Study Coordinator
Study Coordinator
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Job Description
Why People choose to work at Labcorp:
At Labcorp it is our people that make us great its what our clients our partners and most importantly what our employees say. Here you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.
We have an exciting opportunity for a Study Coordinator for Preclinical (Animal) Research Studies in Madison WI.
Position Summary:
The Study Coordinator is responsible for coordinating the activities of routine and non-routine studies in compliance with the appropriate company standards GLP and regulatory guidelines in a timely efficient manner. General assistance to Study Directors will be an essential part of the role and additional non-study specific support may be given to key clients. Additional daily duties may include support of other functions within Safety Assessment.
Essential Duties:
- Provides administrative and scientific support for toxicology studies including pre-study tasks (e.g. protocol development costing scheduling) monitoring the in-life progress of assigned studies and interacting with clients.
- Provides administrative backup support for Study Directors on day-to-day study-specific activities or tasks.
- Learns to ensure study compliance with the protocol standard operating procedures Good Laboratory Practices and other regulatory guidelines.
- Learns to plan prioritize and manage a workload and the associated responsibilities.
- Serves as a contact along with the Study Director in communication and interactions with other departments and clients with assistance as applicable.
- Learns to compile data for clients for regular study progress updates.
- Learns to draft protocols and amendments for Study Director Review and approval.
- Ensures all client comments on protocols and amendments are addressed in a timely manner.
- Schedules and participates in pre-initiation and other study-related meetings as required and takes and distributes pre-initiation meeting minutes.
- Learns to address and review quality assurance audits relating to protocols and amendments and reports (as applicable) with oversight. Follows up with appropriate personnel to ensure all necessary document/data clarifications are completed in the specified timelines.
- Prepare shipping documentation including CITES application requests and any other associated shipping documentation as required per study
Education/Experience:
- Bachelors degree in a related science field
- 2 years of previous related job experience
- Strong knowledge of office software (e.g. Microsoft Office especially Word and Excel)
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) Tuition Reimbursement and Employee Stock Purchase Plan. Casual PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan 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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Required Experience:
IC
Employment Type
Full-Time
