Study Coordinator Preclinical Research Studies-DART

Study Coordinator Preclinical Research Studies-DART

Greenfield, IN

In this role you'll combine your knowledge in Scientific Research and Organizational Support together to coordinate the activities of routine and non-routine studies, in compliance with the appropriate company standards, GLP and regulatory guidelines in a timely, efficient manner. Provide 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.

**This position is not open to fully remote work, once fully trained (2-3 months) this can have a hybrid work arrangement offering 2 days a week remotely and 3 days in the Greenfield onsite location.

Essential Job Duties:

• Provides administrative backup support for Study Directors on day to day study-specific activities or tasks.
• Serves as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable.
• Maintains complete, organized, and current study files including study schedule, protocol, and applicable correspondence. Drafts protocols and amendments for Study Director Review and approval.
• Ensures all client comments on protocols and amendments are addressed in a timely manner.
• Verifies the project schedule accurately reflects the requirements of the protocol.
• Initiates and submits scheduling request in CMS
• Monitors study progress and assures that schedules are updated appropriately.
• Schedules and participates in preinitiation and other study-related meetings, as required, and takes and distributes preinitiation meeting minutes.
• Addresses and reviews 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.
• Co-hosts client visit
• Assists the Study Director in monitoring the financial status of ongoing studies, including completion of work scope changes as applicable Independently uses project tracking
• Undertakes other administrative or scientific duties as assigned.
• Assist SD by ensuring that Animal Order Forms are in place.
• Communicate timelines to Principal Investigators (PI) and support groups as applicable.
• Pay rate $22-$30 per hour

• Bachelor's Degree and/or equivalent combination of education in a related science field. Experience may be substituted for education.
• Highly prefer candidates with 1+ years of hands on (animal) preclinical research experince.
• Prior experience working in DART (Developmental and Reproductive Toxicology) animal research studies is preferred but not required.
• Preferred but not required is 1+ years of experience performing either preclinical or clinical research studies including reporting and submittal of data
• Preferred but not required 1+ years of experience providing organizational and scientific support to research to study team preferred but not required.

• Your work directly connects to improving the lives of people and animals around the world!
• Great benefits that go into effect the 1st of the month
• 24 days of PTO in first 12 months of employment
• Onsite fitness center, tuition reimbursement, 401k match of 5%, opportunity to purchase Labcorp stock at discounted rates via ESPP, all lab work done at at Labcorp office is FREE of charge.