Clinical study manager, remote and partly in fabulous Italy.

Would you like the comfort of working from your home, and getting the benefit of travelling to fashionable Milan? Then this is the right opportunity for you.

My client is a small innovative drug development company, which is growing rapidly thanks to their pipeline with new treatments.

They are looking to cure a previously thought to be incurable disease, thanks to their medicine kids can have a brighter future.

Work tasks:

Supervision of CRO and vendors.

• Co-monitoring visits at the sites
• Oversight of monitoring activities, such as review of monitoring visit reports, protocol deviations
• Manage screening and recruitment activities to ensure timely enrolment.
• Perform ongoing data review.
• Liaise with drug safety and medical monitors for safety issues and SAEs
• Review and approval of regulatory and ethics committee submissions.

Requirements:

• Minimum 5 years experience as a CTM
• Preferably worked as a CRA as well.
• Experience with orphan drugs and/or Neurology
• You will be on-site about 20-25% of the time

If this sounds like the right opportunity apply now as interviews are already ongoing.

K.Danielsson@nonstopconsulting.com

+46 850 927 950 internal extension is 8118

if this does not sound like the opportunity for you, but you are a professional within the pharmaceutical, medical device or biotech industry, please feel free to get in touch, to see other opportunities we may have within this field.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry..