Pharmacovigilance Specialist
Titel: Pharmacovigilance Specialist
Werkgever: Hays
Plaats: Provincie Noord-Holland
Provincie:
Locatie:
Provincie Noord-Holland /
Omschrijving:
Your new role
The Pharmacovigilance (PV) Specialist reports to the Pharmacovigilance Country Lead and is responsible for case management activities for Post marketing and Investigational products in the country/territory. He/She complies with PV processes and regulations, and the company policies and procedures for his/her country operation. This applies to all relevant safety information. The PV Specialist is qualified to function independently in the processing of Adverse Events. In your new role as a Pharmacovigilance Specialist you have to translate and process spontaneous and solicited / clinical trial adverse events reports from their country/territories and enter them into the Global Safety database or forward to a designated data entry center or contractual partners . Besides that you conduct follow-up and reconciliation of adverse events reports received from other the company operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners, as applicable. You make sure that the safety-related data is filed, stored and archived.
You comply with PV regulations and Global Safety policies/procedures, participate in individual case safety report compliance activities and identify and communicate potential safety issues . As a Pharmacovigilance Specialist you c complete and document required PV training within required timelines, p perform other activities as requested by the Pharmacovigilance Country Lead and a assist in preparation for audits/inspections for their country/territories and may participate in the audit and/or inspection.
What you'll need to succeed
In your role as a PV, you have to speak both Dutch and English fluently. Besides that you have a HBO/Bachelor’s Degree, with several years of experience within pharmacy or nursing or WO/Master’s degree in the paramedic/medical biology field. You have good knowledge of medical terminology and Microsoft Office.
What you'll get in return
A Pharmacovigilance Specialist position for at least a year in a great atmosphere.
Your new company
Multinational pharmaceutical company in North-Holland.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
Interesse?
Stuur ons dan je CV en motivatie toe door te klikken op onderstaande knop "Reageer op deze vacature".
Provincie Noord-Holland /
Omschrijving:
Your new role
The Pharmacovigilance (PV) Specialist reports to the Pharmacovigilance Country Lead and is responsible for case management activities for Post marketing and Investigational products in the country/territory. He/She complies with PV processes and regulations, and the company policies and procedures for his/her country operation. This applies to all relevant safety information. The PV Specialist is qualified to function independently in the processing of Adverse Events. In your new role as a Pharmacovigilance Specialist you have to translate and process spontaneous and solicited / clinical trial adverse events reports from their country/territories and enter them into the Global Safety database or forward to a designated data entry center or contractual partners . Besides that you conduct follow-up and reconciliation of adverse events reports received from other the company operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners, as applicable. You make sure that the safety-related data is filed, stored and archived.
You comply with PV regulations and Global Safety policies/procedures, participate in individual case safety report compliance activities and identify and communicate potential safety issues . As a Pharmacovigilance Specialist you c complete and document required PV training within required timelines, p perform other activities as requested by the Pharmacovigilance Country Lead and a assist in preparation for audits/inspections for their country/territories and may participate in the audit and/or inspection.
What you'll need to succeed
In your role as a PV, you have to speak both Dutch and English fluently. Besides that you have a HBO/Bachelor’s Degree, with several years of experience within pharmacy or nursing or WO/Master’s degree in the paramedic/medical biology field. You have good knowledge of medical terminology and Microsoft Office.
What you'll get in return
A Pharmacovigilance Specialist position for at least a year in a great atmosphere.
Your new company
Multinational pharmaceutical company in North-Holland.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
Interesse?
Stuur ons dan je CV en motivatie toe door te klikken op onderstaande knop "Reageer op deze vacature".
