内部临床研究助理I - 保加利亚 - 远程
In-House Clinical Research Associate I - Bulgaria - Remote
职位名称：内部临床研究助理 I - 保加利亚 - 远程
工作地点：保加利亚索菲亚
工作地点类型：远程
工作合同类型：全职
职位级别：初级
我们是谁
我们是一家全球中型CRO，不断突破界限、创新和发明，因为解决世界上最顽固疾病治愈之路，不是由那些安于现状的人铺就的，而是由那些采取开创性、创造性方法并以质量和卓越加以实施的人所构建的。
我们是Worldwide Clinical Trials，我们是一个由3500多名专家、有远见的人、梦想家和实干家组成的全球团队，我们一起正在以最好的方式改变世界对CRO的看法。
我们的使命是每天以热情和目标感工作，改善人们的生活，我们正在寻找同样重视这一追求的人。
为什么选择Worldwide
我们认为每个人都在为患者及其护理者带来巨大影响方面发挥着重要作用。从我们亲力亲为、易于接触的领导，到我们紧密协作、互相支持的团队，我们致力于让来自不同背景和经验的专业人士取得成功。我们优先打造一个多元且包容的环境，持续促进合作与创造力。我们自豪地成为这样一个职场，在这里，人们可以做真实的自己，并被激励每天做出最好的工作。加入我们吧！
在Worldwide，临床运营现场管理做什么
开启一段充实的临床运营职业生涯，对患者的生活产生持久的影响。加入Worldwide Clinical Trials，体验无与伦比的CRO经验，你可以推动非凡的科学突破，并为每个成功的临床试验的核心做出贡献。
与各个治疗领域的杰出人才一起工作，你将有机会与来自不同背景和专业领域的顶级同事密切合作。我们致力于推进临床研究，在支持性、团队导向的氛围中，我们的亲力亲为的领导和敬业的团队成员共同努力，为我们的客户创新并解决复杂挑战。
你将负责
- 确保从研究现场提交的数据质量，并确保数据及时提交，包括所有安全事件的适当报告和跟进
- 确保监管文件和伦理提交文件的完整性和汇编，根据需要和要求进行（例如IRB批准、知情同意）
查看英文原文
Job Title: In-House Clinical Research Associate I - Bulgaria - Remote
Job Location: Sofia, Bulgaria
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What Clinical Operations Site Management does at Worldwide
Embark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives. Join Worldwide Clinical Trials for an unparalleled CRO experienced, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial.
Working alongside brilliant minds across a variety of therapeutic areas, you will have the chance to collaborate closely with top-tier colleagues from diverse backgrounds and specialties. Our commitment to advancing clinical research is cultivated in a supportive, team-oriented atmosphere, with our hands-on leadership and dedicated team members working together to innovate and solve complex challenges for our customers.
What you will do
- Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
- Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)
- Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
- Perform feasibility studies/site identification activities for potential sites, as requested
What you will bring to the role
- Excellent interpersonal, oral, and written communication skills
- Ability to contribute to a team remotely
- Strong customer focus, ability to interact professionally with a sponsor contact
- Proficiency in Microsoft Office, CTMS, and EDC Systems
Your background
- Four-year college curriculum with a major concentration in life science preferred but not required, OR
- Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant
- Proficiency in English,Bulgarian and one other language ( German, French, Italian, Spanish )
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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Originally posted on Himalayas