This person will participate in the day-to-day management of CRO Data Management activities (i.e., development Data Management Plan (DMP), develop and annotate CRF's, develop database specifications, design or oversee the development of edit check specifications and programs, adherence to timelines and data expectations, etc.
Contracted Weekly Hours : 38.5 Rosemount Care Home is a 60 bed home offering general nursing care including, short term, intermediate, respite and palliative care. Our team of RGNs are extremely well trained to cater for all our residents needs.
Our client is a leading research-focused healthcare group, in the diagnostics space. With continual organizational growth and strong pipeline, their regulatory affairs team is looking to bring in a new regulatory affairs principal specialist or manager.
Leading Pharmaceutical fortune 200 company with over 25,000 employees globally is seeking to expand its team in the Bay Area. While the company is international, this team has more of a small company feel, looking for the right cultural fit for this Sr.
This position is responsibly for the overall direction, coordination, implementation, execution, control and completion of specific facilities/maintenance/calibration projects at the client site.
Initiate and lead clinical study teams as clinical director. Responsible for the successful operations of all study teams to achieve the study objectives at the highest standards and on time and budget.
The Senior Process Validation Engineer will be responsible defining, implementing, and maintaining a robust process validation program. The process validation program includes, but is not limited to, biological growth processes, aseptic processing, cleaning, and sterilization processes.
POSITION SUMMARY: To provide SAS programming support for the Clinical Research Programming Department. ESSENTIAL FUNCTIONS:1. Develop and document programs to create analysis datasets summarizing key clinical trial data. 2. Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results.
A board certified oncologist/hematologist with industry experience who will report to the Chief Medical Officer and work collaboratively with the Clinical Study Team contributing to the strategic planning and execution of Clinical Development Plans for all compounds in clinical development.
Validation Engineer - Biotech6-8 month contract intitially - $70-$100 per hour DOEThe Validation Engineer reports directly to the Manager of Validation. You will be responsible for performing validation in a GMP biotech manufacturing facility managing large size validation projects and supervising technicians/engineers as necessary.
You are checking job search results for program manager jobs in cove bay on JobiJoba UK, your search engine for jobs
