Senior Clinical Research Associate Vienna A fantastic contract opportunity has arisen for an individual to join a highly prestigious global CRO located in Germany or Austria with the ability to remote work. This is an opportunity to perform and coordinate all aspects of the clinical monitoring and site management processes.
In this role you will: Clinical monitoring and site management process in accordance with company Standard Operating Procedures, ICH Good Clinical Practices, FDA guidelines and local regulations Conduct site visits to assess protocol and regulatory compliance and manages required documentation responsible for ensuring that data will pass international quality assurance audits Company representative in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel May assist clinical / project management on assigned projects
You will bring to this role: University degree in a science-related field, certified... health care professional or equivalent certification/licensure from an appropriately accredited institution Previous experience as a clinical research monitor Fluency in English Valid Driver's License where applicable Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures Effective oral and written communication skills Strong customer focus Strong attention to detail Effective organizational and time management skills Proven flexibility and adaptability Ability to work in a team or independently as required Good knowledge of Microsoft Office and the ability to learn appropriate software Effective presentation skills Ability to travel to clients when required
If you have the skills and experience for this opportunity and the ambition to take on this position, please call Khiana for further details or email your CV today.