SciPro has partnered with a leading pharmaceutical organization that is seeking an experienced scientist to lead ADME efforts within a multidisciplinary team. This role focuses on advancing drug discovery and development through experimental design, data interpretation, and collaboration across various functions, contributing to regulatory submissions and therapeutic innovations.

Key Responsibilities:

• Deliver integrated data packages for compound selection, study design, and regulatory submissions.
• Collaborate across Discovery and Development teams to optimize ADME properties and advance drug candidates.
• Design and support nonclinical and clinical studies, ensuring regulatory compliance.
• Lead R&D initiatives to enhance ADME/DMPK capabilities across drug modalities.
• Integrate in vitro, in vivo, and in silico ADME data to refine structure-activity relationships.
• Represent ADME in regulatory discussions and guide scientists on modern ADME principles.

Qualifications:

• Ph.D. in Pharmacokinetics, Pharmacology, Pharmaceutics, Biochemistry, or related field with 6+ years of experience.
• Strong expertise in drug metabolism, disposition, and pharmacokinetics (discovery and development).
• Experience with molecular modalities (e.g., biologics, peptides, oligonucleotides).
• Proficiency in modeling software (e.g., SimCYP, GastroPlus).
• Excellent communication, collaboration, and project management skills.

Additional Information: This opportunity offers a chance to drive innovation and impact patient care while collaborating with a passionate R&D team.