Lars Schroetke

Providing assistance to the Medical Monitor during study set-up, enrolment-, treatment- and close-out activities on global, multi-center Phase 1 to 4 open-label and double-blinded, randomized oncology and hematology protocols; supporting and mentoring members of medical and clinical team in protocol specific requirements and procedures

Assist and support the Principle and Senior Clinical Study Coordinators in the screening and monitoring of healthy volunteers and patients participating in clinical trials in the GSK CIC, working within the scope of current Regulatory, ICH GCP and GMP standards and requirements and according to relevant GSK Standard Operating Procedures.

Ensured the efficient running and ultimate success of clinical trials within the nursing department, maintaining a customer related focus, prepare and review study specific documents, attend and report progress meetings, control quality of study data and documents, maintain excellent communication channels