Pharmaceutical / Clinical Data Manager

Hays Life Sciences
Weybridge, UK
19 Jun 2019
26 Jun 2019
Contract Type
Full Time
Real World / Clinical Trial data manager for growing pharmaceutical company in London. Project management

Your new company
A well-established company in the pharmaceutical industry, based in the London area, that are currently undergoing strong growth.
The company has a consultancy arm that works closely with clients to provide Real World Evidence (RWE) and Real World Data (RWD) projects & services to allow clients to generate value out of their late phase data.

Your new role
You will be working closely with a wide range of clients and internal stakeholders to provide support to a number of late phase / real world evidence trials being carried out for a variety of therapy areas. You will be involved in managing the data capture, management and processes, and liaising regularly with clients and their clinical operations teams, eg PIs, Project Managers, site monitors, etc.

Major responsibilities will include:
  • Setting up and managing data capture (EDC) tools or systems;
  • Clinical data management;
  • Developing / helping to develop protocols, plans (eg monitoring plans) and SOPs;
  • Working closely with clients as a point of contact / troubleshooter for any data issues;
  • Managing stakeholder relationships to foster client engagement and help generate new/repeat business;
  • Ensuring any Adverse Events/SAEs are escalated to relevant pharmacovigilance teams;
  • Writing / reviewing reports for clients.

This is initially a 12 month contract, that may extend / go fully permanent

What you'll need to succeed
As well as strong communication, organisational and time management skills, you should have:

  • A BSc / MSc (or equivalent experience) in life sciences, statistics, economics, health economics, business or a related subject;
  • A track record of working within the pharmaceutical / clinical trials industry;
  • An excellent understanding of Electronic Data Capture (EDC) and/or Data Management from clinical trials (or experience as a site or in-house monitor/CRA);
  • Experience of protocol / SOP development and implementation for trials;
  • Project management skills, or an aptitude for this;

Hands-on experience with tools used for clinical data management.

What you'll get in return
The chance to work on a range of interesting projects in a great company atmosphere, along with a good salary package.
The company is growing, so there will be a number of chances to further develop your skills and career.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on 0203 465 0057.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

Keywords: Real, world, evidence, data, science, RWE, RWD, clinical, trial, management, protocol, SOP, EDC, capture, site, patient, operations, market, access, project, manager, management, client, consulting, consultancy, pharmaceutical, industry, drug, development, therapy, disease, statistics, business, commercial, strategy, outcomes, research

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