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Clinical Trial Assistant
Location | United Kingdom |
Discipline: | Clinical Research |
Job type: | Permanent |
Contact name: | Roxanna Keshavarz |
Contact email: | roxanna.keshavarz@rbwconsulting.com |
Job ref: | 22381 |
Published: | over 2 years ago |
Expiry date: | 26 Jul 2023 11:59 |
Clinical Trials Assistant
United Kingdom
I am working with a medium sized CRO that is looking for a Clinical Trial Assistant (CTA) to support their clinical team across the UK working in an administrative position.
Responsibilities:
- Audit TMF to ensure all require regulatory documentation are collected and lead
- Administer clinical trials according to good clinical practices and standard operating procedures
- Facilitate process improvement initiatives to develop a clinical research database system to manage protocols
- Revise and review informed consents to ensure all GCP and ICH compliance
- Maintain the quality and completeness of study master files across programs in compliance with GCP
- Support the setup, data entry and QC of the system to ensure accuracy and quality of data
Requirements:
- Strong background in areas such as: nursing, pharmacy, health care management or life sciences research
- Highly proficient in software applications such as Word, Excel and PowerPoint
- Strong database skills
- Degree in life sciences or similar field
If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail:
?01273 952187
? roxanna.keshavarz@rbwconsulting.com
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