Clinical Trial Associate

Clinical Trial Associate

TFS

Søborg, Denmark

DESCRIPTION

The Clinical Trial Associate (CTA) is part of the Clinical Operations or Strategic Resourcing Solutions Unit within TFS Develop and will work, when delegated, as a member of the study team with the responsibility to organize and maintain the Study Master File (SMF) and coordinate practical tasks during the study according to company policies, SOPs and regulatory requirements.

Key responsibilities:

  • Work with the Study Team in initiating, maintaining and closing/final archiving of the SMF, ensuring GCP compliance;
  • Set up and maintenance of study information in Clinical Trial Management System (CTMS);
  • as per delegation from PM/Lead CRA or CRA;
  • Maintenance of electronic files;
  • Set up the Investigator’s File as directed by the CRA;
  • Point of contact regarding SMF;
  • Maintain the SMF as directed by the Lead CRA/Project Manager;
  • Coordinate study supplies as directed by the CRA;
  • Drafts and/or assists with the preparation of trial-related documents, tools and templates;
  • Assist in status reporting;
  • Arrange internal and external meetings;
  • Actively taking part in Study Team meetings and be responsible for the minutes;
  • Prepare, contribute to and distribute presentation material for meetings and newsletter;
  • Assist in activities associated with audits and regulatory inspections;
  • SMF completion and preparation of shipment to sponsor as directed by the Lead CRA/CRA;
  • Collection of appendices for final Clinical Study report;
  • Actively contribute to the organization and development of routines to enhance the work at TFS;
  • Work with the Study Team in all regulatory process (IEC/IRBs/CA ) including submission and amendments, regulatory fees;
  • Assist the CRA, PM or Lead CRA managing contracts with sites, including contract status;
  • To manage Investigator Payments as directed by PL or Lead CRA;
  • Assist the PL with document translations process;
  • May support the CRAs with some monitoring remote activities: collection of documentation, follow up on data entry, queries resolution.

REQUIREMENTS

  • Bachelor’s Degree preferred;
  • Knowledge of GCP/ICH guidelines;
  • Excellent written and communication skills in English and Danish;
  • Good organizational skills;
  • Good software and computer skills;
  • Able to work in a fast paced environment with changing priorities.

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© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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