Carbyne has partnered with a European publicly listed clinical-stage biotech company with exciting immuno-oncology pipeline to search & select a Pharmacovigilance Expert to support their global clinical development program.The role can work remotely 100% home-based anywhere in Europe with limited amount of travelling in the future. Ideally candidates should be based either in Germany or one of the following countries: Hungary Poland France Germany or UK.
The purpose of the role is to provide pharmacovigilance oversight for oversee pharmacovigilance the companys fully outsourced clinical trials.Responsibilities:- Oversee global clinical safety reporting activities and develop processes on the Sponsor side as appropriate.
- Ensure PV compliance with global regulations and industry best practices throughout all activities like safety date review risk management and signal detection with all stakeholders and collaboration partners.
- DSUR assembly and review.
- Oversight of PV service provider and CRO partners.
- Develop and maintain PV agreements with all vendors.
- Point of contact for PV related matters with all business partners.
Requirements:- Life Science / Medical degree
- Pharmaceutical industry experience including at least 3-4 years in clinical safety arena
- Deep understanding of clinical drug development process
- Computer literacy
- Fluent English required
- Critical thinking and pro-active attitude0
Should you be interested in the details of this vacancy please uploadyour CV and we will get in touch with you for confidential discussion.
Carbyne has partnered with a European publicly listed clinical-stage biotech company with exciting immuno-oncology pipeline to search & select a Pharmacovigilance Expert to support their global clinical development program.The role can work remotely 100% home-based anywhere in Europe with limited am...
Carbyne has partnered with a European publicly listed clinical-stage biotech company with exciting immuno-oncology pipeline to search & select a Pharmacovigilance Expert to support their global clinical development program.The role can work remotely 100% home-based anywhere in Europe with limited amount of travelling in the future. Ideally candidates should be based either in Germany or one of the following countries: Hungary Poland France Germany or UK.
The purpose of the role is to provide pharmacovigilance oversight for oversee pharmacovigilance the companys fully outsourced clinical trials.Responsibilities:- Oversee global clinical safety reporting activities and develop processes on the Sponsor side as appropriate.
- Ensure PV compliance with global regulations and industry best practices throughout all activities like safety date review risk management and signal detection with all stakeholders and collaboration partners.
- DSUR assembly and review.
- Oversight of PV service provider and CRO partners.
- Develop and maintain PV agreements with all vendors.
- Point of contact for PV related matters with all business partners.
Requirements:- Life Science / Medical degree
- Pharmaceutical industry experience including at least 3-4 years in clinical safety arena
- Deep understanding of clinical drug development process
- Computer literacy
- Fluent English required
- Critical thinking and pro-active attitude0
Should you be interested in the details of this vacancy please uploadyour CV and we will get in touch with you for confidential discussion.
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