Sunnikan is recruiting:
– A Clinical Research Auditor Consultant
Would you like to work at an international level, be involved in a wide variety of missions and projects at the forefront of clinical research, develop your skills, work on a close-knit team in a human-sized company?
After an initial training period of 6 to 8 weeks in Paris, join our team of Clinical Quality Management Consultants in Paris, Bordeaux, Nantes, Lille or another major city near an international airport. Remote work is a possibility!
Your Mission?
To contribute to guaranteeing patient safety and respect for their rights, to assess the compliance of processes and systems with applicable regulations, as well as contributing to ensuring the reliability of clinical data.
You will mainly carry out this mission through audits, but also, depending on your skills, through consulting, training sessions and updating clinical quality management systems, in France or abroad (Sunnikan operates in 40 different countries).
Sunnikan will consolidate your training, provide you with personalised mentoring and access to our unique knowledge databases.
Our expectations:
- an academic background in Life Sciences,
- training and experience in clinical quality management systems,
- an extensive knowledge of clinical research processes (including project management, regulatory processes, monitoring of investigational sites, data management, statistics, computerised systems validation, personal data protection, etc.)
- an extensive knowledge of the applicable standards (France, Europe, ICH, GAMP5…),
- clinical research audit experience (investigational sites, contract research organisations, centralised laboratories, other service providers, etc.),
- a high level of business English (B2 CEFR (Common European Framework of Reference for Languages)), both written and oral,
- locations in Fontenay-sous-Bois, Bordeaux, Nantes, Lille
- the ability to travel regularly in France and abroad,
- and, above all, high standards, rigour, a great ability to summarise, interpersonal intelligence and the drive to learn continuously in order to progress and to excel.
To recap : the need and the determination to be a member of a team on an international scale.
Experienced in clinical research, you will be ready quickly to perform audits.
To apply, please send us your CV with your cover letter to : recrutement@sunnikan.com
– A Pharmacovigilance Auditor Consultant
Would you like to work at an international level, be involved in a wide variety of missions and projects at the forefront of clinical research, develop your skills, work on a close-knit team in a human-sized company?
After an initial training period of 6 to 8 weeks in Paris, join our team of Clinical Quality Management Consultants in Paris, Bordeaux, Nantes, Lille or another major city near an international airport. Remote work is a possibility!
Your Mission?
To contribute to guaranteeing patient safety and respect for their rights, to assess the compliance of processes and systems with applicable regulations, as well as contributing to ensuring the reliability of pharmacovigilance data.
You will mainly carry out this mission through audits, but also, depending on your skills, through consulting, training sessions and updating clinical quality management systems, in France or abroad (Sunnikan operates in 40 different countries).
Sunnikan will consolidate your training, provide you with personalised mentoring and access to our unique knowledge databases.
Our expectations:
- an academic background in Pharmacy or in Life Sciences,
- training and experience in pharmacovigilance quality management systems,
- an extensive knowledge of the applicable standards (France, Europe, ICH, GAMP5…),
- an extensive knowledge of pharmacovigilance processes,
- pharmacovigilance audit experience,
- a high level of business English (B2 CEFR (Common European Framework of Reference for Languages)), both written and oral,
- knowledge of personal data protection,
- knowledge of computerised system validation,
- locations in Fontenay-sous-Bois, Bordeaux, Nantes, Lille
- the ability to travel regularly in France and abroad,
- and, above all, high standards, rigour, a great ability to summarise, interpersonal intelligence and the drive to learn continuously in order to progress and to excel.
Knowledge of other vigilances (materiovigilance, cosmetovigilance, etc.) and clinical trial vigilance is a plus.
To recap : the need and the determination to be a member of a team on an international scale.
Experienced in pharmacovigilance, you will be ready quickly to perform audits.
To apply, please send us your CV with your cover letter to : recrutement@sunnikan.com