临床研究专员II
Clinical Research Associate II
Precision for Medicine 不是普通的 CRO。在 Precision for Medicine，我们整合了新技术、专业知识和运营规模，帮助生命科学领域加快新疗法的开发速度，降低费用并提高成功率。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病领域。
我们热衷于培养企业文化，并自豪地分享比行业平均水平更高的 CRA 保留率。CRA 加入我们后，会爱上这份工作并长期留下，因为这里有优秀的同事和愉快的生活质量。你将负责的方案数量低于平均值，这有助于你成为方案专家。出差合理，工作与生活平衡也会因此受益。最重要的是，你的声音会被听到。在一家较小的 CRO 工作，让你在关键时刻拥有影响力和作用，并得到直接上级的有力支持。
我们现在正在招聘 Clinical Research Associate II 加入我们在荷兰的团队。这是一个远程办公岗位，需要前往现场进行早晨访视。我们寻找在荷兰的候选人，有生物制药监查经验。
关于你：
- 当事情不如预期时，你冷静、深思熟虑且反应迅速。
- 无论是在研究者会议、现场访视还是项目团队更新中，你都准备充分，总是比别人多走一步。
- 你能够快速而创造性地解决困难。
- 你对细节有着极高的敏锐度。
- 你能识别潜在的研究风险，并提出缓解措施。
- 你对工作的质量和结果负责。
- 你擅长通过成熟有效的解决策略处理冲突。
- 我们会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、标准操作规程、ICH-GCP 和所有适用法规和标准进行。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视等）。
- 资格要求：
- 最低要求：
- 生命科学学位或同等经验
- 在 CRO 或相关领域担任 CRA 至少 2 年
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 II to join our team in the Netherlands. This is a remote based position with travel to sites for morning visits. We are looking for candidates in the Netherlands with biopharma monitoring experience.
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
- 2 years 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.
- 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, Dutch
- French will be a plus
- oncology monitoring experience will be a plus
Preferred:
· Study start up activities experience.
Please apply in English.
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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.
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