On-site Preclinical Study Coordinator

Inotiv, Inc.

Boulder (CO)

Hybride

USD 36 000 - 43 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Health and dental coverage
Short- and long-term disability
Paid time off
Paid parental leave
401(k)

Résumé du poste

Inotiv, Inc. in Boulder, CO is seeking a Study Coordinator to support the preclinical study process on-site. You will communicate with study directors, technicians, and vendors, manage initiation materials, and ensure compliance with GLPs, USDA, AAALAC and OLAW.

The role emphasizes data integrity, SOP adherence, and collaborative work across departments. Responsibilities include preparing data sheets, protocol amendments, and back-up support for Study Directors, with attention to detail and

Qualifications

  • Bachelor's degree in life sciences or related field with minimum 3 years in a pharmaceutical setting.
  • Strong written and verbal communication skills.
  • Excellent data management and ability to edit protocols, spreadsheets and reports.

Responsabilités

  • Maintain and submit study initiation materials.
  • Communicate with vendors, clients and stakeholders.
  • Order supplies for studies and schedule activities.
  • Ensure data sheets and lab math accuracy.
  • Assist in in-life study conduct and training requirements.
  • Ensure SOP compliance and participate in SOP revisions.

Connaissances

Communication
Editing documents
Microsoft Office
Attention to detail
Team collaboration

Formation

Bachelor's degree in life sciences

Outils

Microsoft Word
Microsoft Excel
Microsoft Outlook

Description du poste

Inotiv, Inc. in Boulder, CO is seeking a Study Coordinator to support the preclinical study process on-site. You will communicate with study directors, technicians, and vendors, manage initiation materials, and ensure compliance with GLPs, USDA, AAALAC and OLAW.

The role emphasizes data integrity, SOP adherence, and collaborative work across departments. Responsibilities include preparing data sheets, protocol amendments, and back-up support for Study Directors, with attention to detail and

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