Labcorp
BioanalyticalStudyCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Bioanalytical Study Coordinator at Labcorp. Skills: Study Coordinator, Bioanalytical, Report Preparation. Draft sample analysis outlines. Review study compliance against protocol”
Industry & Context.
Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all necessary report/raw data clarifications are completed
What They're Looking For.
Must Have
Bachelor Degree in pharmacy, pharmaceutical analysis or chemistry, 3 months or more experience using computer and office software applications (e. g. Microsoft Word, Excel, MS-Access and Outlook)
Nice to Have
Two years of study coordinator for small molecule, Experience on a variety of studies performed in the department and exposure to a diverse client base, Knowledge of regulatory agency guidelines, Efficient use of word processing software, database, spreadsheet, and specialized software, Proficient in concise writing. Writing should require little or no external review or edit, Adherence to grammar, punctuation, composition, and spelling according to company standard conventions
What You'll Do.
Draft sample analysis outlines
Review study compliance against protocol
Communicate and interact with study team
Assist in development and maintenance of standard report/table formats
prioritize and manage own workload
Independently use project tracking systems
Improve processes to increase efficiency
Participate in and assist Study Director/Principal Investigators with meetings
Responsible for report preparation
Compile analytical information from laboratory groups
Manage increasingly complex projects
Assist in interpreting and evaluating data
Maintain well documented
organized and up-to-date study files
Review QAU report audits
Submit audit responses for approval
Follow up with appropriate personnel for clarifications
Review client comments and make decisions
Responsible for report production processes
Assist SD/PI in monitoring study progress
Schedule study phases
Maintain awareness of financial status of ongoing studies
Perform other related duties as assigned
How You'll Work.
Team & Collaboration
Communicates and interacts with study team, other departments and clients as applicable; Participates in and assists Study Director/Principal Investigators with pre-initiation and other study related meetings as required; Follows up with appropriate personnel to ensure that all necessary report/raw data clarifications are completed within specified timelines; Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all necessary report/raw data clarifications are completed; Assists SD/PI in monitoring study progress; Schedules study phases in coordination with SD/PI and lab operations
Communication Scope
Excellent communication; presentation; interpersonal skills
Process & Methodology
Plans, prioritizes and manages own workload and multiple responsibilities, Ability to manage increasingly complex projects and study designs and/or increased study load, Maintains an awareness of the financial status of ongoing studies, including work scope changes
Full Job Description
**Bioanalytical Study Coordinator** Labcorp is seeking a **Bioanalytical Study Coordinator** to join our team in **Shanghai, China**. **Job Responsibilities:** • Independently drafts protocols; sample analysis outlines (SAOs), amendments and study schedules with some oversight, using proposal outline or client-supplied information. • Reviews study compliance against protocol, SOP and regulatory agency guidelines. • Communicates and interacts with study team, other departments and clients as applicable. • Assists in the development and maintenance of standard report/table formats as needed. • Plans, prioritizes and manages own workload and multiple responsibilities. • Independently use project tracking systems as appropriate. • Learns to improve processes to increase the efficiency of daily/routine procedures and reporting methods. • Participates in and assists Study Director/Principal Investigators with pre-initiation and other study related meetings as required. • Responsible for report preparation, including table and figure preparation. Compiles analytical information from laboratory groups. • Ability to manage increasingly complex projects and study designs and/or increased study load. • Assists in interpreting and evaluating data for reports. • Maintains well documented, organized and up-to-date study files including study schedule, protocol and correspondence as applicable. • Reviews QAU report audits. Submits audit responses for approval as appropriate. Follows up with appropriate personnel to ensure that all necessary report/raw data clarifications are completed within specified timelines. • Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all necessary report/raw data clarifications are completed. • Responsible for report production processes through finalization, including archival of data as appropriate. • Assists SD/PI in monitoring study progress. • Schedules study phases in coordination wit
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