Description
A leading CRO is looking for a CRA / SCRA to join their Ireland team for a 6 month contract.The role will be home based with 65% of the time monitoring across Dublin, Limerick and Cork.
Primary Duties:
- The CRA mus review regulatory documents as required and prepare site visit reports.
- Responsible for multiple projects and must work both independently and in a team environment.
- The CRA may participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training.
- May participate in clinical training programs and maintain awareness of developments in the field of clinical research as needed.
Requirements
- Prefer BS/BA- 2 yrs monitoring experience or combination of on-site monitoring and clinical research coordinator experience.-
- Customer service orientation.-
- Sound knowledge of medical terminology and clinical monitoring process.-
- In depth therapeutic and protocol knowledge as provided in company training.-
- Ability to perform travel an average of 65%, depending on project needs.-
- Excellent verbal and written communications skills.- In depth therapeutic and protocol knowledge as provided in company training.-
- Excellent interpersonal and organizational skills and attention to detail.-
- Computer literacy, proficiency in MS Office
This is an excellent opportunity to work for a fast moving organisation, offering competitive daily rates.
If you are interested in this position and would like some more information please send an updated CV to and call Hailey on .
Please also pass this opportunity onto anybody you know who may be interested in this as we do offer £250 referral vouchers.
Have a lovely day and I look forward to hearing from you