Resourcing Solutions
for Medical Affairs, Regulatory Affairs and Clinical Development

We are recruiting for a Pharmaceutical client for a field based Medical Liaison Specialist. You will be focused on the cardiovascular area, working in a non-promotional role supporting late stage clinical studies, non-interventional studies and general medical affairs support.

We are recruiting for a Pharmaceutical client for a field based Medical Liaison Specialist. You will be focused on the cardiovascular area, working in a non-promotional role supporting late stage clinical studies, non-interventional studies and general medical affairs support.

A UK CRA opportunity for an experienced Monitor based in / or between Leeds or Newcastle, you will be field-based and take responsibility for a set of sites in this region. An opportunity to join a top tier Pharmaceutical company, working across therapeutic areas.

Our client are recruiting for a Principle Safety Scientist, who will work supported by a team of other Safety specialists and a wider Regulatory Affairs group. This is a busy and outgoing team and would suit an individual looking to return to Leeds or start a new life in the North. Although this is a 1 year fixed term contract, there may be future opportunities to transition into a permanent role although there is no guarantee of this.

This role is for a full or part-time CTA to join a small yet highly professional Japanese Pharmaceutical Company within their European Clinical Research Headquarters, located in Central London. You’ll assist with all clinical project administration and be a real asset to the whole team. This organisation knows the importance of a good CTA, and therefore will provide you with all the support you’ll require and include you fully in the team.

A role for a Medical Information Specialist where you will support a busy team in ensuring compliance of promotional materials, monitoring drug surveillance activities, liaising with 3rd party providers and the review of monthly reports.

We are looking for a Senior Consultant in the area of Health Outcomes to assist in pre-launch clinical and commercialization activities for a top tier Pharmaceutical organisation. You will looking for an interesting contract role, be capable of working independently and comfortable driving R&D and commercial colleagues in Brand Planning and Health Outcomes Research.

Fantastic opportunity for an experienced Regulatory Affairs Executive to concentrate their experience within this Global Leading Pharmaceutical Company. The role is based with impressive Surrey Offices and sits within the UK and Ireland Regulatory Team.

Fantastic opportunity on a 9 to 12 month maternity cover contract for a senior clinical professional to manage projects ensuring all activities are successfully implemented and completed in accordance with the scientific and regulatory requirements, project plan, within the agreed timeframe and budget and to high quality following all applicable international standards.

A true Project Management role where you will work in a Product Development function of a highly ambitious Biopharmaceutical organsiation, working on all aspects of product development plans, providing overall guidance throughout stages of development.