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.
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.
As a SSU you will be responsible for the independent preparation, review and approval of country related submission packages in accordance with ICH, GCP and all applicable regulations, laws and other guidelines and ethical standards Also responsible for the independent preparation, review and approval of site level critical documents for Investigational Product (IP) release in accordance with regulatory/sponsor requirements – within specific timelines and quality standards. Developing and finalizing Master and Country Specific Information Sheets/Informed Consent Forms (SIS/ICFs)
Effectively provide administrative support to the Quality Assurance department.
• Monitor and track Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information • Ensure all ICON, Sponsor, and regulatory timeframes are met for the processing and reporting of safety information • Assist in ensuring the completion of all departmental project activities accurately in accordance with ICON standards, regulatory requirements, and contractual obligations to Sponsors
Provides assistance to the ITG project teams and works to ensure quality, efficiency and improved profitability.
Provides support to the Call Center and Project Leader to ensure a high level of Customer Service/Support and Quality Systems.