高级临床研究专员/临床研究专员II
Senior Clinical Research Associate/ Clinical Research Associate II
Precision for Medicine 不是普通的 CRO 公司。我们致力于打造良好的企业文化，并自豪地拥有远高于行业平均水平的 CRA 保留率。
CRA 加入我们后，会热爱自己的工作并长期留下，因为这里有优秀的同事和令人愉悦的生活质量。你将面对比平均数量更少的方案，帮助你成为方案专家。出差安排合理，因此你的工作与生活平衡也会得到改善。最重要的是——你的声音会被听到。在一家规模较小的 CRO 工作，让你在关键时刻能够发挥影响力并获得直接上级的有力支持。
我们正在招聘一名高级临床研究助理 / 临床研究助理 II，该职位为完全居家办公，工作地点在英国或北爱尔兰。
关于你：
- 当事情不如预期时，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，始终比别人多走一步。
- 你能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，并提出缓解措施。
- 你对自己的工作质量和结果负责。
- 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：
你将监督并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）。
资格要求：
最低要求：
- 4 年制大学学位或同等经验
其他要求：
- 候选人应 ideally 具有 CRO 或制药行业超过 1 年的 CRA 经验。
- 有肿瘤学或早期阶段经验者优先，但非必需。
- 能够接受国内差旅，包括过夜停留，差旅比例可能达到约 50-60%（某些高级职位可能需要国际差旅）
- 英语流利
Precision 的独特整合服务通过结合创新的临床试验设计，实现了精准医学的科学目标
查看英文原文
Precision for Medicine 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.
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 hiring a Senior Clinical Research Associate/ Clinical Research Associate II, this position will be fully home based working in the UK or Northern Ireland.
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:
- 4-year college degree or equivalent experience
Other Required:
- Candidates should ideally have more than 1 years CRA experience within the CRO or pharmaceutical industry.
- Oncology experience, early phase experience desirable although not essential.
- 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
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.
#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.
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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