Back to search.SEC Recruitment Ltd - QA AUDITOR
| Employment Type: | Permanent |
| Location: | Russia |
| Salary: | £30000 - £40000 per annum + BENEFITS |
| Languages: | Russian |
Our client is looking to hire a QA Auditor for Eastern Europe.
The candidate´s main responsibility will be to conduct clinical audits in Eastern European countries to ensure compliance with SOPs, ISO 9000 requirements, study protocols and GCP guidelines.
The candidate will be involved at all stages of clinical trials, both in-house and at investigator sites, and will be working closely with both project teams and clients.
The candidate will also be responsible for the induction and training of personnel in areas that include GCP and ISO 9000.
The qualified candidate must possess a background in medicine, science and/or other relevant discipline. Previous experience in Clinical Quality Assurance Auditing is required. Must be familiar with GCP guidelines and relevant clinical trial regulations. Ability to review and evaluate clinical data/records is essential. Excellent communication and interpersonal skills.
This position is to be based in Russia or in some Baltic states (office based) with 40% international travelling involved
If interested, please send your CV to Nasiya Sharmarke or alternatively contact us in the number dispayed below
The candidate´s main responsibility will be to conduct clinical audits in Eastern European countries to ensure compliance with SOPs, ISO 9000 requirements, study protocols and GCP guidelines.
The candidate will be involved at all stages of clinical trials, both in-house and at investigator sites, and will be working closely with both project teams and clients.
The candidate will also be responsible for the induction and training of personnel in areas that include GCP and ISO 9000.
The qualified candidate must possess a background in medicine, science and/or other relevant discipline. Previous experience in Clinical Quality Assurance Auditing is required. Must be familiar with GCP guidelines and relevant clinical trial regulations. Ability to review and evaluate clinical data/records is essential. Excellent communication and interpersonal skills.
This position is to be based in Russia or in some Baltic states (office based) with 40% international travelling involved
If interested, please send your CV to Nasiya Sharmarke or alternatively contact us in the number dispayed below
You cannot apply for this job as it is no longer active.
