Clinical Project Lead

Description

• Lead and manage the planning, initiation, execution, and closure of clinical studies
• Develop study protocols, case report forms (CRFs), informed consent forms (ICFs), and study manuals
• Oversee site selection, feasibility assessments, and initiation activities
• Overseeing clinical operation to assure that
• Conducting registered and non-registered clinical studies of products
• Preparing and authoring protocols and patient record forms
• Clinical trials are run complying GCP, SOP, guidelines and regulatory requirements consistently
• Clinical trials are run to meet projects requirements and objectives according to agreed planning, prioritisation and budget
• Resource and schedule planning of a trial including the selection of appropriate vendors

Qualifications

• Min. 2 years in study management
• Min. 5 years of experience in clinical research
• Bachelor’s degree in a medical or science related field: MSc. or BSc. preferred
• Fundamental knowledge of therapeutic area and products, preferred.