Non-clinical Compliance Specialist - London, United Kingdom - Hobson Prior
Description
Hobson Prior are currently looking for a Non-Clinical Compliance Specialist to join a brilliant biotech organisation on a permanent basis located in London.
Our client is focused on creating solutions that may have the possibility of curing those who suffer from serious illnesses.
Please note that to be considered for this role you must have the right to work in this location.Key Responsibilities:
- For this role, you will manage the preclinical division documentation storage and retention aligned with site processes.
- Recognise and document possible procedural and documentation concerns.
- You will partake in the precision and updated maintenance of SOPs and training records across the team.
- Evaluate and approve nonclinical study documentation which involves authoring and/or evaluating study protocols and study reports of nonclinical studies in a timely manner.
- Any other assigned duties.
Key Skills:
- A high attention to detail.
- A selfmotivated individual.
- An organised individual who is able to manage own time efficiently and know how to prioritise workload.
- Capable of resolving issues.
- Communication skills both verbally and in writing.
- Works well both independently as well as in a team.
- Able to represent self in a professional manner.
Requirements:
- Educated to a degree level in a scientific field, though an advanced degree would be ideal but is not necessary for the role.
- At least 1 year of experience working within a QC or nonclinical study setting.
- Familiarity with quality documentation evaluation and approval, such as traceability, document IDs, completeness of study documentation.
- Acquaintance working in a quality and data documentation setting, preferably within a pharmaceutical organisation.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe.
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