← 返回岗位列表美国专业服务fulltime

临床科学家 - 肿瘤学 - 美国任意地点居家办公 - FSP

雇主

Parexel

地点

远程 · Remote · 美国

待遇

$面议

工作模式

远程

截止日期

1月4日

🤖 AI 简历匹配评估

检测你的简历与该岗位的匹配度,免费

免费评估

岗位摘要

When our values align, there's no limit to what we can achieve.

岗位职责

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Job Purpose:
The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management).
Key Accountabilities:
May include but not limited to the following:
Clinical Trial OperationalDelivery
• May support a single study or multiple studies
• May lead a study with limited scope (e.g., Survival Follow-up)
• Liaises with cross-functional lines as appropriate
• May interact with internal and external stakeholders (study sites,
committees, etc.) in support of clinical study objectives
Compliance with Parexel Standards
• Complies with required training curriculum
• Completes timesheets accurately as required
• Submits expense reports as required
• Updates CV as required
Maintains a working knowledge of and complies with Parexel processes,
ICH-GCPs and other applicable requirements
Skills:
• Demonstrated oral and written communication skills
• MS Office Suite Experience Required– including Word, Excel, and Power Point
Advanced Excel skills required (pivot tables, v-lookups)
• Proficient in written and spoken English
• Willingness to travel as required for key company meetings
Knowledge and Experience:
• Pharmaceutical experience beneficial but not required
• Oncology experience is required
2 years medical monitoring experience preferred
Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management
Education:
• Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
• If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years)
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Originally posted on Himalayas

申请条件

- 具备良好的口头和书面沟通能力
- 熟练使用MS Office套件,包括Word、Excel和PowerPoint
- 具备高级Excel技能(数据透视表、VLOOKUP)
- 精通英语书面和口语
- 愿意根据公司关键会议需要出差
- 具有制药行业经验者优先,但非必需
- 必须具备肿瘤学经验
- 优先考虑2年医学监查经验

雇主简介

Parexel is a global clinical research organization (CRO) that provides clinical trial and research services to pharmaceutical and biotech companies, including early-phase clinical studies.

对这个岗位感兴趣?

上传简历,AI 免费评估匹配度,一键发送至雇主

无需注册,上传简历即可投递

申请海外岗位,英文简历符合当地格式规范吗?

AI 自动评估你与该岗位的匹配度,3 分钟出结果

免费评估简历匹配度

数据来源:Himalayas

岗位信息来源于公开渠道,版权归原作者所有