全球专业参与协调员 / 高级项目专员（医学）
Global Professional Engagement Coordinator / Senior Project Specialist (Medical
当我们的价值观一致时，我们能够实现无限可能。
在Parexel，我们都有相同的目标——改善全球健康。从临床试验到监管、咨询和市场准入，我们提供的每项临床开发解决方案都建立在一个特别的基础之上——对所做工作的深刻信念。
无论我们在Parexel做什么，都在为最终能造福患者的疗法做出贡献。我们认真对待工作，以同理心去做，并致力于带来改变。
在Parexel FSP，你将加入一个拥有丰富经验和知识的团队。
我们寻找像你这样主动做事、更聪明的人，以及希望在个人和职业上成长的人。
我们认可并坚持所有人的价值，我们做事的方式，我们对创新的追求，最重要的是我们的患者。
我们正在寻找一名全球专业参与协调员（高级项目专家），100%远程办公，位于罗马尼亚。
专注于客户。
你的职责包括
• 负责在CSA下完成科学领袖合规参与所需的所有文件。
• 使用内部流程、模板和系统提交以获得所有必要的批准。
• 使用公司文档库维护CSA所需的所有文件。
• 向请求业务部门提供所有必要信息，并向科学领袖传达行政细节。
• 协调科学领袖和外部供应商以管理物流。
• 与EMEAC GMAC GEIME团队对接，获取输入和医学教育会议所需的行政支持。
• 对参与活动规划和执行的供应商/机构进行监督。
• 负责确保指定系统和数据仓库符合内部政策和合规指标。
我们期望你具备
• 至少3-5年在医药行业从事医学事务和合规的行政支持经验，以及科学/医学领袖会议管理经验（担任医学专员或类似职位）——不要求临床试验背景，但必须有医学事务/KOL参与经验。
• 了解合同流程。
• 英语书面和口头沟通能力强，具备项目管理能力，了解行业合规规则和要求。
• 在管理医学/科学领袖参与和会议方面具有专业知识
查看英文原文
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
At Parexel FSP, you will be joining a team with a wide variety of experiences and knowledge.
We’re looking for people like you to take the initiative to do things better and smarter people who want to grow personally and professionally.
We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.
We are looking for a Global Professional Engagement Coordinator (Senior Project Specialist) 100% home based in Romania.
Sponsor dedicated.
Your tasks will be
• Responsible for finalizing all required documentation for a compliant engagement of scientific leader under CSAs.
• Uses internal processes, templates, and system for submission to obtain all required approvals.
• Uses company document repository to maintain all required documentation for CSAs.
• Provides all necessary information to requesting business area and communicates the administrative details to the scientific leader.
• Aligns scientific leader and external vendor to manage logistic.
• Align with EMEAC GMAC GEIME team for administrative support needed in Input and Medical Education meetings.
• Provides oversight to vendor/agencies involved in the planning and execution of activity.
• Accountable for ensuring that assigned system and data repository complies with internal policy and compliance metrics.
From you we expect:
• Minimum 3 - 5 years' experience in administrative support to medical affairs and compliance, scientific / medical leader meeting management in pharma (being Medical Associate or similar) - not background clinical trials-focused but medical affairs/KOL engagement is a must.
• Contracting process knowledge.
• Strong written and verbal communication skills in English, demonstrated project management skills, and compliance knowledge including knowledge of industry compliance rules and requirements.
• Expertise in managing medical/scientific leader engagements and meetings is required.
• Experience using Veeva Vault
• Education required: BA/BS in science, business, administration, healthcare, or related field.
• The ability to travel (intermittent 10 - 20%).
We will offer you
- Premium salary.
- Attractive benefits.
- Medical care plan: Health, Dental & Vision.
- Life Assurance.
- Excellent work environment.
- Culture of teamwork and collaboration.
- People who motivate and face challenges together.
- Innovative technology.
- Excellent training.
Join a global community where you can transform your career into a life-changing achievement.
Apply directly or contact us via email at
Originally posted on Himalayas