Similar posts
Pharmacovigilance Coordinator
This vacancy has now expired. Please see similar roles below...
This is a brilliant opportunity for a Pharmacovigilance Coordinator to join a renowned biopharmaceutical company who have approximately 25000 employees placed in over 170 countries, this particular role will be based in Maidenhead. This diverse company who specialise in research and development focus on producing strong clinical performances, assessable patient benefits and economic value. This Pharmacovigilance Coordinator will provide administrative support to the pharmacovigilance department and will support the ICSR Pharmacovigilance Manager and Head of Pharmacovigilance to meet the company's statutory pharmacovigilance responsibilities on behalf of the Medical Director.
Job Responsibilities:
- To comply with the company's policies and procedures to meet statutory, quality and business requirements within the overall strategy and objectives of the company.
- Responsible for the health, safety and environmental performance of themselves and others through compliance within EHS programs, regulations and standards. Subject to the policy and procedures outlined in the EHS Handbook.
- Ensure accurate & timely management of ICSR information onto local system; My ICSR (GAIT)
- Acknowledgment of ICSR receipt within a timely manner to report source
- Filing & Archiving
- Arranging meetings including room logistics
- Arranging hotels and flight bookings
- Raising departmental Invoices/Purchase Orders
- Pharmacovigilance administrative support as required
- Assist in additional ICSR follow up requests & support PV department
- Attending & Taking PV Meeting minutes
- Assists with all admin related activities during Audits and Inspections
- Support the training of affiliate personnel on relevant Pharmacovigilance responsibilities
Skills and Requirements:
- Effective and clear communication, both written and spoken
- Excellent organisational skills
- Excellent team working skills
- Excellent attention to detail
- Adherence to strict timeframes & timely completion of activities
- Knowledge of Pharmacovigilance desirable
- GCSE English and Maths or equivalent
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Weronika Ficek on +44 203 0789 550 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Related jobs
Highly Competitive
Germany
Proclinical is seeking a dedicated Order Management Team Lead to join our client's team for a remote role in Germany.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a QC Associate to join the Bioanalytics Microbial Team at our client's facility.
Highly Competitive
London, England
Proclinical is seeking a Lead Biostatistician with a focus on oncology to permanently join our client's team.
Highly Competitive
London, England
Proclinical is seeking a Medical Coding Lead with a focus on oncology.
Highly Competitive
Neuchâtel, Switzerland
Help bring science to life and join a leading pharmaceutical company, where you'll play a key role in delivering life-changing medicines through a world-class supply chain!
Highly Competitive
Bristol, USA
Are you ready to take your next step in your manufacturing career? This position performing large-scale bioconjugation processes for cGMP manufacturing projects is your next step!
Highly Competitive
Utrecht, Netherlands
Be the vital link between breakthrough science and patient care. We are on the hunt for a dedicated Manager to orchestrate seamless global delivery of investigational medicines!
Highly Competitive
Nordrhein-Westfalen, Germany
Medical Science Liaison (Pädiatrische Onkologie/Rare Disease) Gebiet West
Highly Competitive
Visp, Schweiz
Proclinical is seeking a User Manager for Electronic Systems to join and oversee user management tasks at our client's facility.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a CQV Engineer to join our client's team on a contract basis.