$5000 Hiring Incentive for Qualified Candidates!
Covance is seeking Clinical Research Associates / CRA / Monitors with cardiovascular / coronary artery disease therapeutic experience for a special hypercholesterolaemia project.
Positions are home-based and urgently needed in the following locations: Raleigh, Dallas, Boston, Chicago, Minneapolis, NYC, Florida, and California.
Our Clinical Research Associates /CRAs / Monitors manage all aspects of site monitoring responsibilities for ...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.
Title: Project Manager III
Job ID: 21911
Location: Thousand Oaks, CA
Duration: 12 Month Contract
Pay Rate Range: Depends on Experience (W-2 all inclusive rate)
Resource allocation and all phases of development life cycle (i.e. ...
This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor:
· Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects
· Conduct Pre-Study Site Visits (or calls), ...
We are currently looking to hire Permanent Senior Regional CRA's
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, ...
If you are a CRA or a Senior CRA we’d like to speak with you!
We currently have a number of different clients looking for CRAs and SCRAs. They each have different perks, options and ways of doing business that make them very appealing. These are all permanent positions, however, if you have a contract background and are looking to make a switch, that will not disqualify you from any of these roles. Salaries are based on experience, current compensation and market conditions and range from $75K- ...
Title: Clinical Project Manager
Company: Medical Device Company
Location: Orange County, CA
Status: Permanent Placement, 40 hours/week
• Clinical Project Manager manages U.S. field activities for the conduct of clinical research studies in compliance with applicable regulatory standards, IRB/EC policies and procedures and company policies and procedures. This position works with minimal supervision in consort with study management. This ...
The Principal Scientist will be the PKDM Development Project Team Representative on the Early and/or Global Development Teams in the area of Oncology. He/she will support small and large molecule drug development, registration, and post-marketing activities. He/she will be responsible for program-level strategic and resource planning, communication, scientific/technical deliverables, issue resolution, and functional representation for internal governance reviews, face-to-face interactions with global ...
Seeking at least 5 years experience designing, developing, and validating molecular diagnostic assays for CLIA approved tests.
*** Assay process development, documentation, and scale up experience.
*** Developed DNA array based molecular assays for diagnostics.
*** MS or PhD degree.
Starting salary up to $110,000 plus comprehensive benefit packages and the opportunity to collaborate with top scientific personnel on a daily basis. If you are ready to make a difference, do not ...
Apr 11 -
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