Teams at Wave Life Sciences

Provide clinical leadership for assigned products across all development phases. Design, plan, and oversee clinical trials; ensure scientific integrity, regulatory compliance, and medical oversight. Collaborate with cross-functional teams and external vendors, interpret and disseminate study results, support translational medicine, represent the company to regulators and at scientific forums, and mentor/manage staff as needed.

Designs, executes, and interprets in vitro and in vivo ADME/PK/PKPD, TK, PPB and DDI studies for RNA therapeutics. Analyzes PK/TK data (NCA), manages internal and CRO DMPK activities, contributes to IND/CTA regulatory packages, and represents DMPK on cross-functional teams.

Serve as IT business analyst for GxP computerized systems supporting QA and Regulatory Affairs. Lead requirements elicitation, validation/qualification (CSV/CSA, IQ/OQ/PQ), change control, data integrity and backup strategies, vendor coordination, inspection readiness, and lifecycle maintenance for GLP/GMP laboratory and manufacturing systems. Partner with QA, manufacturing, facilities, and vendors to ensure compliant system administration and validation documentation.