Description
For my clients, a leading pharmaceutical company in the Basel area, I am currently looking for a CTA (Clinical Trial Associate). This is a project for 6 months with the possibility of being extended. You will be working in an international environment. This is a company that is known for their pioneering work.My client is looking for someone with the following experience:
Requirements:
- Cordinates trial deliverables.
- Ensures that a trial-level project plan is developed together with all relevant roles and progress of deliverables adequately tracked.
- Identifiying, assessing and communicates risks to all relevant stakeholders (e.g. CTT, CDPM, Order Alignment Meeting, etc) along with appropriate mitigation strategies to ensure supply continuity for all patients.
Tasks:
- Reviews clinical trial protocol and protocol amendments
- Writing clinical demand plans for a trial based on trial requirements
- Forecasting for clinical trial demands
- Corresponds with Clinical Supply Documentation Specialist to define an strategies according to study design, study timelines, involved countries and regulatory requirements.
- Creates and drives finalization of CPRs
- Coordinates the randomization of clinical supplies
If you are interested in this position, please do not hesitate to send me your up to date CV in Word format.
If you know anyone that could be interested in this position, please also feel free to send me there contact details.
I look forward to hearing from you.
Sebastian Spaniol
s.spaniol(@)realstaffing.com