In Vivo PK/PD Coordinator

📋 Description

• Coordinate external in vivo PK, PD, and PK/PD studies at CROs.
• Ensure compliance with external PK workflow and study requirements as outlined in SOPs.
• Understand and work with internal stakeholders and external CRO to participate in devising study
• Facilitate externally conducted studies by aligning internal teams and CRO partners on objectives
• Review proposals, protocols, data packages, reports, and execute studies in a timely manner.
• Identify risks and knowledge gaps, resolve barriers, and recommend practical paths forward.

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline with 10+ years of industry experience
• Demonstrated expertise in vivo PK, PD, PK/PD, and preclinical drug discovery.
• Small molecule, peptide, and/or large molecule PK experience is preferred.
• Experience with reagent provision and/or in vitro biology workflows is highly beneficial.
• Experience working with CROs/Academia-industry partnerships and cross-functional scientific teams.
• Ability to influence without direct authority and operate independently with limited day-to-day

🎁 Benefits

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Eligibility for yearly goal-based bonus & merit-based increases
• Compensation: $65,000-$80,000 per year based on education and related experience