Study Coordinator II Bioanalytics

Company: LabCorp
Location: Chantilly
Posted on: March 12, 2023

Job Description:

Get ready to redefine what's possible and discover your extraordinary potential at Labcorp Drug Development. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.
If you are looking for a company where you can gain exposure to a wide variety of science and explore a multitude of career paths across the drug development spectrum, consider working at Labcorp Drug Development as a Study Coordinator II on our BioAnalytical Team in Chantilly, VA. In this position you will coordinate the activities of routine and non-routine studies in compliance with appropriate company standards, GLP, GCP, GMP, and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they are involved in a timely, efficient, and quality manner. High volume of data and report delivery in addition.
Candidates given best consideration will have the following skills and experience:

• Proficient in Microsoft Excel and Microsoft Word
• Highly organized
• Works well independently
• Ability to multi-task effectively and navigate various systemsSchedule: This is a Hybrid work model with a combination of on site presence and remote based work. Core hours are 9:00am-3:00pm with flexibility on start and end times around core hours.
  Duties and Responsibilities:
  • Independently drafts protocols, sample analysis outlines (SAOs), amendments and study schedules as appropriate, using proposal outline or client-supplied information.
  • Reviews study compliance against protocol, SOP, and regulatory agency guidelines.
  • Learns to serves as the primary contact in communication and interaction with other departments and clients as applicable.
  • Updates and maintains project tracking systems as appropriate.
  • Participates in and assists Study Director/Principal Investigator (SD/PI) with pre-initiation and other study related meetings, including scheduling and leading meetings as required.
  • Learns to manage increasingly complex projects and study designs and/or increased study load.
  • Responsible for report preparation, including table and figure preparation.
  • Assists in 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 and submits audit responses for approval as appropriate.
  • 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 through finalization, including archival of data as appropriate.
  • Assists with routine client visits as requested. Manages data transfer to clients as requested.
  • Assists SD/PI in monitoring study phases.Education, Qualifications, and Experience:
    • Bachelor's degree or equivalent in life sciences or chemistry
    • Minimum of 2 years of related experience
    • Ability to utilize word processing software, database, spreadsheets, and specialized software
    • Excellent communication, presentation, and interpersonal skills
    • Excellent attention to detail
    • Ability to prioritize and manage timeA combination of education, training, and experience will be considered.
      Labcorp is proud to be an Equal Opportunity Employer:
      As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. We encourage all to apply.
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Keywords: LabCorp, Chantilly , Study Coordinator II Bioanalytics, Other , Chantilly, Virginia