Reference Number: JO-2007-452713
Senior Pharmacological Specialist
Job Type: Contract
Senior Pharmacovigilance Specialist
Contract until end of the year with likely yearly extension
Cheshire based – some work from home flexibility
Offering up to 450.00 Per Day DOE
Clinical Professionals is collaborating with an internationally recognized pharmaceutical firm who are looking for an experienced PV Specialist to join their established team. Reporting into the Inspection Readiness Lead you will be responsible for the management of assigned projects including continuous improvements, process updates and quality and compliance.
Job Responsibilities include;
Identify opportunities to improve and simplify processes and guidance, provide practical solutions and drive implementation.
Utilise knowledge of pharmacovigilance and associated regulatory and drug development processes to maintain and support the global inspection readiness strategy.
Participate in and/or support activities for GVP, GCP and GMP audits/inspections both globally and with local affiliates.
Working across CMO, identify issues and risks and propose options to mitigate them.
Working across CMO, support RCA and CAPA development and monitor completion.
Candidate requirements include;
Individual must be eligible to live and work in the United Kingdom
Life Sciences degree of the equivalent
Knowledge and experience of Pharmacovigilance processes and regulatory requirements
Experience of supporting major (FDA/MHRA/EMA) regulatory inspections in GVP and / or GCP area
Experience of working in the CAPA management process
If this position is of interest to yourself, please call Sophie at Clinical Professionals on 07526 003 117 or alternatively forward your CV to firstname.lastname@example.org.