研究经理- FSP
Study Manager- FSP
当我们的价值观一致时，我们能够实现的没有限制。
在Parexel，我们都有相同的目标——改善全球健康。从临床试验到监管、咨询和市场准入，我们提供的每项临床开发解决方案都基于一种特别的东西——对所做工作的深刻信念。
无论我们在Parexel做什么，都在为最终能惠及患者的疗法开发做出贡献。我们认真对待工作，以同理心去做，并致力于带来改变。
Parexel FSP正在寻找研究经理！肿瘤学优先
职位目的：
研究经理（SM）协助研究管理研究主管和研究团队进行临床研究的日常运作（例如，临床试验团队[CTT]会议记录、临床物资计划/跟踪、实验室样本跟踪、影像数据核对、状态更新报告、研究结束活动）。
主要职责：
可能包括但不限于以下内容。
临床试验操作执行
- 可能支持一项或多项研究
- • 可能负责范围有限的研究（例如，生存随访）
- • 可能负责跟踪研究时间表，并熟练使用项目管理工具
- 根据需要与跨职能团队沟通
- • 可能与内部和外部利益相关者（研究站点、供应商、委员会等）互动，以支持临床研究目标
遵守Parexel标准
- 遵守所需的培训课程
- • 准确完成工时表
- • 按要求提交费用报销单
- • 按要求更新简历
- 保持对Parexel流程、ICH-GCP和其他适用要求的了解并遵守
技能：
- 展示出良好的口头和书面沟通能力
- • 需要具备MS Office套件经验–包括Word、Excel和PowerPoint
- • 精通书面和口语英语
- • 精通当地语言（如适用）
- • 愿意根据公司重要会议要求出差
知识和经验：
- 药物研发经验有益但非必需
- • 治疗领域（TA）特定经验有益
教育：
- 本科/硕士/博士，具有2年以上临床研究经验
EEO声明
Parexel是一家平等机会雇主。符合条件的申请人将无差别地获得就业考虑，不因受法律保护的身份而有所区别，在美国包括种族、肤色、宗教、性别、性取向等。
查看英文原文
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.
Parexel FSP is looking for Study Manager! Oncology highly preferred
Job Purpose:
The Study Manager (SM) assists the Study Management Study Lead and study team with the operational
conduct of clinical studies (e.g., clinical trial team [CTT] minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities).
Key Accountabilities:
May include but not limited to the following.
Clinical Trial Operational Delivery
- May support a single study or multiple studies
- • May lead a study with limited scope (e.g., Survival Follow-up)
- • May be responsible for tracking study timelines and will be proficient in
project management tools
- Liaises with cross-functional lines as appropriate
- • May interact with internal and external stakeholders (study sites, vendors,
- 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
- • Proficient in written and spoken English
- • Proficient in local language (as applicable)
- • Willingness to travel as required for key company meetings
Knowledge and Experience:
- Pharmaceutical experience beneficial but not required
- • Therapeutic Area (TA)-specific experience beneficial
Education:
- Bachelors/Masters/PhD with 2+ years clinical research experience
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