PV Medical Writer - HOME BASED

Key People


Job ID :

13708


Company Type :

Staffing Firms


Industry :

Pharmaceuticals


Education Level :

Bsc


Address 1 :

United Kingdom,London,London,


Key Skills :

pv, pharmacovigilance, RMP, PSUR, Medical writer, medical writing, author, PBRERs, PBRER, signal det


Salary :

Up to £0.00 per annum


Date Posted :

29 Nov, 2018



Company Name :

Key People


Location1 :

London




Job Category :

Drug Safety Jobs


Experience :

Fresher


Job Type:

Contract


Travel Amount:

negotiable





Description

An excellent opportunity has become available for an experienced PV Writer to join my client on a home based contract basis.

Within this role you will be responsible for authoring Pharmacovigilance aggregate reports, including PBRERs, DSURs and RMPs. Evaluation of aggregate safety data and experience of signal management would be ideal. Project management experience would be a benefit.

Responsibilities:

*Evaluation of aggregate safety data, authoring of PV reports and signal management activities.
*Process implementation and ensuring process compliance.
*Create error-free reports and other outputs according to the defined specifications to ensure timely reporting of assigned job to project management.
*Undertake the QC activity for tasks performed by other team members on an ongoing basis.
*Identify and provide standards for gathering information for use in trend analysis and reports information to company management.
*Interact with the client on a regular basis to understand the client's requirement for a particular project and ensure expectations are exceeding the targets in terms of quality, quantity within the scope of time constraints.
*Creating or updating the SOPs, WINs as per project specific requirements.
*Responsible for training and mentoring of team members depending upon the project requirement.

Skills & Experience:

*Bachelor's degree in scientific domain.
*Significant Pharmacovigilance industry experience within a pharmaceutical company or at a CRO.
*Experience of authoring of Pharmacovigilance aggregate reports, including PBRERs, DSURs and RMPs, evaluation of aggregate safety data and experience of signal management.
*Good understanding of clinical development processes including principles of clinical study operations, and ICH-GCP guidelines.
*Experience of managing writing teams in Pharmacovigilance domain is desirable.
*Project management experience is desirable.

For further details about this role, or other opportunities within Drug Safety or Pharmacovigiliance, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@keypeople.co.uk


Company Name:

Key People


Headquarters:

Catherine House,Adelaide Street


Sector:

Staffing Firms


Country:

United Kingdom


Zipcode:

AL3 5BA


Website:

www.keypeople.co.uk


Employees:

less than 100


Industry:

Pharmaceutical


City:

St Albans


Phone No. :

01727 817 626


Key People is a recognised leading supplier of staffing and recruitment services to the Pharmaceutical, Scientific & Biotech industry. The company has been operating for over 20 years and has an integrated team of qualified recruitment consultants averaging more than 7 years of recruitment experience. Each consultant is a specialist recruiter for their market area, so they can provide full market advice to candidates and clients alike.

For more information,visit www.keypeople.co.uk.

View all Key People Jobs



© 2018 Jobsinpharma - 4ward Technologies Ltd All rights reserved.