高级临床研究专员
Senior Clinical Research Associate
在Precision for Medicine，我们始终致力于与优秀人才建立联系，目前我们正在寻找波兰、匈牙利、英国、法国和德国的高级临床研究助理，以支持一个专门的FSP合作项目，在高度协作且注重质量的环境中与战略赞助方紧密合作。
这份长期有效的职位信息是我们的持续人才管道策略的一部分，使有兴趣的候选人能够被考虑进入未来与新项目需求相匹配的机会。虽然目前可能没有立即的空缺，但符合我们预期需求的候选人将在有合适机会时被优先考虑。
该职位可在波兰全职居家办公。
关于你：
- 事情不如计划时，你冷静、善于思考且反应迅速。
- 无论是在研究者会议、现场访问还是项目团队更新中，你总是准备充分，始终保持领先一步。
- 你能够快速而创造性地克服困难。
- 你对细节有着极高的敏锐度。
- 你能识别潜在的研究风险，并提出如何减轻这些风险的解决方案。
- 你对工作的质量和结果负责。
- 你擅长通过使用成熟有效的解决策略来处理冲突。
我们将如何让你忙碌并支持你的成长：
你将监督和负责临床研究在研究现场的进展，确保临床研究按照方案、SOP、ICH-GCP以及所有适用的法规和标准进行、记录和报告。你将协调设置和监控研究所需的所有必要活动（例如：确定研究者；协助准备监管提交文件，进行研究前和启动访问等）。
高级临床研究助理负责适当规模的临床试验，并为范围更大的临床研究团队提供支持。你还将有机会培训和指导初级员工。你将直接与客户互动，发起付款，并参与提案活动，包括开发和客户演示。
资格要求：
最低要求：
- 4年制大学学位或同等经验
- 持有临床研究助理证书
其他要求：
- 在CRO、制药、生物技术或医疗设备环境中至少5年的CRA/SCRA经验
- 在多种治疗领域进行临床试验的监控经验
查看英文原文
At Precision for Medicine, we are always looking to connect with exceptional talents, and we are currently seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to support a dedicated FSP partnership, working closely with a strategic sponsor in a highly collaborative and quality-focused environment.
This evergreen posting is part of our ongoing talent pipeline strategy and enables interested candidates to be considered for future opportunities aligned with upcoming project requirements. While there may not be an immediate opening, candidates whose experience matches our anticipated needs will be considered for future opportunities as they arise.
This position can be offered fully home-based within the United Kingdom.
About you:
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
- You take responsibility in the quality and outcomes of your work.
- You are adept at handling conflict by using tried and true resolution strategies.
How we will keep you busy and support your growth:
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Senior CRAs handle appropriately sized clinical trials, and support clinical study teams with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Qualifications:
Minimum Required:
- 4-year college degree or equivalent experience
- Holder of CRA certificate
Other Required:
- Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
- Experience monitoring clinical trials across a variety of therapeutic areas.
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Fluency in English and the local language is required
- Additional language(s) will be considered an asset
Preferred:
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
- Study start up activities experience
- For Senior CRAs, understanding of financial management
Why Precision for Medicine?
At Precision for Medicine, we combine the agility and collaboration of a specialized CRO with the scientific expertise needed to support innovative clinical development programmes. Our employees are empowered to make an impact, build meaningful client relationships, and grow their careers in an environment that values quality, accountability, and professional development.
Please note: This is an evergreen opportunity intended to build our network of experienced clinical research professionals for future project requirements. Hiring decisions and timelines will be dependent upon business needs and upcoming study opportunities.
Please, apply in English.
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 .
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 so we can investigate and take appropriate action.
Originally posted on Himalayas