中国僵尸片,亚洲欧美国产另类视频,亚洲精品无码人妻无码,亚洲有码转帖,亚洲欧美精品伊人久久,97精品依人久久久

該職位已失效,看看其他機(jī)會(huì)吧

GLP項(xiàng)目助理 Project Coordinator

8000-12000元·13薪
  • 上海閔行區(qū)
  • 1-3年
  • 本科
  • 全職
  • 招1人

職位描述

生物藥項(xiàng)目化學(xué)藥項(xiàng)目創(chuàng)新藥項(xiàng)目GLP醫(yī)藥制造
Position Overview:
The Lab Project Coordinator will play a critical role in managing laboratory operations, ensuring project efficiency, and maintaining compliance with industry standards for clinical trials and research initiatives in Shanghai. This position requires strong organizational skills, attention to detail, and the ability to work collaboratively across multidisciplinary teams.
Key Responsibilities:
1. Project Management:
? Coordinate laboratory workflows and timelines for clinical trials, ensuring alignment with global and regional objectives.
? Coordinate with cross-functional teams (e.g., clinical research, data management, regulatory) to ensure seamless execution.
? Collaborate with international teams and local stakeholders to address logistics, sample management, and testing results
? Monitor project progress, proactively address bottlenecks, and adjust plans as needed.
2. Laboratory Operations:
? Ensure adherence to Good Laboratory Practice (GLP) and other regulatory requirements.
? Support the implementation of new testing methods and procedures under the guidance of senior scientists project wised.
? Collaborate with technical staff to optimize laboratory procedures and improve productivity.
3. Data and Reporting:
? Compile, analyze, and present laboratory data in a clear and concise manner for internal review and regulatory submissions.
? Maintain accurate records and ensure data integrity throughout the project lifecycle.
4. Compliance and Risk Management:
? Stay updated on industry regulations and implement best practices to mitigate risks.
? Assist in preparing documentation for audits and inspections.
Qualifications:
? Bachelor’s degree in Life Sciences, Biochemistry, or related field; Master’s preferred.
? 2+ years of experience in laboratory operations, clinical research, or a related role.
? Strong understanding of GLP, FDA regulations, and data management principles.
? Excellent organizational, communication, and problem-solving skills.
? Ability to work independently and as part of a team in a fast-paced environment.
Benefits:
? Competitive salary and equity opportunities.
? Comprehensive health insurance, paid time off, and professional development programs.
? Access to world-class laboratory facilities and global project exposure
查看全部

工作地點(diǎn)

上海市閔行區(qū)新駿環(huán)路760號(hào)

職位發(fā)布者

鄔女士/HR

立即溝通
公司Logo南京立順康達(dá)醫(yī)藥科技有限公司
康達(dá) SMO是 Novotech Health Holdings集團(tuán)全資控股的臨床中心管理組織,在上海、北京、南京、廣州、深圳、杭州等地設(shè)有分公司及辦事處。業(yè)務(wù)覆蓋至全國(guó) 28個(gè)省、自治區(qū)和直轄市。自 2017年成立以來(lái),康達(dá) SMO的業(yè)務(wù)在飛速增長(zhǎng),是近年來(lái)國(guó)內(nèi)規(guī)模發(fā)展最快的 SMO之一。
公司主頁(yè)