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Strong employer brand plus metro location increases applicant density moderately.
Role requires regulated R&D supplier knowledge and CRO/lab experience, limiting cross-industry transferability.
Explicit 2-4 years plus domain-specific R&D supplier and documentation experience required.
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Support study planning, supplier management, and operational execution across multiple R&D programs.
Act as liaison between internal teams, CROs, laboratories, and suppliers to ensure timely study execution and documentation compliance.
Manage data, forecasting, risk metrics, shipping documentation, procurement, and regulatory document submissions to meet operational milestones.
Bachelor’s degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, Business Administration, Supply Chain, or related discipline.
2-4 years of experience in supplier management, project coordination, study operations, clinical research, or related field.
Experience with databases, planning tools, and document management systems.
Proficiency in Microsoft Office Suite, especially Excel and PowerPoint.
Experienced in coordinating cross-functional study operations and supplier management in fast-paced R&D environments.
Detail-oriented with strong organizational skills to manage multiple priorities and maintain documentation compliance.
Capable of managing vendor relations, operational planning, and risk tracking to support study lifecycle activities effectively.