Resourcing Solutions
for Medical Affairs, Regulatory Affairs and Clinical Development

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.

Unique opportunity for a CRA to join this Global organisation as the only non medical member of the EU Clinical Team. You’ll manage and develop the whole spectrum of clinical and scientific activity for a Cystic Fibrosis product in Phase IV. CRO Management, KOL development remit and European travel are all part of this rare opportunity.

Are you looking to step out of Clinical Project Management into a role with less travel, where you can be pivotal in using your knowledge and background in promoting all aspects of Clinical Quality. You will joining a well established Quality team and partner with a global Clinical group based in the UK.

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.

Our client is a growing global pharmaceutical company with an excellent pipeline of products. Due to an expanding pipeline in the Neurosciences area they wish to appoint an experienced Clinical Research Scientist at to support their development in the Neurosciences Diseases area. This is a key role and will sit at Associate Director level within the organisation.

To join this respected Global Clinical Research Organisation as an Office Based Senior Clinical Research Associate (SCRA). You’ll manage site responsibility for clinical studies and line manage junior CRAs. In some cases you will act as the Lead CRA on projects and liaise with European Colleagues.

Our client is a leading biopharmaceutical company This is an excellent opportunity for an experienced clinical development physician to support the development of one or more new chemical entities in the Internal Medicine/ Immunology area from First in Man studies to pivotal Phase III studies through to regulatory submission.

A fabulous opportunity for an experienced CRA to move into a Senior position, co-monitoring CRAs in EMEA for International trials. Based from our Client’s impressive offices in Buckinghamshire.

A fantastic opportunity for a Pharmacy Manager to work within an established biopharma as part of the management team, overseeing pharmacy activity and IP dosing on an International scale.

Our client is looking to recruit an experienced Lead CRA / Study Manager with experience in coordinating global clinical trials to join a small expert team based in the UK. You must really enjoy co-monitoring as the role is heavily involved with partnering with the CRO teams. An outstanding ‘career’ opportunity and the chance to take ownership of some high profile and exciting study areas.