Vivo PK​/PD Sourcing Lead

• Coordinate external in vivo PK, PD, and PK/PD studies at CROs.
• Partner with internal stakeholders and CROs on study design, dose selection, sampling strategy, endpoints, and bioanalytical requirements.
• Review CRO proposals, protocols, data packages, and reports.
• Align internal teams and CRO partners on scientific objectives, deliverables, timelines, and expectations.
• Identify scientific risks and knowledge gaps and recommend practical solutions.
• Manage multiple drug discovery programs and competing priorities.
• Track requests, workflows, operations, logistics, and KPIs.
• Ensure compliance with external PK workflows and applicable SOPs.
• Maintain clear documentation and elevate scientific, quality, or timeline risks.
• Work independently and influence cross-functional stakeholders without direct authority.

• In vivo PK
• In vivo PD
• PK/PD
• Preclinical drug discovery
• CRO management/coordination
• Study design
• Dose selection
• Sampling strategy
• Bioanalytical requirements
• Data interpretation
• Small molecule, peptide, and/or large molecule PK
• Cross-functional collaboration
• Scientific communication
• Project/workflow management
• Risk identification and problem solving
• Matrix environment
• Reagent provision and/or in vitro biology workflows – beneficial

• Bachelor's:
  Relevant scientific discipline + 10+ years industry experience
• Master's:
  Relevant scientific discipline + 5+ years industry experience
• PhD:
  Relevant scientific discipline + 1–3+ years industry experience

Demonstrated expertise in in vivo PK, PD, PK/PD, and preclinical drug discovery.

Experience working with CROs and/or academia-industry partnerships.

Ability to work independently with limited supervision.

Strong written and verbal communication skills.

Ability to manage ambiguity, changing priorities, and multiple assignments.

Ability to influence stakeholders without direct authority.