临床研究助理
Clinical Research Associate
Precision for Medicine, Oncology and Rare Disease 不是典型的 CRO 公司。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得多的 CRA 保留率。我们现在正在招聘临床研究助理（不同职级）加入我们在德国的团队。
CRA 加入我们后，会热爱自己的工作并长期留下，因为这里有出色的人和愉快的生活质量。你将专注于平均一到两个研究项目，使你成为方案专家。出差合理，因此你的工作与生活平衡会得到改善。最重要的是——你的声音会被听到。在一家规模较小的 CRO 工作，让你在关键时刻拥有影响力和作用，并获得直接上级管理的支持。
关于你：
- 当事情不如计划进行时，你保持冷静、深思熟虑且反应迅速。
- 无论是在研究人员会议、现场访问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克服困难。
- 你对细节有极高的敏锐度。
- 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。
- 你对自己的工作质量和结果负责。
- 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机构的进展，并确保临床研究按照方案、标准操作流程、ICH-GCP 和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：确定研究人员；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：
- 本科或研究生学历，主修科学或医疗健康相关专业
- 至少一年在 CRO 或制药/生物科技行业的 CRA 经验，或同等的相关经验及能力。具有临床研究领域的站点管理或同等经验。
其他要求：
- 优秀的沟通和组织能力至关重要。团队合作精神。
- 有以客户为中心的方法的证据。
- 能够接受国内出差，包括过夜停留，出差比例可能达到约 50-60%（部分高级职位可能需要国际出差）
查看英文原文
Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. We are now recruiting Clinical Research Associates (different seniority levels) to join our team in Germany.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies 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.
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:
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
- At least one year 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.
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 German
- Experience in oncology
Preferred:
- Study start up activities experience
- CAR-T or FIH - phase III
- Medical device experience
#LI-EK1 #LI-Remote
Please, apply in English.
Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
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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 myHR@precisionmedicinegrp.com.
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