Senior Clinical Data Analyst -Medical Devices & Diagnostics

Description

• You will be permanently employed by Labcorp Drug Development working in our Medical Devices & Diagnostics division working across multiple Sponsors.
  
• Office based or home based anywhere within the defined locations.
  
• You must have previous experience of working in a clinical data management role, any experience within Medical Devices would be advantageous.
  
• Candidates must be fluent in English language (both verbal and written).
  

Join our growing team and discover your extraordinary potential by working as a Senior Clinical Data Analyst within our Global Clinical Development department. This is a great opportunity for a Clinical Data Analyst who wants to advance their Data Management career, working closely with the Data Managers. You will be responsible for a variety of tasks across, data review, database validations & query management.

You will be a key member of team and assist Data Managers working across a variety of global studies. This is an excellent chance to broaden your experience across Clinical Data Management and gain end to end exposure across study start up, maintenance and database lock.

Duties will include:

• Serve as a member of the project team with primary responsibility for coordinating the clinical data review, query generation / resolution and reconciliation activities to support the Data Management lead with the delivery of clinical data according to client quality and integrity specifications, project timelines and productivity targets.
  
• Assist in the development of the project Data Management Plan, including data review guidelines /diagnostics specification and setup of the data management systems according to project requirements.
  
• Assist with reviewing clinical trial data in accordance with Data Management Plans, Edit Check Specifications and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data.
  
• Generate, resolve and track queries to address problematic data identified during aggregate data review activities.
  
• Run and execute additional programs, special listings, reconciliation discrepancy listings etc.) used to support the review of clinical trial data.
  
• Assist with review of data listings for internal data review.
  
• Assist or create dummy data to test edit checks and to test database screen design and functionality.
  
• Assist or create dummy data to test SAS reports and data listing.
  
• Modify standard templates to create study specific Data Management Plans, or eCRF completion guidelines.
  
• Posting of Data Management documentation and data management related administrative tasks as requested, including maintenance of eTMF as required.
  
• Generate study status reports.
  
• Perform database extracts.
  
• Assist with the completion of Database Lock activities.
  
• Support the training of new staff on project
  

Education

• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
  
• Additional relevant work experience will be considered in lieu of formal qualifications.
  

Experience

• Applicable experience in clinical research (Data management preferred).
  
• Knowledge of medical terminology.
  
• Demonstrate time management skills and ability to adhere to project productivity metrics and timelines.
  
• Demonstrate ability to work in a team environment and collaborate with peers.
  
• Demonstrate good organizational ability, communication and interpersonal skills.
  
• Demonstrate team working and good collaboration skills.
  
• Knowledge of drug development process.
  
• Knowledge of effective clinical data management practices.
  

Keywords:

Labcorp Drug Development, Covance by Labcorp, CRO, Contract Research Organisation, Contract Research Organization, pharma, pharmaceutical, clinical data management, Clinical Data Management, Diagnostics, Medical Devices, Clinical Data Management, home based, pharma, home-based, flexible working, flexible location, field based, field-based, United Kingdom, UK, Great Britain, England, Maidenhead, Reading, Berkshire, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Austria, Bulgaria, Czech Republic, Greece, Hungary, Lithuania, Poland, Romania, Russia, Slovakia, Bloemfontein, Centurion, South Africa, #LI-Remote, Remote, EMEA

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