[上海]美考伯医药信息咨询服务（上海）有限公司

美考伯医药信息咨询服务（上海）有限公司
发布时间：2019-11-15 15:21:01
招聘职位：Imaging Research Associate（影像研究专员）
职位信息：
    职位类别：卫生专业技术人员
    学历要求：本科及以上
    招聘人数：5人
    工资：6000
    联系邮箱：Leanne.li@
    
    联系电话：021-64749310
    联系手机：15250958311
    工作地点：淮海中路1325号23楼
职位描述：
职位描述：

Primary Responsibilities

The Imaging Research Associate I, coordinates all site and operational activities, from study start to study close, to ensure the timely delivery of high quality service deliverables for assigned studies.

• Assist in preparation and reproduction of study materials during study start-up phase of clinical trials

• Follow up with outstanding documentations from clinical sites to complete site qualification

• Schedule logistical and technical trainings with site personnel

• Create test run requests for sites submitting digital data

• Review, process, track and monitor all study related data received from sites

• Assist in the monitoring and resolution of data discrepancies resulting from discrepancy listings generated from clinical data management

• Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors

• Investigate and complete logistical edit checks

• Report issues found with study systems (i.e. study data, reading analysis system)

• Perform day to day IQC activities including coordinating, requesting, tracking and processing of IQC data including:

  • Baseline, on-going, and end/interim analysis IQC Data Review

  • Coordination of cross calibration phantom rotation

  • Phantom data analysis and data entry

• Ensuring accuracy of tracking information in IQC Tracking and study tracking datas as pertaining to IQC and/or DXA scanner information

• Coordinating machine change instances for appropriate documentation and equivalence data collection

• Machine Equivalence analysis and processing

• Ensure IQC data is collected and maintained according to applicable SOPs and/or study protocol requirements

• Manage Baseline, Interim and End of Study IQC data submissions, track and report progress to study teams and ensure timelines are met

• Communicate with Bioclinica clinical study team and/or sponsor regarding deliverables

• Understand functions of software used to produce and collect IQC data

• BMD Scan Review Form preparation

• Study data maintenance (e.g., change of contact information)

Assists Project Managers with project administration by

• Planning and coordinating the site start-up activities

• Reading and understanding project protocol documents

• Entering, maintaining, and tracking of data in internal software

• Participating in project meetings, conference calls, and training calls

Assists Project Managers in maintaining, reviewing and communicating project progress by

• Reviewing and analyzing project tracking weekly

• Generates, tracks and resolves data queries

• Identifying site and data trends, and recommending actions to Project Manager

• Communicating and following up on project tracking discrepancies

• Assisting in monitoring data flow

• Generating, reviewing and distributing weekly/monthly project tracking reports

• Ensures the development and adherence to project timelines as they relate to therapeutic processes by

• Following up on outstanding items including missing data, incomplete paperwork, etc.

• Managing site communication, including distribution of subject data reports

• Assisting in tracking and resolving of client issues

• Scheduling and tracking completion of site training

• Serving as additional point of contact to client, sites, sponsors, etc.

• Keeping supervisor advised of current issues

Maintains client (internal and external) satisfaction by

• Responding to inquiries in a professional, courteous and timely manner

Maintains Quality Service and Departmental Standards by

• Reading, understanding and adhering toganizational Standard Operating Procedures (SOPs)

• Assisting in establishing and enforcing departmental standards

• Participating in the modification of company SOPs related to the therapeutic team

Maintains Technical and Industry Knowledge by

• Attending and participating in applicable company-sponsored training

Bachelors, Chinese, English, Qualifications:
Education:
High School Graduate Associate/Bachelor&39;s Degree
Experience:
Familiarity with PC-d computers and standard software packages including e-mail, word processors, Excel spreadsheets and datas.
Knowledge of the drug development/clinical trials process/basic clinical research and/or experience working in a pharmaceutical environment preferred
Knowledge of “good clinical practices” preferred
Familiarity with network navigation and file saving conventions, including moving/copying files and folders
Additional skill set:
Ability to work in group setting and independently; ability to adjust to changing priorities
Excellent attention to detail andientation toward meticulous work
Strong interpersonal and communication skills, both verbal and written
Ability to provide and maintain a professional and positive attitude
Leadership skills. ?Self-motivated with ability to work in teams with minimal supervision, with aggressive deadlines
Strong documentation andganizational skills
Goaliented

单位详情：
BioClinica在临床试验领域拥有30多年的经验，在全球范围内为4000多例试验提供了支持服务。我们的成像核心实验室使用创新技术，可高效地完成医学影像的交付、质量控制和分析。我们将专注于临床医疗的医学及科学团队与全球关键意见领袖网络相结合，可为申办者提供业界领先的专业技术和工作流程，帮助他们高效优质地完成临床试验。