Browse Career Research in Research
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Finger Lakes Clinical Research
Work closely with study sponsors to ensure protocol compliance. Assist PI with the management of multiple clinical trials. Track and dispense study medications to ensure proper drug accountability.
Avg. Salary: $75,000 · Company Rank: Not Available
Bausch & Lomb, Inc.
Manage reporting of medical findings/adverse events to Regulatory Affairs. Assure compliance with FDA regulations, ICH, and GCP guidelines. Monitored clinical sites involved with testing of investigational devises.
Avg. Salary: $75,000 · Company Rank: Not Available
Bausch & Lomb, Inc.
Prepare submissions/applications to gain market approval/clearance. Participation on product development teams. Review of all labeling, advertising and promotional material for ophthalmic solutions to ensure compliance with US and International regulations.
Avg. Salary: $75,000 · Company Rank: Not Available
Manchester University
Research Associate: In the collaboration, I am responsible to the theoretically analyse and computer programming using of Mathematica software. The main topic is about the band structure and electronic transport properties of graphene-based two-dimensional material, superlattice-related effect on graphene in magnetic field. All those results are published in high-level academic journals.
Avg. Salary: $30,000 · Company Rank: Not Available
The Clinical Research Center, Inc,
• Assist in the identification of potential study sites • Identify/select investigators who will be responsible for the conduct of the trial • Set up the trial sites, which includes ensuring each center has the trial materials, including the investigational medicinal product • Monitor trials throughout their duration by conducting various Site Monitoring visits (including PSVs, SIVs, IMVs and COVs) to meet study expectation...
Avg. Salary: $125,000 · Company Rank: Not Available
The Clinical Research Center, Inc
• Identify/ select investigators who will be responsible for the conduct of the trial • Set up the trial sites, which includes ensuring each center has the trial materials, including the investigational medicinal product • Review CRF's, data management plans, study reports, and informed consents • Conduct source data/document verification (SDV) • Monitor trials throughout their duration by conducting various Site Monitoring...
Avg. Salary: $125,000 · Company Rank: Not Available
The Clinical Research Center, Inc
• Processing of information received from pharmaceutical sponsors and clinical research organizations • Development of source files and regulatory documents • Conduct subject visits, including scheduling, delivery of oral and written informed consent, charting, medical testing (e.g., vital signs), and processing of data and samples collected during subject visits • Subject recruitment and screening & Subject database manag...
Avg. Salary: $125,000 · Company Rank: Not Available
Fluid-Screen, Inc.
-Culturing bacteria and fungal strains -Testing prototype devices -Interacting with customers -Testing client samples -Writing research proposals and reports -Writing IBC amendments -Establish collaborations
Avg. Salary: $94,000 · Company Rank: Not Available
Brown University
Avg. Salary: $94,000 · Company Rank: Not Available
University of Massachusetts Medical School
Avg. Salary: $94,000 · Company Rank: Not Available