Jobs at Houston Methodist

Provide direct nursing care and coordinate daily activities for neurology/Alzheimer clinical trials, ensure GCP and regulatory compliance, enroll and consent patients, collect/process specimens, document in CTMS, liaise with investigators/sponsors, and support quality, safety, and study financial processes.

Coordinate day-to-day clinical research activities: recruit and screen participants, obtain informed consent, collect vitals and labs, perform phlebotomy, maintain source documentation, prepare IRB and regulatory materials, assist with budgets and study initiation, and support PI and study team to ensure protocol compliance and participant safety.

Lead and manage international healthcare partnerships and advisory projects, building PMO discipline, overseeing scopes/timelines/budgets, driving business development, and coordinating cross-functional stakeholders to deliver projects aligned with partner goals.

Coordinate day-to-day activities of clinical research protocols: screen and interview patients for eligibility, schedule study visits, collect and enter clinical data into source documents and EDC/CTMS, maintain regulatory records, report adverse events under supervision, manage study supplies, and follow IRB and ICH/GCP guidelines.

Manage and oversee cGMP manufacturing projects: develop project plans, track resources, budgets, milestones and deliverables; ensure adherence to SOPs and cGMP/GLP regulations; support equipment validation, audits, batch record review, regulatory inspections, and cross-functional transition of research to compliant processes.

Senior scientific leader who defines and oversees innovation, implementation science, digital health, and AI-enabled research. Provides strategic oversight of study design, analytics, grant development, regulatory compliance, resource stewardship, mentorship, and scientific communication to advance translational, non–wet-lab research across multidisciplinary teams.

Support cGMP/cGTP manufacture of nucleic acid and cell-based therapies, perform aseptic handling, cleanroom procedures, batch and quality record review, assist with equipment/facility verification and audits, and follow regulatory standards (FDA, ICH, FACT, CAP, AABB) to ensure product safety, identity, strength, quality, and purity.