Bryan Johnston's Research Jobs
Research - Chicago, IL 60602
ClinForce is actively seeking a Clinical Trial Manager for the Chicago area. Responsibilities of this position will include: • Manage sponsor and key project deliverables; • Provide project support and performance management to project team members; • Direct supervision to Clinical Research Associates and Project Coordinators; • Manage contract requirements; • Manage timeline adhere...
Tags for this job: clinical trial, timelines
Research - Deerfield, IL 60015
ClinForce is currently seeking a Clinical Research Medical Writer for the Deerfield, IL area. Responsibilities will include: -Write and prepare post marketing aggregate safety documents for regulatory submission, such as Clinical Evaluation Reports (CERs), PSURs and associated documents etc. -Ensure all safety regulatory documents are processed and submitted according to regulatory requi...
Tags for this job: medical writer, pharmacovigilance, PSUR
Research - Durham, NC 27703
ClinForce is currently seeking a SOP Manager for the Durham, NC area. Responsibilities will include: Assist Director of QA with client and regulatory audits Manage all SOP writing projects including new SOPS and review of all draft and final SOP content development. Streamlining existing SOPs and development of new SOPs related to internal possesses. Ensure that all team members...
Tags for this job: quality, gcp, sop,
Research - Cincinnati, OH 45227
ClinForce is currently seeking a GCP QA Auditor for the Cincinnati, OH area. Responsibilities will include: --Coordinate, conduct, track, and resolve Sponsor audits, Regulatory Authority inspections, investigative site audits, system audits, vendor audits, and Fraud and For Cause investigations on company- wide basis --Track, and resolve Standard Operating Procedure (SOP) deviations --Co...
Tags for this job: Audit, quality assurance, GCP
Research - Durham, NC 27703
ClinForce is currently seeking a Drug Safety Administrator located in the Durham, NC area. Responsibilities will include: Administrative responsibilities for Adverse Events including create folders, enter data in the departmental Tracker and/or Adverse Event log, safety database data entry, limited data coding, quality control review and scanning activities. Provide primary administrative ...
Tags for this job: administrative, safety
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geography, Manager, Marketing, Advocate, Survey Research, Principal Investigator, GIS, Mechanical, Developement, Innovation
Teacher for several years, Specialties: Research, Computational Biology, Biochemistry, Chemistry, DNA Synthesis, Chromatography, HPLC, PCR, Gel elctrophoresis, UV-Vis Spectroscopy, Purification, NMR DATA collection, NMR DATA processing, NMR DATA analysis, Development of microcontroller firmware, Exceptional liason with customers, Immunocytochemistry, Oral presentation: Scientific, Research by Creativity, a) With the C like programming of the data step in SAS, merging of two or more data sets, using elementary set theory operators like “and”, “or”, “equal”, “not” and “if-then” has been done routinely. Arrays and do loops have been u, business development, FDA
The Foundation Series , What Do You Care What Other People Think?", fda.gov, Nudge, The Plague, Flow and Transport in Porous Media and Fractured Rock, The Happiness Hypothesis: Finding Modern Truth in Ancient Wisdom, Brain Neurotransmitters, Beyond Growth: The Economics of Sustainable Developmet, Making Globalization Work