We are looking for a Clinical Research Associate to join a biotech company specialising in Neurology. As a Clinical Research Associate you will be responsible for ensuring that clinical trials are conducted in accordance with the protocol, standard operating procedures, good clinical practice guidelines and all applicable regulatory requirements.
The Clinical Research Associate will be responsible for the following:
Conducting site visits to ensure protocol and regulatory compliance
Conducting source document verification
Reviewing and verifying data collected during a clinical trial
Ensuring that all study documentation is complete and accurate
Ensuring that all adverse events are reported in a timely manner
Assisting with the preparation of study reports and presentations
The Clinical Research Associate should have the following skills:
Excellent communication and interpersonal skills
Ability to work independently and as part of a team
Strong attention to detail
Good organisational skills
Ability to work to tight deadlines
Excellent problem-solving skills
If you are interested, please apply with your CV attached.