Whether you are a Pharma or CRO employee, a job seeker or a registered contractor our market knowledge, global recruitment network and operational infrastructure enable us to meet your recruitment and career needs.
Our dedicated FSP Delivery Platform™ allows us deploy functional resourcing solutions which combine our global resourcing engine with clinical development expertise. Clients benefit from reduced costs, improved quality, enhanced productivity and accelerated cycle times.
As part of ICON plc, DOCS' FSP Delivery Platform™ leverages ICON’s extensive therapeutic, geographic and functional expertise to ensure greater efficiencies across client programs.
You need a trusted partner for permanent placements. Our experienced specialist recruitment consultants will gain a close understanding of your requirements and company culture. They will then use our large global database and candidate pool to source the best fit for your business.
Our processes are designed to deliver a quality result and are effective across all functions, position types and volume.
DOCS provides clients with full-spectrum contract staffing solutions for clinical development. We fill all position types within the industry and can easily scale our global teams to match client requirements. Our experienced Operations Managers take responsibility for oversight of client-based personnel to ensure high quality results and seamless extension of the sponsor teams.
Pin-pointing top talent for leadership levels within your company requires a specialist and exclusive recruitment search.
Our Executive Search team is expert in the art of sourcing tactics and direct search methodology. They will find the best candidates for local and international Life Sciences senior-management positions. We also offer bespoke services, including niche projects, which may be unsupported elsewhere.
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MayThe new feature rich website provides enhanced functionality with user friendly navigation.
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FebDOCS’ parent company, ICON plc, today announced that it has agreed, subject to closing conditions, to acquire the Clinical Trial Services Division of Cross Country Healthcare, Inc. (NASDAQ:CCRN), a leader in healthcare staffing services. The transaction is expected to close during the first quarter of 2013.
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MayDOCS will be attending at the ICON exhibit at The 5th DIA China Annual Meeting
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MayTo arrange a meeting with the DOCS and Assent team at PharmaSUG 2013, contact us
La société: Notre client est un leader mondial au savoir-faire reconnu dans les dispositifs médicaux cardiovasculaires figurant parmi le TOP 5 des fabricants de pacemakers, défibrillateurs implantables et de valves cardiaques. Date de début du contrat : asap Poste : Ingénieur Traitement de signal / Biomédical – BAC+5 minimum Durée : Prestation de 3 mois renouvelable 1 fois Poste basé à Clamart – déplacement ponctuel à prévoir à Rennes
Do you have monitor experience and are you looking for a broad Clinical Research Associate role on a National level? Apply!
Heb je ervaring als Regulatory Affairs Officer en wil je ervaring opdoen binnen de R & D afdeling van een marktleider in generieke medicijnen die zich in sterke mate bezig houdt met de ontwikkeling, productie en verkoop van innovatieve geneesmiddelen? Solliciteer!
Do you have more then ten years of Global Project Management experience on multinational trails and are you looking for a new challenge at a fast-growing academic research organization? Apply!
Our client is a global, research-focused healthcare company with Group Headquarters in Basel, Switzerland. They have played a pioneering role in UK healthcare since 1908. Today, they are the leading in-vitro diagnostics company in the UK and the leading provider of pharmaceutical treatments for cancer and viral diseases. They are also a major supplier of medicines for the treatment of transplantation, virology, bone and rheumatology and renal anaemia. In total, their UK pharmaceutical and diagnostics businesses employ nearly 2,000 people. As part of their expansion, there are looking to recruit for a Clinical Trials Assistant to be responsible for the co-ordination and support of high quality Clinical Trials and projects, ensuring standardisation and consistency of delivery across studies in accordance with current best practices: meeting the requirements of the specific brand strategy and thereby supporting the UK Pharma business.