poland
地域资格限定地区(需当地身份)
时区要求无特别要求
用工类型未标注
发布时间2026-07-13
数据来源Greenhouse
前往企业招聘页投递 →
注意地域限制:该职位明确限定在 Remote, Poland 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。

你是否是一位在临床试验领域有经验的全职能项目经理,正在应对肿瘤学中新型化合物研发面临的挑战?你是否热衷于影响全球患者健康和生命?你是否采用咨询式的方法进行试验管理,成为试验运营交付中的宝贵合作伙伴?

Precision for Medicine 正在寻找一位具有肿瘤学经验的临床项目经理/高级临床项目经理,有在 CRO 环境中管理全职能临床试验的经验,加入我们的全球团队。

在这个关键职位中,你将对肿瘤学领域的全球/区域(I-IV期)临床试验项目进行全面管理。负责临床项目的交付,所有职能部门的监督,并确保达成的时间表、范围、成本和质量。

参与所有研究阶段,包括提案策略、开发、成本核算和投标辩护,并全程跟进研究直至完成,管理客户关系、项目团队和预算及时间表。

你将与内部和外部利益相关者组成的跨职能团队合作,推动质量并协调研究团队。

我们提供一个充满活力、专注、协作的团队,成员喜欢接受挑战,在细节中茁壮成长,并在动态环境中蓬勃发展。如果你不惧承担责任,寻求积极的团队合作以实现卓越的工作成果,我们有适合你的机会。

我们将如何让你忙碌并支持你的成长:

  • 你将根据研究预算和工作范围独立领导临床项目。你将运用强大的人际交往和组织能力,设定并实现项目的执行目标;包括合同目标和财务目标。你可能需要负责国际试验。
  • 作为客户的主要联络人,提供优质的客户服务,包括参与提案活动和客户演示
  • 与 Precision 和赞助商的项目团队及高级管理层(包括高管)进行沟通
  • 处理并领导所有临床研究试验或试验的各个方面
  • 对所有职能领域(包括数据管理、安全、临床、医学监测和生物统计学等)进行整体项目管理
  • 为客户提供项目状态更新
查看英文原文

Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?

Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our global team.

In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology.  Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.

Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.

You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team.

We offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.

How we will keep you busy and support your growth:

  • You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well.
  • Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
  • Liaise with Project Team and senior management of both Precision and sponsors, including C level
  • Handle and lead all aspects of a clinical research trial or trials
  • Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
  • Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
  • Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
  • Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets

Requirements:

  • Degree or similar related life science qualification, or equivalent combination of education and experience.
  • Previous experience in a full service/global Project Management role working in the CRO industry is essential.
  • Extensive experience working within Clinical Operations position within a CRO, and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
  • Experience managing studies within Oncology
  • Working understanding of GCP/ICH guidelines and the clinical development process
  • Ability to drive and availability for domestic and international travel including overnight stays
  • Be able to communicate effectively in the English language both written and spoken
  • Strong presentation skills
  • Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
  • Proven ability to develop positive working relationships with individual and teams internally and externally
  • Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan

Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

We are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development.

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.

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

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.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

本页面信息整理自 Greenhouse,版权归原发布方所有。职位可能随时关闭,投递请以原始页面为准。 本站只做信息聚合展示,不参与招聘流程,也不向求职者收取任何费用。

该公司其他在招职位

站点启动总监

precisionmedicinegroupRemote, Australia; Remote, China; Remote, 2026-08-14
其他明确接受中国求职者

初创企业负责人 APAC

precisionmedicinegroupRemote, Australia; Remote, China; Remote, 2026-04-10
其他明确接受中国求职者

← 返回全部职位