Clinical Data Associate
美考伯医药信息咨询服务(上海)有限公司
- 公司规模:50-150人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2016-10-17
- 工作地点:上海
- 招聘人数:3人
- 工作经验:1年经验
- 学历要求:本科
- 语言要求:英语 熟练
- 职位月薪:5000-10000/月
- 职位类别:临床数据分析员
职位描述
职位描述:
Primary Responsibilities
Ensures clinical trial databases meet project requirements by:
Reviewing documentation and requirements for new projects and anticipating impact to Data Management (DM) standards/processes
Collaborating with appropriate project teams as needed to stay abreast of and changes that could affect data collection, cleaning and/or transfers
Ensures the plan for data management is properly executed by:
Understanding the requirements for study implementation and data collection
Maintaining organized, complete, and up-to-date study documentation
Creating or reviewing Transmittal Forms for a study, ensuring consistency with existing standards
Keeping supervisor informed of project status
Ensures the accuracy and consistency of clinical databases by:
Reviewing data and identifying errors/inconsistencies
Developing study data specifications, including data transfer specifications, system configuration specifications, and data validations.
Collaborating with appropriate project team to resolve data issues
Tracking outstanding issues and following-up until resolution
Preparing and validating ad hoc data listings as necessary
Ensuring that system bugs and needs for enhancements are reported to the applicable Product Manager and that any stop-gap programming is approved
Secondary Responsibilities
Maintains Quality Service and Departmental Standards by
Adhering to department processes and standards
Reading, understanding and adhering to applicable Standard Operating Procedures (SOPs)
Assisting in establishing and enforcing departmental standards
Participating in the review and updating of company SOPs related to department
Contributes to team effort by
Working with internal staff to resolve issues
Exploring new opportunities to add value to the organization
Helping others to achieve results
Performing other duties as assigned
Maintains Technical and Industry Knowledge by
Attending and participating in applicable company-sponsored training
Required Skills
Qualifications:
Education:
? Bachelor’s degree in Computer Science, Life Sciences or related field preferred, or equivalent experience required
Additional skill set:
? Ability to work independently in a group setting; ability to adjust to changing priorities
? Excellent attention to detail
? Strong interpersonal and communication skills, both verbal and written
? Strong documentation and organizational skills
? Ability to project and maintain a professional and positive attitude
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Primary Responsibilities
Ensures clinical trial databases meet project requirements by:
Reviewing documentation and requirements for new projects and anticipating impact to Data Management (DM) standards/processes
Collaborating with appropriate project teams as needed to stay abreast of and changes that could affect data collection, cleaning and/or transfers
Ensures the plan for data management is properly executed by:
Understanding the requirements for study implementation and data collection
Maintaining organized, complete, and up-to-date study documentation
Creating or reviewing Transmittal Forms for a study, ensuring consistency with existing standards
Keeping supervisor informed of project status
Ensures the accuracy and consistency of clinical databases by:
Reviewing data and identifying errors/inconsistencies
Developing study data specifications, including data transfer specifications, system configuration specifications, and data validations.
Collaborating with appropriate project team to resolve data issues
Tracking outstanding issues and following-up until resolution
Preparing and validating ad hoc data listings as necessary
Ensuring that system bugs and needs for enhancements are reported to the applicable Product Manager and that any stop-gap programming is approved
Secondary Responsibilities
Maintains Quality Service and Departmental Standards by
Adhering to department processes and standards
Reading, understanding and adhering to applicable Standard Operating Procedures (SOPs)
Assisting in establishing and enforcing departmental standards
Participating in the review and updating of company SOPs related to department
Contributes to team effort by
Working with internal staff to resolve issues
Exploring new opportunities to add value to the organization
Helping others to achieve results
Performing other duties as assigned
Maintains Technical and Industry Knowledge by
Attending and participating in applicable company-sponsored training
Required Skills
Qualifications:
Education:
? Bachelor’s degree in Computer Science, Life Sciences or related field preferred, or equivalent experience required
Additional skill set:
? Ability to work independently in a group setting; ability to adjust to changing priorities
? Excellent attention to detail
? Strong interpersonal and communication skills, both verbal and written
? Strong documentation and organizational skills
? Ability to project and maintain a professional and positive attitude
职能类别: 临床数据分析员
关键字: 临床数据分析员
公司介绍
BioClinica, Inc provides our clinical trial sponsors best-in-class centralized cardiac safety & efficacy services and independent medical image assessment solutions; all designed to facilitate successful new drug development in the pharmaceutical, biotechnology and medical device market sectors.
Built on over 27+ years of cumulative clinical research experience, BioClinica offers the world-wide biopharmaceutical industry unparalleled service quality, dedicated global capabilities and advanced technologies boasting a 100% on-time delivery of all projects. With a sustainable track record of medical and regulatory expertise, market leadership and proven operational processes, sponsors turn to BioClinica for trial design consultation and customized service offerings tailored specific to their unique needs.
BioClinica's extensive international experience is comprised of working alongside a broad spectrum of organizations across 600+ studies - Phase I - IV in over 60 countries around the globe. Our market leading medical imaging services are proven across more oncology trials than any other core laboratory. Our imaging and cardiac safety solutions are performed in a stringent quality controlled environment, ensuring GCP and 21 CFR Part 11 compliance.
We believe our employees are one of our greatest assets and we strive to attract and retain the highest caliber, professionally skilled and dedicated staff. If you are interested in making a difference in the quality of people's lives and working in an exciting environment that offers excellent compensation and benefits, then BioClinica is interested in you.
Built on over 27+ years of cumulative clinical research experience, BioClinica offers the world-wide biopharmaceutical industry unparalleled service quality, dedicated global capabilities and advanced technologies boasting a 100% on-time delivery of all projects. With a sustainable track record of medical and regulatory expertise, market leadership and proven operational processes, sponsors turn to BioClinica for trial design consultation and customized service offerings tailored specific to their unique needs.
BioClinica's extensive international experience is comprised of working alongside a broad spectrum of organizations across 600+ studies - Phase I - IV in over 60 countries around the globe. Our market leading medical imaging services are proven across more oncology trials than any other core laboratory. Our imaging and cardiac safety solutions are performed in a stringent quality controlled environment, ensuring GCP and 21 CFR Part 11 compliance.
We believe our employees are one of our greatest assets and we strive to attract and retain the highest caliber, professionally skilled and dedicated staff. If you are interested in making a difference in the quality of people's lives and working in an exciting environment that offers excellent compensation and benefits, then BioClinica is interested in you.
联系方式
- 公司地址:地址:span淮海中路