Teams at Maplight Therapeutics

Lead and oversee statistical programming for clinical development and regulatory submissions. Manage development/validation of SAS programs to produce SDTM/ADaM datasets and TLFs, ensure CDISC and regulatory compliance, partner with biostatistics, data management, clinical and regulatory teams, manage CRO/vendor relationships, and implement tools/process improvements. Perform hands-on SAS programming and support programming deliverables for submissions and study reports.

Support regulatory lead with IND/CTA submissions and agency communications, maintain regulatory documentation and correspondence logs, collaborate with CROs and cross-functional teams, monitor regulatory guidance, and support project goals. Hybrid role with occasional travel for in-person meetings.

Manage and operate the company contract management system; draft, review, negotiate, and administer clinical, supply, commercial, and other agreements; develop policies, templates, and workflows; train business users; manage outside counsel and vendors; and support legal, procurement, and finance systems integration while aligning contracting with company objectives.