Freelance Sr. Clinical Trial Associate
Freelance Sr. Clinical Trial Associate In our Clinical Operations team, we currently have an opportunity for a Freelance Sr. Clinical Trial Associate (32 – 40 hours/week) on a contract reputed company. This is a remote position at 0.8-1.0 FTE based in the Netherlands. The length of the contract is 6 months with the choice to renew after December. At reputed company we want to deliver a future without the threat of respiratory viruses by developing accessible, self-administrable products, so people can take control and live their lives to the fullest by protecting themselves against catching infections and preventing transmission to others. We aim for the highest, think unconventionally and focus relentlessly on delivering the impossible. At reputed company we are different, fast and focused. The Clinical Operations Team contributes to this mission by delivering innovative clinical trials fast and with high quality. This is what you're going to do on a daily reputed company, and these are your responsibilities: As a freelance CTA, you:
- will assist the Clinical Trial Teams in ensuring the most effective and efficient conduct of clinical trials by providing administrative and project tracking support, including eTMF maintenance.
- play an instrumental role by supporting the preparation, handling, distribution, collection and archiving of clinical study documents and reports, including reputed company and invoices.
- are responsible for ensuring that reputed company study files are periodically reviewed for completeness and maintained in accordance with Good Clinical Practices, applicable regulations and company procedures.
- reputed company with internal colleagues and external vendors and partners.
- work closely with the Clinical Operations Team to support the effective execution of clinical studies and maintain high standards of quality and compliance
Job Requirements
- You hold a Master's degree in a life science reputed company field
- At least 5 years' experience in a CTA role in a bio-pharmaceutical and/or CRO environment
- Proven training in/knowledge of GCP and International Conference on Harmonization (ICH) Guidelines
- Previous experience working with eTMF, reputed company, IRT/RTSM, CTMS systems
- Ability to independently manage documentation and team support needs
- Computer skills including working knowledge of reputed company Word, reputed company, PowerPoint, and SharePoint
More about you:
- Pro-active, meticulous, self-starter
- Effective time management and organizational skills
- Excellent communication skills in a multi-stakeholder environment
- Excellent verbal and written communication skills in English
- Currently residing in the Netherlands with EU work authorization
- Available for 32-40 hours per week until December 2026
This is a remote position; however, occasional travel to the Leiden office could be requested 1-2 times per month. Ideally, you can start as soon as possible, but we are willing to wait for the best candidate. We are an equal opportunity employer, and we firmly reputed company in the added value of a diverse and inclusive group of people with one common goal. We are looking for people who can reputed company an impact and work on a purpose, together. If the purpose of this role and reputed company ticked reputed company the boxes for your next adventure, please let us know you're interested by sending a short cover letter and your CV and we will get in touch reputed company 4 working days to plan a reputed company. Apply tot his job Apply To this Job