Clinical Research Associate - Spain

I’m partnered with a global CRO who is looking for a Senior Clinical Project Manager based in Spain.

The Senior CPM will act as a matrix leader for the global clinical operations team under the supervision of the Clinical Operations Manager and will be accountable for the timely execution of specific tasks within the protocols.

Responsibilities

• Conduct feasibility, pre-study visits, site initiation visits, monitoring visits and/or close out visits as necessary
• Ensure that the monitoring team is trained on study specific procedures and aspects
• Coordinate and oversee project activities
• Manage the vendors involved in the study
• Ensure that the monitoring activities are conducted as well as regularly reviewing the activity of monitoring, remote monitoring, contact and telephone contact reports
• Update and check the Trial Master File (TMF) of the studies within Switzerland as well as ensuring that the site TMF are checked by the monitoring team according to CRO and Sponsor procedures

Requirements

• Degree in a scientific field
• In depth knowledge of GCP and techniques for the monitoring of clinical trials
• At least 5 years working as a Clinical Project Manager
• Fluent in Spanish
• Able to coordinate all the activities related to the management of local and international projects including managing interventional clinical trials, monitoring of clinical trials, and guaranteeing the security of information; preferably in CRO environment
• Work independently under the supervision of the Head of Clinical Operations Unit and Clinical Operations Manager
• Ability to interact with personnel properly and to manage the monitoring activities of CRAs (if required)

If you are interested in discussing this role in further detail, please don’t hesitate to apply or reach out to me: Roxanna.keshavarz@rbwconsulting.com / +44 1273 952187