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LabCorp

Global life sciences R&D services

Data Management Study Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Life Science.
  • At least two years of Data Management and/or Clinical Trials experience.
  • Conversance with databases and database terminology.
  • Strong technical aptitude.
  • Ability to use standard Microsoft suite of software products.
  • Well-polished, inclusive, and engaging written and verbal communication skills.
  • 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.

Responsibilities

  • Work with Clinical Data Management personnel to assist with assigned day-to-day activities.
  • Support the Clinical Data Manager during study start-up by creating protocol folders for study documentation and adding entries into individual protocol spreadsheets.
  • Act as a data liaison between Clinical Data Management and other Labcorp Drug Development departments and business units.
  • Consult with Medical Affairs via a Medical/Technical Affairs Request Form.
  • Collaborate proactively and reactively with Project Management regarding study questions.
  • Manage and resolve issues with Specimen Management.
  • Initiate data changes with the appropriate department and revise non-compliant requests.
  • Partner with other Labcorp Drug Development departments and business units, and provide integrated support and process improvements as needed.
  • Complete assigned Quality Assurance tasks while adhering to internal processes and regulatory standards, including quality-checking test files, delivering test files to clients and logging them into the metrics tool, obtaining client approval, and storing auditable documentation.
  • Provide ongoing client support during study maintenance, including addressing errors and client issues such as queries; participating in study-related meetings; collaborating with clients regarding study modifications; maintaining auditable documents; facilitating Data Management functions of end-to-end data lock processes; reviewing the data transfer calendar for accuracy; reviewing data file properties and error reports, informing Data Managers of findings and following up as needed; and ensuring assigned transfers are completed each day.
  • Attend corporate, departmental, and sponsor-related training to increase capabilities as a Data Management Study Coordinator.
  • Ensure uninterrupted client service by sharing technical knowledge and customer service skills with peers and backing up peers as needed.
  • Perform other duties as assigned.

Desired Qualifications

  • Customer Service experience.

About the Company

LabCorp

Global life sciences R&D services

Labcorp provides global life sciences and healthcare R&D services, supporting pharma, biotech, and crop protection clients with testing, safety assessments, and regulatory submissions. It conducts studies ranging from basic physicochemical tests to complex inhalation toxicology and uses specialized facilities to evaluate inhaled substances and ensure regulatory compliance. Its global presence and integrated suite of services enable clients to move projects from early development to product approval within one organization. Labcorp aims to help clients bring safe, effective products to market efficiently, advancing human health and scientific research.

Company size
10,001+
Company stage
IPO
Headquarters
Burlington, VT
Founded
1976

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