Bryan Johnston's Research Jobs
Quality Control SpecialistResearch - Woodcliff Lakes, NJ 07677
ClinForce is seeking a Quality Control Specialist in the Woodcliff Lakes, NJ area. Responsibilities will include QC of documents including protocols, protocol amendments, investigator brochures, clinical study reports, and regulatory documentation. The QC Specialist is responsible for performing accurate, precise proof- reading to include spelling, grammar, punctuation and verification of data... Tags for this job: protocol quality » View Quality Control Specialist Job - Woodcliff Lakes, NJ Medical WriterResearch - Austin, TX 78744
ClinForce is searching for a Medical Writer. Responsibilities include: - Medical Writer will research, write, and edit clinical/statistical reports and study protocols, and summarize data from clinical studies for submission to the Food and Drug Administration (FDA). -Must possess an excellent working knowledge of medical terminology and statistical concepts. Must have experience with med... Tags for this job: medical writer clinical research » View Medical Writer Job - Austin, TX Clinical Research SpecialistResearch - Rahway, NJ 07065
ClinForce is currently seeking a Clinical Research Specialist. Responsibilities will include: • Receives Serious Adverse Event information and will create, review and manage case reports for those events. • Adhere to reporting timeframes and ensure compliance with regulations. • Supports the clinical team in the medical review of reportable event data. Generate safety queries to the study ... Tags for this job: adverse event, drug safety, » View Clinical Research Specialist Job - Rahway, NJ Safety Data CoordinatorResearch - Durham, NC 27703
Responsibilities will include: -Collecting and tracking incoming Adverse Event (AE) and endpoint reports; -Determining initial/update status of incoming events; and tracking timelines for completion of events. -Assist with entering data into Safety databases, submitting event data to Operational Team members, tracking submission, and assume workflow responsibilities for assigned projects ... Tags for this job: safety data » View Safety Data Coordinator Job - Durham, NC Regulatory Affairs OfficerResearch - Kansas City, MO 64137
Responsibilities will include: • Prepares and/or reviews regulatory submissions to support clinical trial and marketing authorization activities • Function as a Regulatory Team Leader on regulatory projects • Identifies project needs, tracks project timelines, implements client requests and manages day-to-day workload in collaboration with senior staff, as appropriate. • Prepares and/or ... Tags for this job: regulatory affairs submissions |
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