Job Description :
Our client is a global pharmaceutical developer and are currently looking to expand the Global Drug Development team with an addition Senior Study Management Associate.

The SnSMA report into the Principle SMA and generally there would be 2/3 SnSMA's working on a particular study, they would be responsible for certain Countries within the Study, and would work closely with the Country CRA's and sites.
This position could be best described as an in-house CRA, they would not monitor, however they would co-monitor and train CRA's in their designated Countries, so it is important that they have been a CRA, for a good few years.
The ideal candidate will need to have had exposure to full project life cycle of a study and must have UK experience.
They should have had some experience of mentoring more Junior CRA's and have had exposure to reviewing monitoring reports.
This role is above and beyond the traditional monitoring CRA role and is all about mentoring, planning, escalation of issues and management of issues, taking that accountability.

This role would give an experienced CRA the opportunity to move away from a heavy based monitoring role and allow them the opportunity to get the bigger picture, gaining responsibility for their own Countries, as well as International exposure.

This is an office based full time role, standard office hours are 9am - 5.15pm (there is no real flexibility around this).

CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23485 in all correspondence.

Keywords: Study Management, SCRA, Clinical, Clinical Recruitment, Drug Development