Provide overall direction for the initiation, monitoring, completion and reporting of hematology/oncology studies. Provide supervision and oversight for a group of disease based teams. Ensure conduct of research studies in accordance with FDA guidelines, GCP and IRB and CTO SOPs.
REQUIRED: Master's Degree from an accredited institution, plus 2 years' experience in clinical research; OR Bachelor's Degree in science or health-related field, plus 4 years' experience in clinical research; OR Associate's Degree in allied health professions/any Bachelor's Degree, plus 5 years' experience in clinical research. Must have Clinical research certification (ACRP or SOCRA).
Excellent verbal, written and interpersonal communication skills. Possess sound knowledge of procedures and regulations specific to the conduct of hematology/oncology clinical trials; possess thorough knowledge of Good Clinical Practice Guidelines. Organizational ability sufficient to plan and direct the activities of the clinical research team. Demonstrate diplomacy, tact and a professional demeanor. Possess organization, analysis, motivation, supervision and prioritization abilities.Preferred Qualifications
Supervisory experience.Working Conditions / Physical Demands