Case studies that describe our placements for clinical research professionals:
Our client needed a specialist to create documentation in support of the EU-Directives for medical devices. The Clinical Evaluation verifies the clinical safety and performance of the device. Our contract professional has been assisting in manuscript preparation and working cross functionality with other teams and divisions for the past 4 years.
Auditor for clinical research
Our client, a mid-sized medical device company, needed a contractor to provide clinical research monitoring and assist with site auditing, primarily in Greater Minneapolis/St. Paul. They also needed someone to assist with standard operating procedure (SOP) development and clinical trial master file review. Talencio sourced an experienced professional to assist the client for this strategic three-month project.
Designing clinical trials
Our client, a Minneapolis-based medical device company, advances the treatment of chronically ill patients. They sought assistance in creating well-designed clinical studies and assisting with evaluation of trial management and providing recommendations for improvement. Talencio sourced an experienced contract clinical research professional for this key project.
Senior clinical trial specialist
Our client, a world-wide leader in its clinical category, was in need of a Clinical Research Professional for a long term project (1-2 years) . The responsibilities were significant and included: study site liaison, clinical data management, managing clinical study documents, dissemination of data, device allocation, investigator site training meetings, etc. Talencio found a perfect match with nearly 10 years of experience in Clinical Research roles.
Integrity | Dependability | Practicality | Collaboration | Tenacity | Trustworthiness | Experience