AstraZeneca is looking for a Clinical Research Associate (CRA) in Oncology to ensure the quality and efficiency of clinical studies at allocated centers, working collaboratively with study teams to meet commitments and deliver timely results.
Requirements
- Minimum 2 years of CRA experience in Oncology therapeutic experience required
- Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
- Good knowledge of relevant local regulations
- Good medical knowledge in relevant AZ Therapeutic Areas
- Basic understanding of the drug development process
- Good understanding of Clinical Study Management including monitoring, study drug handling and data management
- Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment
Responsibilities
- Preparation, initiation, monitoring and closure of an agreed number of centers in clinical studies according to AZ Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations.
- Deliver according to the commitment in the individual trials.
- Work in close collaboration with other Monitors and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner.
- Ensure the delivery of the studies at allocated centers.
- Actively participate in the local study team(s).
- Monitor clinical studies according to AZ Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations.
- Manage study drug handling and data management.
Other
- Bachelor’s degree required, preferably in Life Science field
- Fluent knowledge of spoken and written English
- Ability to travel as required, 50-70%
- Excellent written and verbal communication skills, negotiation, collaboration, and interpersonal skills
- Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines
