Beschreibung
Freelance - Senior Expert Clinical Manager - Oncology - SwitzerlandOur client, a global top 3 pharmaceutical company with approximately employees currently seeks a Freelance Senior Expert Clinical Manager to come on board for 6 month.
You are responsible for operational aspects of one or more clinical trials (phase I-IV, Expanded Access, Investigator Initiated, registries and Compassionate use) under the leadership of the CTH.
Furthermore you have to support all scientific aspects of clinical trial(s) as assigned. Also you are responsible for program level activities as assigned with an entrepreneurial approach which requires the ability to multi-task on a wide spectrum of activities with an overall external focus.
Key responsibilities of the role will include, but not be limited to:
- Contributes to or manage simple clinical trial with minimal supervision by providing input and contribute to the development of protocols and related documents, in the ongoing scientific review of clinical data, and in trial data analysis, reporting and publishing.
-Prepare training materials and presentations related to the planning and conduct of the trial.
- Manage simple clinical trial under supervision from the senior clinical operations team. Write CTT meeting minutes. May deputise for the CTH at certain meetings. Ensure all assigned operational trial deliverables are met according to timeliness, budget, operational procedures and quality standards, SOPs and Business Guidance.
- Support the development, management and tracking of trial budget working closely with the appropriate partners. Accountable for accuracy and timeliness of trial information in all trial databases and tracking systems.
Requirements:
You should have more than 3 years technical and operational experience in planning, executing and publishing clinical studies within a pharmaceutical company or contract research organisation. Basic knowledge of oncology, hermatology, endorinology is a big advantage. Furthermore you should be able to work independently as well as working effectively in teams and support more than one clinical trial. Thorough knowledge of GCP (Good Clinical Practice), clinical trials design and fluent English are necessary.
This is you chance to come onboard into one of the leading global company and benefit from the great working environment/conditions and salary package.
For more information, contact Marcus Müller at Real Pharma on .
Keywords: clinical manager, senior, freelance, clinical trials, oncology, hematology, endocrinology, GCP, CTT, CRO, clinical data, analysis, SOP, reporting, 6 month, quality standarts, english, switzerland
To find out more about Real please visit www.realstaffing.com