Resourcing Solutions
for Medical Affairs, Regulatory Affairs and Clinical Development

A contract, for a Senior CRA or a Lead CRA to move towards Global Study Management. Also ideal for those looking to move from the CRO environment into Pharma / Biotech. Excellent long term career progression in an International environment.

An interim role for 11 months with the possibility of extension, providing expertise and technical support to International Market Applications, post marketing variations (labeling and CMC). Lead and facilitate product registration and lifecycle management for markets. Work within a dynamic and innovative Biotech group.

Interim Pharmaceutical Physician required for an International role within this global pharmaceutical company. You will support two of their biggest marketed products. Up to 12 months.

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.

We are looking for an enthusiastic, self starter, with experience in Clinical Pharmacology studies, to join an early phase unit of a leading Pharma organisation. You will study manage the trials through the CRO’s and assist in the co-monitoring responsibilities. Close working group, offering really interesting study work.

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.

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.

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.

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.