SITE LOCATIONS: CALIFORNIA: Los Angeles, San Diego, San Francisco - Candidate must live in this area, not just willing to travel to it. No relocation arrangements will be considered.
Delivery of high quality data according to agreed timelines and budget, ensuring adherence to international and local regulations and company SOP standards.
Demonstrate exceptional customer focus as evidenced by positive feedback from colleagues and external customers (Investigators).
CRAs - Join Covance and receive a $5000 Sign On Bonus!
Experienced Clinical Research Associates (CRAs)/Monitors: We are hiring Phase I-IV CRA positions.
Positions are home-based and needed throughout the United States.
All therapeutic areas needed. Please let us know your therapeutic experiences on your resume.
Focusing on balance and quality by only working on 1 to 2 studies!
Our Clinical Research Associates /CRAs / Monitors manage all aspects of site monitoring responsibilities for ...
My client is leading Japanese pharmaceutical company that has been providing innovative medicines essential to human health for 130 years. They are a unique and entrepreneurial mid-sized pharmaceutical company that develops and commercializes pharmaceutical products that address unmet medical needs, specifically in:
My client has a distinguished history in developing innovative therapies that address unmet medical needs. With its core business of ...
SITE LOCATIONS: MidWest: Chicago, Houston/Dallas, Denver, St. Louis, Kansas City
SITE LOCATIONS: Florida, North Carolina, South Carolina
SITE LOCATIONS: CALIFORNIA: Los Angeles, San Diego, San Francisco
MUST live within driving distance to airport in one of these cities.
• Delivery of high quality data according to agreed timelines and budget, ensuring adherence to international and local regulations and company SOP standards.
• Demonstrate exceptional customer focus as ...
Looking for a professional to work for an industry leader, with proven Health Policy experience in the Medical Device or Pharmaceutical Industry.
Responsibilities: Support current and future products within the diabetes portfolio from a value & access point of view and as well as a global scale. Contribute to the critical planning and execution of activities that best position Diabetes for success in light of the sweeping changes in business environment, due to ...
Precept Life Sciences is seeking experienced Regional CRAs across the country for permanent positions with several leading CROs.
On average, CRAs are assigned to an average of 12 sites across 1-3 protocols. Study and site assignment will vary depending on monitoring duration/frequency, location of sites and complexity of trial.
CRAs are expected to be 80% billable, with approx. 60% travel.
We are looking for CRAs that are not just field monitors, but those that manage all aspects of the site ...
*RELOCATION to San Francisco Bay Area/Silicon Valley Required (relocation assistance provided)*
This role will immediately assume study lead data management responsibilities for 3-5 concurrent clinical trials within Oncology, Respiratory or Liver Disease, utilizing primarily the Medidata RAVE electronic data capture and management system. The selected candidate will manage trials in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high ...
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 ...
Oct 17 -
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