Hobson Prior are seeking a CTA to join a global CRO on a permanent basis located in with the ability to do hybrid working. Our client is focused on cardiovascular disease.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• Day to day operational support to Lead Ops, CPMs, CRAs for defined tasks during study.
• Collect, co-ordinate and maintain essential documents and the Trial Master File (TMF).
• Investigate logistics and monitor meetings organised comprising of the development of presentation materials under direction of PM.
• Provide cover for the study telephone.
• Active membership of projects meetings: meetings booked, minutes taken and communicated.
• Document learning and recommendation from study debriefs and best practice identified and implemented in collaboration with manager and colleagues.
• Develop and distribute of newsletters for investigators and monitors.
• Study area managed according to standards including set up, access rights and maintenance of study related documents.
• Development and maintenance of study specific documents and tracking tools under direction of PM
• General filing and adhoc administrative task.
• Provide correct documentation to support the preparation of clinical study reports and publications.
• Track Health Authority/ IRB submissions and approvals.
• All documentation completed correctly.
• Issues escalated as appropriate.
• Aware of and compliant to laws and regulations applicable to projects.
• Be aware of and compliant to all policies and procedures including: Finance, Procurement, IT and Legal.
• Attend all requisite training sessions and completion of all requisite on-line training and compliance programmes within specified time limit.

Key Skills:

• Good accuracy and attention to detail.
• Excellent written and verbal communication skills.
• Excellent IT knowledge and capabilities.
• Ability to work well in a team.
• Excellent planning and organising skills.
• Ability to speak additional languages would be a plus.

Requirements:

• Eligibility to work in the UK is required to be considered for the role.
• Experience in full project life cycle monitoring is required.
• Previous experience in a CRO and/or Pharma environment is desirable.
• Understanding of regulations and SOPs.
• Ability to manage smaller projects/tasks.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.