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Job Details

Pharmacovigilance Manager

Company: Kinapse Ltd
Location: Wimbledon (remote working considered)
Reference: 00028
Closing Date: 16 May 18
Type: Full Time
Salary (£): Competitive
Benefits: Competitive

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Job Summary:

Typical projects will involve processing of cases related to pharmacovigilance for any of Kinapse’s clients. The processing of information may include filtering, cleaning, migrating, analysis, reporting or publication of data and information. A project in Pharmacovigilance may also include PV report preparation, including, but not limited to, PSUR/PBRER, DSUR and RMPs, signal management and safety evaluation report preparation, or tailored PV client support.

Requirements:

An exciting opportunity has arisen for a Senior Pharmacovigilance Manager. Although our offices are in Wimbledon, we can accommodate home working.

Kinapse is recognised as a leading advisory and operational services provider to the global Life Sciences industry. The company provides its services across the full R&D and commercialization life-cycle, collaborating with its clients to improve the lives of patients, through a unique Advise – Build – Operate delivery model. Headquartered in the UK, Kinapse has over 700 staff located in Europe, Asia and USA.

As a member of our Operational Services team, you will interact with some of the world’s leading scientists and physicians on critical therapeutic and scientific issues. You will be passionate about communicating to a variety of audiences and be able to add a creative edge and maintain the highest quality standards. You will play a critically important role in executing outsourcing projects for our global pharma clients and will work as part of high performing teams on challenging assignments involving the processing of complex scientific, medical and technical information. 

Typical projects will involve processing of cases related to pharmacovigilance for any of Kinapse’s clients in strict adherence to the Standard Operating Procedures and Work Instructions valid at that time and may be subject to internal or external audit. The processing of information may include filtering, cleaning, migrating, analysis, reporting or publication of data and information. A project in Pharmacovigilance may also include PV report preparation, including, but not limited to, PSUR/PBRER, DSUR and RMPs, signal management and safety evaluation report preparation, or tailored PV client support.

You will be a key member of the project management team and oversees successful project governance from initiation, execution and completion of project(s) for Kinapse’ Global clients. You will also be responsible for the training and mentoring of team members.

You will have a strong academic background in a life science discipline and relevant Pharmacovigilance experience either in a pharmaceutical company or with a CRO. You will have an understanding of pre and post marketing pharmacovigilance processes including principles of clinical study operations, GVP and ICH-GCP guidelines. Experience in managing teams in Pharmacovigilance domain is preferred. You will also possess strong written and oral communication skills, commitment to highest quality outputs, high attention to detail, a professional service mentality, and an ability to build rapport and strong relationships with both internal and external colleagues.

Kinapse is a fast-growing, values driven company with a supportive team and can offer you a rewarding and challenging career working with smart, ambitious, yet humble professionals. We offer both office and home-based roles, and a competitive salary with a range of benefits including life insurance and health cover, pension and bonus.

If you want to be part of a progressive, forward-thinking company and want to make a difference we would really like to hear from you!

Apply for this job: Pharmacovigilance Manager

Contact Information:

Address:  Head Office
Tuition House
27-37 St George’s Road
London
SW19 4EU
England
Website:  Visit Our Web Site

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