Medical Device CRAs available for assignment

All CRAs are experienced in conducting studies to ISO 14155 and familiar with the Medical Device Directive.

Experience of conducting studies in:

• Orthopaedic and Spine
• In-vitro Diagnostics
• Urology
• Wound Care

 Skills include:

Production of all documentation including:

• Clinical Investgatior brochure
• Clinical Investigation Plan (CIP)
• Case Report Forms
• Patient Consent Forms
• Investigator/Hospital Agreements
• Study Master files

Obtaining approval from research ethics committee

Obtainin competent authority approval

Selecting appropriate sites

Study Initiation visits

Monitoring visits

Study close downs

Report writing

 

If you are interested in recruiting one of our CRAs please contact Medvance Resourcing on 01757 270 044

 

 

« Go Back