Description
A global CRO are looking for a CRA or SCRA to come on board ASAP for a 6 month contract.The ideal candidate will be based in the south or midlands and willing to travel to the north. The role will be home based with 65% travel to monitoring sites.
Primary Duties:
- Review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment.
- 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, organising 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:
- BS/BA- 2 yrs monitoring experience or combination of on-site monitoring and clinical research coordinator experience
- Customer service orientation.
- Studies are Haematological Oncology, so experience in this area is a must
- Sound knowledge of medical terminology and clinical monitoring process.
- In depth therapeutic and protocol knowledge as provided in company training.
- Ability to perform regionalised travel an average of 65%, depending on project needs.
- Excellent verbal and written communications skills.
- Excellent interpersonal and organisational skills and attention to detail.
- Computer literacy, proficiency in MS Office.
If you are an experienced CRA with Haematological Oncology experience and would like some more information please send an updated CV or call . Please also pass this opportunity onto anybody you know who may be interested in this as we do offer £200 referral vouchers.