Teams at Maplight Therapeutics

Support clinical operations across all trial phases: manage TMF and study documents, coordinate systems access, liaise with sites/CROs/vendors, prepare meeting materials and minutes, maintain trackers, assist with clinical trial insurance and data review, and ensure compliance with SOPs and ICH-GCP.

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.

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.