Study Coordinator II BioA

We have an excellent opportunity for aStudy Coordinator Ion our BioAnalytical Team in Greenfield IN.

Labcorp Drug Developments work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients lives while growing your career.

In this role you will be coordinating 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.

Essential Job Duties:

• Writes Study Protocols Methods and Reports
  • With minimal support and guidance drafts protocols methods amendments and reports; utilizing sources such as Documentum Toxicology protocols and client supplied information
  • Reviews study activities for compliance against protocol/SOW Standard Operating Procedure (SOP) Policies and regulatory agency guidelines.
  • With support assists Scientist with report preparation including table and figure preparation; compiles analytical information from operations teams.
  • Under direction of Scientist supports with Quality Assurance Unit (QAU) audits of study documents drafts responses as applicable and follows up with appropriate personnel to ensure that all responses and/or necessary document/raw data clarifications are completed within specified timelines.
  • Reviews client comments in protocol method drafts and reports with Scientist works with them to determine appropriate responses; addresses comments under guidance of Scientist to ensure all necessary document/data clarifications are completed in a timely manner.
  • Supports report production processes through finalization
  • Assists with archiving of study related materials
• Drives/Maintains Study and Client Communications
  • Efficiently communicate and serve as a secondary to support the Scientist with client contact on assigned studies.
  • Proactively communicates and interacts with study team other departments and clients as applicable.
  • Attends and engages in pre-initiation and other internal study-related meetings and attends conference calls; takes and distributes meeting minutes / action items as appropriate.
  • Support PMs and Scientists with preparing for and attends routine client visits.
  • With support manages data transfer to clients as requested.
• Drives/Contributes to Process Improvement/Adherence
  • Participates in the development and maintenance of standard report/table formats as needed.
  • Participates in the development and maintenance of standard protocol method and Sample Analysis Plan (SAP) formats as needed.
  • Identifies opportunities to increase the efficiency of daily/routine procedures and reporting methods; provides input on and assists with implementation of new technologies system changes and enhancements.
• Study/Timeline Management
  • With support plans prioritizes and manages own workload and multiple responsibilities.
  • With support uses project tracking systems as appropriate.
  • Manages standard projects and study designs and drives to increase study load over time.
  • Maintains well-documented organized and up-to-date study files including real-time study schedule updates as applicable.
  • Demonstrates active engagement with study progress/timelines.
• Actively promotes a team environment; identifies and escalates any activities that do not promote a team environment.
• Other related duties as assigned

Minimum Required:

• Bachelor of Science (BS) degree in science or related field preferred; experience may be substituted for education
• Ability to learn/utilize word processing software database spreadsheet and specialized software
• Excellent communication and interpersonal skills
• Excellent attention to detail
• Ability to prioritize organize and manage time

Application Window - 1/21 thru 1/31/2026

Pay Range: $24 - $25 per hour

All job offers will bebased on a candidates skills and prior relevant experience applicabledegrees/certificationsas well as internal equity and market data.

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical Dental Vision Life STD/LTD 401(k) Paid Time Off (PTO) or Flexible Time Off (FTO) Tuition Reimbursement and Employee Stock Purchase PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible toparticipatein the 401(k) Plan only. For more detailed information pleaseclick here.

Labcorp is proud to be an Equal Opportunity Employer:

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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