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Senior Clinical Data Coordinator


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https://www.pop-science.co.uk/1429/job2021-10-28 10:23:011970-01-01 Pop Science
Job Type Permanent Full Time
Location United Kingdom
Area EMEA (other), Rest of World EMEA (other) Rest of World United Kingdom
Sector Science
Salary £30k - 35k per year
Currency gbp
Start Date ASAP
Advertiser remoteapi
Job Ref 1177
Job Views 182
Description

Are you a Clinical Data Coordinator looking to work for a global Oncology client in London? Hybrid working model on offer.

You will ned to ensure clinical data is transcribed into Electronic Data Capture (EDC) systems accurately, timely and in accordance with company SOPs, GCP and ICH regulations and guidelines. To provide training and mentoring to the team of Clinical Data Coordinators.

Support and Management.

  • Provides mentoring and training to junior team members.
  • Provides out of office cover for the Clinical Data Lead.
  • Assists with the preparation of the end of month data status report
  • Prepares for study activation by ensuring department is ready for first patient.
  • Ensures all sponsor data deliverables are met.
  • Accurately enters clinical data into EDC systems in a timely manner.
  • Facilitates monitoring visits by establishing and building positive relationships with CRAs.
  • Completes query resolution by liaising with clinical team members when required.
  • Sends required clinical data to vendors when specified by Sponsor/CRO eg. Imaging.
  • Maintains and archives study patient source documentation.
  • Performs regular checks of source documentation and data entered into EDC systems.
  • Attends meetings as assigned and reports on actions.
  • Perform ad hoc duties/projects as directed to enhance data processes.
  • Provides support to SCRI UK finance in regards to Sponsor queries that require Data Management verifications.

Experience

  • Practical experience using clinical data management tools eg: Medidata RAVE, Inform
  • Knowledge and experience with clinical data and ICH Good Clinical Practices
  • Experience in oncology and clinical trials
  • Previous experience in a supervisory role

The post holder will have excellent organization skills, be able to accurately transcribe data, quality control check data for compliance with GCP regulations and build good relationships with external clients. In addition will be approachable for junior team members to ask questions on daily data operations tasks.

#oncology #pharmajobs #cta #datamanager

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