For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
Responsible for reviewing all study data to ensure it is complete and GLP compliant. Ensure that all data received for review follows SOP and regulatory guidelines that apply to the recording of study data. Interact with Scientist, QA staff and other departments with regards to data.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Complete data review on all paper and electronic data produced in operational departments.
• Ensure all forms that require data review and electronic data are in compliance with Standard Operating Procedures (SOPs) and forms are updated as needed.
• Ensure all data corrections are completed by the appropriate staff members and that they are completed correctly.
• Communicate with department management and Scientist regarding any issues related to data collection that impact the recording of data.
• Assist in departmental training by providing assistance with training on correct methods of data notation and correction as it relates to study data review.
• Assist in revising and developing department forms.
• Archive, collate, and organize all completed and reviewed data and/or file as appropriate.
• Interact with the Scientist regarding data that is received for review. Collaborate with QA staff to ensure GLPs are being followed for the recording of data.
• Assist with department filing as needed.
• Perform all other related duties as assigned.
The pay for this position is between $21.00 and $23.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
Job Qualifications
QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) required. Associates Degree preferred.
• Experience: None.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None
• Other: Strong organizational, communication and listening skills with acute attention to detail. Basic understanding of processes used for study data collection. Basic understanding of SOPs, FDA GLPs and GCP and other applicable regulatory guidelines governing the recording and review of study data. Basic understanding of algebraic math and scientific concepts. Ability to work effectively as a member of a team. Experienced computer skills; familiarity with Microsoft Office software and specifically with Word and Excel. Ability to work effectively under minimum direction.
PHYSICAL DEMANDS:
• Regularly operates a computer and occasionally operates other office productivity machinery such as a label maker, copy machine, and computer printer.
• Regularly communicates with employees.
• Regularly provides information to and receives information from/through various technologies, media, sources and contacts. Must be able to exchange accurate information in these situations.
• Specific vision abilities required by this job include close vision and the ability to adjust focus.
• Regularly moves about inside the office to access file cabinets, office machinery, etc.
WORK ENVIRONMENT:
• General office and laboratory working conditions, the noise level in the work environment is usually quiet.
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
帮助您找到属于您的时刻
当您向我们申请工作时，您会非常小心和努力。请放心，我们将同样努力寻找适合您的职位。我们的招聘流程如下：
职位搜索
了解 CRL、我们的文化以及我们为何开展我们的工作，同时寻找与您的兴趣和专业知识相匹配的职位。
申请
创建个人资料并申请您感兴趣的多个角色。
注意：根据职位的不同，您可能需要在申请中包含简历。
评估和申请审查
如果需要，请完成评估，以确定该职位是否适合您，反之亦然。招聘人员将根据职位要求审查您的简历和资格，并确定后续步骤。
注意：在此过程中的任何时候，您都可以登录您的个人资料以查看您的申请状态。
面试
通过与多元化的面试官会面来参与我们的包容性面试流程，他们将提供有关公司、文化和您的角色的信息，同时还会向您提出问题以评估您的技能、兴趣和专业知识。这也是您提问的好时机。
注意：Charles River 根据我们的 DNA（关注、领导力、责任心和团队合作）利用基于技术和行为的方法来提问。请熟悉 DNA 并准备好将您的经历与它们联系起来。
工作机会和入职
通过电话或电子邮件从 Charles River 招聘人员或招聘经理处接收有竞争力的录用通知书。录用通知书将包括您的头衔、工资、地点和其他相关信息。
注意： 接受后，您将与招聘人员一起确认入职日期，并在入职之前收到需要以电子方式完成的文件。对于美国的职位，一旦您接受，您将需要进行就业前药物筛查并通过犯罪背景调查。
职位搜索
了解 CRL、我们的文化以及我们为何开展我们的工作，同时寻找与您的兴趣和专业知识相匹配的职位。
申请
创建个人资料并申请您感兴趣的多个角色。 注意: 根据职位的不同，您可能需要在申请中包含简历。
评估和申请审查
如果需要，请完成评估，以确定该职位是否适合您，反之亦然。招聘人员将根据职位要求审查您的简历和资格，并确定后续步骤。
注意：在此过程中的任何时候，您都可以登录您的个人资料以查看您的申请状态。
面试
通过与多元化的面试官会面来参与我们的包容性面试流程，他们将提供有关公司、文化和您的角色的信息，同时还会向您提出问题以评估您的技能、兴趣和专业知识。这也是您提问的好时机。 注意: Charles River 根据我们的 DNA（关怀、领导、拥有和协作）利用基于技术和行为的面试问题。请熟悉 DNA 并准备好将您的经历与它们联系起来。
工作机会和入职
通过电话或电子邮件从 Charles River 招聘人员或招聘经理处接收有竞争力的录用通知书。录用通知书将包括您的头衔、工资、地点和其他相关信息。 注意： 接受后，您将与招聘人员一起确认入职日期，并在入职之前收到需要以电子方式完成的文件。对于美国的职位，一旦您接受，您将需要进行就业前药物筛查并通过犯罪背景调查。
特色职位
Charles River每时每刻都在发生重要的事情。这意味着您可以探索令人兴奋的新职业机会。今天就申请吧！
寻找其他岗位？搜索所有职位。
每时每刻
在 Charles River，您将能够为令人难以置信的突破做出贡献，同时体验令人兴奋的成长和发展机会。
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运营助理
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项目协调员
管理关键设施相关项目
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采购主管
管理采购、运输、库存和收货
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副经理
推动持续改进项目和设施建设
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萨拉·霍塔奈宁，工商管理硕士
芬兰库奥皮奥
萨拉·霍塔奈宁，工商管理硕士
芬兰库奥皮奥
支持您的福祉
您的奉献和热情为世界各地的人们带来了拯救生命的改变。我们致力于为您提供福利，提高您的生活质量。
财力
- 收益+激励
- 退休福利
- 假期+外出度假
- 认可
- 员工援助基金
职业
- 专业发展机会
- 职业发展
- 奖项
- 教育支持
健康和保健保险
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社会与社区
- 包容文化
- 11 个员工资源小组 (ERG)，成员人数超过 3,000 人
- 带薪志愿者休假的机会
- 社区外展+配套礼物+参与活动