Qualifications:
• Bachelor’s degree or nursing qualification is required. Scientific/health care field
preferred, but not required.
• Internal applicants: Minimum 2 years of intensive field monitoring experience as CRA I
• External applicants: Minimum 3 years of intensive field monitoring experience in
phase I-III clinical trials within a pharmaceutical company, CRO or similar organization.
Experience in oncology therapeutic area is desirable
• Strong knowledge of clinical research process and medical terminology
• In-depth knowledge of ICH-GCP guidelines and local regulations
• Knowledge of regulatory requirements and guidelines governing clinical research.
• Superior organization skills
• Strong attention to detail in composing and proofing materials
• Excellent analytical and creative thinking skills
• Ability to establishing priorities, scheduling and meeting deadlines
• Must have excellent English written and verbal communication skills
• Ability to reason independently and recommend specific solutions in clinical settings
• Must be able to work in a fast-paced environment with demonstrated ability to juggle
multiple competing tasks and demands under tight deadlines
• Ability to work successfully within a cross-functional team
• Strong knowledge of MS Word, Excel, PowerPoint and Outlook
• Driving license