Litholink / Laboratory Corporation Of America
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Data Management Study Coordinator
Labcorp is seeking a Data Management Study Coordinator to join our team in Shanghai, China.
The Data Management Study Coordinator is accountable for acting as the secondary liaison between Labcorp Drug Development and Sponsors, to ensure the successful management of global projects through compliance with the Labcorp Drug Development strategy, in order to deliver outstanding customer satisfaction.
1. Work in collaboration with Clinical Data Management personnel to assist in day-to-day activities as assigned.
2. Support Clinical Data Manager during start up.
Create protocol folder(s) for study documentation.
Add entries into individual protocol spreadsheet.
3. Act as a data liaison between Clinical Data Management and all other Labcorp Drug Development departments and business units.
Consult with Medical Affairs via a Med/Tech Affairs Request Form.
Collaborate with Project Management proactively and reactively regarding study questions.
Manage and resolve issues with Specimen Management.
Initiate data changes with the appropriate department and revise all non-compliant requests.
Partner with other Labcorp Drug Development departments and business units, and provide integrated support and process improvements as needed.
4. Complete Quality Assurance tasks as assigned, while adhering to both internal processes and regulatory standards.
Quality Check (QC) test files.
Deliver test files to clients and log into the metrics tool.
Obtain client approval and store auditable documentation.
5. Provide ongoing client support (study maintenance).
Address errors and client issues including queries.
Participate in study-related meetings.
Collaborate with clients regarding study modifications.
Maintain auditable documents.
Facilitate Data Management functions of end-to-end data lock processes.
Review the data transfer calendar and ensure that it is accurate.
Review the properties of data files and error reports. Inform Data Managers of any findings and follow-up as needed.
Ensure that all assigned transfers are completed each day.
6. Attend training to increase Data Management Study Coordinator’s capabilities (including corporate, departmental and sponsor-related training).
7. Ensure uninterrupted client service.
Support peers by sharing technical knowledge and customer service skills.
Back up peers as needed.
8.Other duties as assigned.
Bachelor Degree in Life Science.
2 years or more Data Management and/or Clinical Trials experience.
Conversant with databases and database terminology.
Strong technical aptitude.
Customer Service experience.
Well-polished, inclusive, and engaging communication skills (written and verbal).
Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional environment.
Ability to handle multiple tasks in a timely and professional manner under demanding conditions.
Ability to use standard Microsoft suite of software products.
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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