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Job Details

Senior Pharmacovigilance Associate

Company: Clinical Professionals Ltd
Location: Hampshire
Reference: J31885
Closing Date: 05 Mar 18
Type: Full Time
Salary (£): Negotiable
Benefits: Competitive Salary and extensive benefits package

Job Summary:

A global pharmaceuticals company with a flourishing UK pipeline in various therapeutic areas is currently seeking a Drug Safety professional who take work well within a team of other safety professionals on scientific and commercial elements.

Requirements:

Senior Pharmacovigilance Associate
Permanent
Full Time
Location: Hampshire/Wiltshire/ Berkshire
Competitive Salary and extensive benefits package.

A global pharmaceuticals company with a flourishing UK pipeline in various therapeutic areas is currently seeking a Drug Safety professional who take work well within a team of other safety professionals on scientific and commercial elements.

Company / Role Overview:
The company has large pipeline and has recently undergone a period of growth of both established product and a large clinical pipeline. This role will require at least 4 years of well-rounded Pharmacovigilance including in PSUR and signal management and willing to fuse this with some commercial/strategic input to future company project.
This closely knitted company/team will allow you to shape and develop PV processes and methods in drug/compounds and devices. While gain some exposure to some of the senior elements of the drug safety activities, with the possibility to act as Deputy QPPV and work on various projects in an international setting.

Benefits to you:
* Competitive Salary and Benefits
* Fantastic company that is growing year-on-year and currently have a large investigational pipeline and established products.
* Excellent working environment including onsite gym and canteen
* Will open the door and exposure to the senior leadership teams in the UK.

Main duties will include:
* Take the lead for the development of the PV System Master File, asking the main point of contact for other functional groups.
* Provide input into the PV communication function, specifically to the QPPV.
* Maintaining EU and RoW PV/Regulatory intelligence and legislative updates.
* Identify appropriate sources of information to retrieve relevant data for signal evaluation, data entry using ARISg.
* Provide scientific input and review for regulatory documents (PSUR's, DSUR's and PBRER's) in accordance with timelines.
* Investigating and presenting findings on several commercial projects.
* Developing knowledge of company's Device safety knowledge base.

My focus is on Pharmacovigilance covers both opportunities that are open to both Physicians and Scientists. Clinical Professionals (OnlyMedics) are the leading pharmaceutical staffing consultancy in Europe. We are the agency of choice for pharmaceutical professionals as we are the most knowledgeable recruiters within our specialist sectors and receive the highest number of jobs across the UK of all agencies- therefore you can leave your job search and career guidance safely in our hands

Pharmacovigilance, PV, Scientist, Associate, Senior Associate, Clinical Trials, QPPV, Dep QPPV, Medical Devices, Master Safety File, Case processing, safety communication, Pharmaceuticals, Biotechnology, Clinical Research Organisation, CRO, Wiltshire, Berkshire, Hampshire, Bath, Bristol, Medical Devices,

Apply for this job: Senior Pharmacovigilance Associate

Contact Information:

Address:  Clinical Professionals UK
3rd Floor
33 Blagrave Street
Reading
Berkshire
RG1 1PW
England
Tel:  0044 118 959 4990
Fax:  0044 118 956 0607
Website:  Visit Our Web Site

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