Description
Our client, an internatioal pharmaceutical company, is currently looking for a Senior Global Clinical Trial Associate (CTA), for a 6 month project in Basel. The Senior Global Clinical Trial Associate (CTA) role requires the following skills:Major Accountabilities
- several years of experience in the pharmaceutical industry.
- Ensure all operational trial deliverables are met according to timelines, budget, operational
- procedures, quality/compliance and performance standards under the management of the CTH. Assigned responsibilities can include development of specific sections of protocol and related documents; development of study tools; guidelines and training materials; management of clinical study material; oversight of vendors and other third parties; implementation of issue resolution plan; conduct clinical data review.
- Prepare clinical outsourcing specifications. Responsible for management of Contract Research Organizations CROs) and ensure adherence to scope of work within timelines and budget.
- Support the development, management and tracking of trial budget as assigned, working closely with the appropriate partners in Oncology Global Development (OGD and GMA).
- Manage interactions with relevant line functions including Data Management, Drug Supply Management country organizations under the direction of the CTH. Attend Clinical Trial Team (CTT) meetings, participate and report study progress and issues/resolution plan at the Clinical Trial Team meeting.
- Responsible for accuracy of trial information in all trial databases and tracking systems.
- Responsible for the ongoing scientific review and validation of clinical data (member of the Data Review Team).
- Participate in the organization and logistics of various trial-related committees.
If you are interested please feel free to contact me to the discuss the role in more detail.
Sebastian Spaniol
s.spaniol'@'realstaffing.com