$110K — $120K *
Remote Clinical Trial Manager needs Minimum of 3 to 5 years in the pharmaceutical industry/CRO, which includes 1-2 years of clinical/medical research experience, or transferrable skills.
Remote Clinical Trial Manager requires:
B.S. degree (life science or health related preferred).
Ø Process and system thinking, customer orientation, and ability to work in multidisciplinary study teams and to execute within a matrix management model, ideally in pharmaceuticals/biotech.
Ø Experience in execution of clinical research trials, including GCP and regulatory guideline knowledge and audit inspections.
Ø Experience in the management of CROs and other clinical trial related vendors.
Ø Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics.
Ø Demonstrated ability to support the development and management of various aspects of the end to end study operational plan.
Ø Demonstrated ability to support the operational execution and delivery of various aspects of a quality clinical trial.
Ø Program and project management experience preferred
Ø Experience in leading and managing interventional, observational, prospective, retrospective trials and/or chart review studies.
Ø Migraine and/or Aesthetics experience a plus
Ø International experience a plus.
Ø Knowledge of drug development and FDA GCP/ICH regulatory guidelines.
Ø Proficiency with and ability to utilize software applications that support Clinical Operations: Microsoft Word, Excel, PowerPoint; Adobe Acrobat, EDC systems, etc.
Ø Clinical trial management system (CTMS) background is a plus.
Remote Clinical Trial Manager duties:
Ø Responsible for the execution and adherence of various aspects of the study operational plan (start up, conduct, close-out, and vendor oversight) with input from key stakeholders including adherence to all relevant regulations including GCP, ICH and Regulatory requirements, as well as company SOPs and policies.
Ø Responsible for managing study budget, timelines, and risk mitigation processes
Ø Responsible for managing the selection, contracting and oversight of CROs and other clinical trial related vendors in collaboration with Procurement and key stakeholders.
Ø Responsible for ensuring up-to-date trial information is entered into CTMS and other required systems.
Ø Assist as required with departmental projects and provide recommendations for continuous procedural improvements.ntinuous procedural improvements.
Valid through: 11/10/2021
$140K — $160K *
8 days ago