Global Clinical Development Specialist

hace 1 día


Madrid, Madrid, España Tfs Healthscience A tiempo completo

About Tfs Healthscience We are a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. The role of the Global Clinical Development Specialist is part of Strategic Resourcing Solutions (SRS) within Tfs Health Science and will function operationally as a member of a Project Team and is responsible for the initiation, on-site and/or remote monitoring, close out of study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements Key Responsibilities

  • Monitor on-site and remotely clinical trials in accordance with Tfs and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations.
  • Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality.
  • Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations.
  • Review CRFs (electronic or paper) and subject source documentation for validity and accuracy Verify proper management and accountability of Investigational Product.
  • Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required escalate observed deficiencies and issues as appropriate.
  • Providing site with the listing of issues identified during monitoring visit and action items which will need to be addressed in a timely manner.
  • Timely delivering site documents to eTMF or paper TMF verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and ICH guidelines and local regulatory requirements.
  • Participate in audit and/or inspection, its preparation and follow-up activities, as needed.
  • Order, ship, and reconcile clinical investigative supplies for study sites, if applicable Update CTMS and all other required by projects systems with accurate site level information
What You'll Get
  • A competitive annual salary of $65,000-$80,000 based on experience.
  • Comprehensive benefits package including health insurance, retirement plan, and paid time off.
  • The opportunity to work in a fast-paced environment with changing priorities.
Requirements
  • Bachelor's Degree, preferably in life science or nursing or equivalent.
  • Over 4-5 year of relevant clinical experience or relevant academic background around clinical trial or clinical development activities.
  • Able to work in a fast-paced environment with changing priorities.


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