助理项目经理 - 肿瘤学（美国/加拿大）
Associate Project Manager - Oncology (US/Canada)
我们是谁
我们是一家全球性的中型CRO，不断突破界限、创新和发明，因为治愈世界上最顽固疾病的道路不是由那些安于现状的人铺就的。它是由那些采取开创性、创造性方法并以质量和卓越来实施的人所打造的。
我们是Worldwide Clinical Trials，我们是一个由3500多名专家、有远见的思考者、梦想家和实干家组成的全球团队，我们正以最好的方式改变世界对CRO的认知。
我们的使命是每天以热情和目标感工作，改善人们的生活，我们正在寻找同样重视这一追求的人。
为什么选择Worldwide
我们认为每个人都在为患者及其护理者带来巨大影响方面发挥着重要作用。从我们亲力亲为、平易近人的领导，到我们紧密协作、互相支持的团队，我们致力于让来自不同背景和经验的专业人士取得成功。我们优先打造一个多元且包容的环境，持续促进协作与创造力。我们自豪地成为这样一个职场，在这里，人们可以做真实的自己，并每天被激励去完成最出色的工作。加入我们吧！
Worldwide的项目管理做什么
Worldwide Clinical Trials的项目管理完美结合了运营严谨性和治疗专业知识，采用以客户为中心的方法。我们的全球项目负责人（GPLs）和临床项目经理（CPMs）专业地引导项目团队，确保高质量交付，专注于“第一次就把事情做对”。
项目管理团队参与试验的所有方面，与科学和治疗领导合作，协调跨项目团队，并提供灵活、创新和主动的解决方案。在Worldwide，您将专注于特定的治疗领域，这不仅为您提供深入了解全球运营专业知识的机会，还能从我们专家带来的卓越科学和医学背景中受益。
您将负责
- 负责从启动到结束的临床试验的整体协调和管理工作。
- 定义和管理项目资源需求，并为关键资源制定应急计划。
- 确保所负责项目的计划设计、实施、跟踪和修订顺利进行。
- 保证所有项目交付物满足客户的时效/质量/成本期望。
- 达成财务目标
查看英文原文
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What Project Management does at Worldwide
Worldwide Clinical Trials Project management is the perfect blend of operational rigor and therapeutic expertise, with a client-focused approach. Our Global Project Leads (GPLs) and Clinical Project Managers (CPMs) expertly guide our project teams to deliver with high quality, focusing on “doing it right the first time”.
The Project Management team is engaged in all aspects of the trial collaborating with scientific and therapeutic leadership, coordinating across project teams, and providing flexible, innovative, and proactive solutions. At Worldwide, you will be dedicated to a specific therapeutic area which will not only give you an opportunity to develop in-depth global operational expertise, but also benefit from exceptional scientific and medical background that our experts bring.
What you will do
- Be responsible for the overall coordination and management of clinical trials from start up through close out activities.
- Define and manage project resource needs and establish contingency plans for key resources.
- Ensure successful design, implementation, tracking and revision of project plans for assigned projects.
- Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations.
- Meet financial performance targets for the assigned clinical projects.
- Can be key client contact for assigned projects.
What you will bring to the role
- Excellent oral and written communication skills, ability to chair meetings and participate in bid defenses.
- Excellent planning and organizational skills with effective time management.
- Excellent interpersonal skills.
- Ability to work logically and methodically.
- Initiative and problem-solving skills.
- Ability to negotiate and liaise with clients in a professional manner.
Your experience
- University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
- Minimum of three (3) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks.
- In lieu of the above requirements, candidates with > three (3) years supervisory experience in a health care setting and two (2) years clinical research experience in the pharmaceutical or CRO industries will be considered and/or proven ability and demonstration of relevant experience and skill in clinical development.
- Experience working with Oncology studies is required for this role.
- Ability to travel when needed.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
Originally posted on Himalayas