临床研究专员II/高级临床研究专员
Clinical Research Associate II/ Senior Clinical Research Associate
Precision for Medicine 不是普通的 CRO。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 留任率。
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。你将专注于平均一到两个研究,使你成为方案专家。差旅合理,你的工作与生活平衡也因此受益。最重要的是——你的声音会被听到。在较小的 CRO 工作,让你在最关键的时候有影响力和作用,并得到直接上级的支持。
Precision for Medicine 正在招聘 Clinical Research Associate II/ Senior Clinical Research Associate 加入我们在土耳其的团队。
该职位可以提供完全居家办公。
关于你:
- 当事情不如计划时,你冷静、深思熟虑且反应迅速。
- 无论是在研究者会议、现场访问还是项目组更新中,你都准备充分,总是比游戏快两步。
- 你能够快速且创造性地克服困难。
- 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、SOP、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:
- 生命科学/药学/其他健康相关学科的大学学位,或在科学或医疗保健领域具有同等经验,或为持证医疗专业人员。
- 至少两年在 CRO 或制药/生物技术行业的 CRA 经验,或同等的相关经验及/或展示出的能力。具有现场管理经验或临床研究方面的同等经验。
- 有肿瘤学监测经验。
- 有 CAR-T 经验。
其他要求:
- 优秀的沟通和组织能力至关重要。团队合作者
- 证据
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 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.
Precision for Medicine is recruiting Clinical Research Associate II/ Senior Clinical Research Associate to join our team in Turkey.
This position can be offered fully home based.
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:
- University degree life science/pharmacy/other health related discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional.
- At least 2 years of experience as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management experience or equivalent experience in clinical research
- Oncology monitoring experience.
- CAR-T experience.
Other Required:
- Excellent communication and organizational skills are essential. A team player
- Evidence of a client focused approach
- Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required.
- Ability to travel overnight. Up to 60% travel on average, based on regional requirements. International travel as needed
- Fluency in English and Turkish
Preferred:
- Start up activities experience.
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.
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.
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