How have DOCS become the leading provider of global resourcing solutions to the clinical development industry? It's simple, our client-based staff are supported by offices in over 40 countries, an experienced team of clinical research professionals, an industry-leading resourcing engine and a robust quality management platform.
The Operations Management (OM) service delivers an industry-leading approach to contract placement services, which results in a superior experience for both our clients and consultants.
Through one to one coaching and performance management OMs engage with our clients and consultants to ensure seamless on-boarding and alignment of responsibilities and expectations.
At the conclusion of each assignment, the OM will coordinate the completion of activities and comprehensive off-boarding.
Our Recruitment Consultants prepare and tailor the candidate shortlist and summaries based on the needs identified during the intake process and a tiered screening process that includes:
DOCS can also administer specific questionnaires or tests you require such as personality/behavioral profiles and language testing as well as arrange for interviews with customer representatives.
Our tried and tested recruitment methodology uses a 20-Step Global Delivery Approach that is broken down into 4 critical pieces:
The new feature rich website provides enhanced functionality with user friendly navigation.
DOCS’ 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.
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.