Ref #: 37518

Employment type: Permanent - Full-Time

Location: Hungary Budapest

Posted: 09-May-2022


Conducting site evaluations post-feasibility to determine site suitability
- Performing site initiations
- Building and maintaining solid relationships with investigators and site staff to improve study set-up cycle times
- Developing site logistics and milestone plans
- Developing site visit plans and conducts monitoring visits
- Supporting site with focused patient recruitment strategies
- Coordinating the collection of data and resolution of discrepancies at site
- Coordinating and tracking clinical study and drug supply activities at site
- Providing point of contact for study information exchange and manages site issues
- Ensuring local clinical study compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOP)
- Ensuring quality data generation and conducting Source Data Verification (SDV), as required
- Performing site close-out
- Ensuring appropriate safety reporting and management of adverse events and adverse drug reactions
- Sharing study conduct ‘best practice’ to increase site productivity
- Developing action plans to address study related gaps e.g. site failing to achieve recruitment targets
- Preparing sites for audits
- Escalating site-related issues
- Exchanging information on site performance and issues
Minimum 1 year independent CRA on site experience
Life Science Degree