Paramount Clinical Research: Clinical Research Associate II (CRA) – Berkshire
A great chance to join a leading, international Clinical Research Organisation is currently available for a Clinical Research Associate II (CRA). You can work either in the office, or there is potential to work field based if desired.
As a Clinical Research Associate II (CRA) your role is to identify, select, initiate and close-out appropriate investigational sites for clinical studies. You will monitor those sites in order to ensure that studies are carried out according to the study protocol, while making sure company SOPs and applicable regulations are adhered to.
Responsibilities of a Clinical Research Associate II (CRA) include;
-Having a good familiarity with ICH-GCP and appropriate regulations
-Familiarity with principles of investigator recruitment
-Co-ordinate all activities required to set up and monitor a study, including:
-Identify investigators
-Help in preparation of regulatory submissions
-Design patient information sheets and consent forms
-Coordinate documents translation, verification and back translations where required
-Ensure timely submission of protocol/consent documents/safety reports
-Pre-study and initiation visits
-Conduct regular monitoring visits
-Maintain all files and documentation pertaining to studies
-Motivate investigators in order to achieve recruitment targets
-Complete accurate study status reports
-Ensure the correct storage of drugs
-Keep the project manager regularly informed
-Process case record forms to the required quality standards
-Deal with Sponsor generated queries
-Ensure the satisfactory close-out of investigator sites
-Ensure correct archiving of files on completion of a study
-Co-operate with sponsor and QA personnel in the conduct of QA audits
-Participate in feasibility studies for new proposals
-Maintain patient and sponsor confidentiality
-To participate in mentoring of new staff up to Clinical Research Associate (CRA) level as appropriate
-Assist with marketing the company
This is a great chance to join an international leader and you will work on exciting global studies with excellent career progression.
To be considered you need;
-A medical/science background and relevant clinical experience
-Flexibility and willingness to travel at least 50% of the time
-Ability to review and evaluate clinical data
-Foreign language skills desirable
-Current full driving license essential
-Good oral and written communication skills
You will receive a generous salary, car allowance, healthcare, pension, gym, flexible working hours and lots more. This is an opportunity not to be missed!
For more information call Gareth on +44(0)121 616 5135 or apply now for instant feedback.
Keywords – Clinical Research Associate II (CRA), clinical, clinical research, clinical research associate, senior CRA, senior clinical research, clinical trials, clinical study, clinical studies, clinical associate, clinical monitor, clinical project, project manager, CRA, CPM
Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.
Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.
