PV Medical Writer

Key People

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Job ID :


Company Type :

Staffing Firms

Industry :


Education Level :


Address 1 :

United Kingdom,Hertfordshire,Hertfordshire,

Key Skills :

PV, medical writing, medical writer, pharmacovigilance, drug safety

Salary :

£45 - £55 per hour

Date Posted :

06 Feb, 2019

Company Name :

Key People

Location1 :


Job Category :

Medical Writing Jobs

Experience :


Job Type:


Travel Amount:



An excellent opportunity has become available for an experienced PV Writer to join my client based in Hertfordshire - 2 days home working is possible.

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.


*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 or email tbarratt@keypeople.co.uk

Company Name:

Key People


Catherine House,Adelaide Street


Staffing Firms


United Kingdom






less than 100




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.

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