临床研究助理 I/临床研究助理 II
Clinical Research Associate I/ Clinical Research Associate II
Precision for Medicine 不是典型的 CRO。在 Precision for Medicine，我们整合了新技术、专业知识和运营规模，帮助生命科学领域提高将改变生命的疗法带给患者的效率、成本和成功率。我们的独特之处在于将临床试验执行与深厚的科学知识、实验室专长和先进的数据科学相结合。我们专注于肿瘤学和罕见疾病。
我们热衷于培养我们的文化，并自豪地分享比行业平均水平高出很多的 CRA 保留率。
CRA 加入我们，热爱他们的工作，并因为出色的人和愉快的生活质量而留下。你将拥有比平均数量少的方案，使你成为方案专家。差旅合理，你的工作与生活平衡也将因此受益。
最重要的是——你的声音会被听到。在一家较小的 CRO 工作，让你在关键时刻有影响力和影响力，并得到直接上级管理的支持。
我们现在正在招聘 Clinical Research Associate I / Clinical Research Associate II 加入我们在法国的团队。这是一个远程办公职位，需要前往现场进行监查访问。我们寻找位于巴黎或巴黎周边地区的候选人。
关于你：
- 当事情不如计划时，你保持冷静、深思熟虑且反应迅速。
- 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，始终领先一步。
- 你能够快速且创造性地克服困难。
- 你对细节有着无懈可击的关注。
- 你能识别潜在的研究风险，并提出如何减轻它们的解决方案。
- 你对工作的质量和结果负责。
- 你擅长通过使用经过验证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，并确保临床研究按照方案、SOP、ICH-GCP 和所有适用法规和标准进行、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）。
资格要求：
最低要求：
- 生命科学学位和/或同等经验
- 至少一年作为 CRA 的经验，无论是在哪种环境
查看英文原文
Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.
We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result.
Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
We are now recruiting Clinical Research Associate I/ Clinical Research Associate II to join our team in France. This is a remote based position with travel to sites for monitoring visits. We are looking for candidates based in Paris or Paris area.
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.).
Qualifications:
Minimum Required:
- Life science degree and / or equivalent experience
- 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research.
- Experience managing oncology studies
- Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)
Other Required:
- Excellent communication and organizational skills are essential. A team player.
- Evidence of a client focused approach
- 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 for non-English speaking countries the local language of country where position based
Preferred:
Study start up activities experience.
Please apply in English.
#LI-EK1 #LI-Remote
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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.
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