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• Clinical Data Coordinator Dublin

• 
  Marco Tillmanns    Premium Member

  The company name is only visible to registered members.

  Clinical Data Coordinator Dublin

  Clinical Data Coordinator
  
  Role Responsibility
  Working within a highly qualified team you will perform data management activities to ensure the generation of accurate, complete, and consistent clinical databases. Fulfilling your job responsibilities in accordance with Good Clinical Practices (GCPs), using Standard Operating Procedures (SOPs), Working Procedures (WPs), Study Specific Procedures (SSPs), International Committee on Harmonization (ICH) Guidelines, and all applicable laws and regulations.
  
  Additional Responsibilities:
  • Working independently and proactively you will Review Case Report Form (CRF) data for completeness, accuracy, and consistency identifying and resolving data discrepancies
  • Update/correct/review data in the clinical databases based on resolved data queries
  • Assist with the testing of data entry screens and the preparation of the relevant testing documentation.
  • Create and maintain study files and other appropriate study documentation
  • Dependent on level of experience you may assist in training and mentoring less experienced CDC’s.
  
  Experience and Qualification
  With a University degree in medicine, science, or equivalent, you will have previous Data Management experience (for all roles above Entry Level). In addition, you will also require:
  • Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data
  • Fluency in English - Computer literate with Microsoft Office
  • Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
  • Ability to produce accurate work to tight deadlines within a pressurised environment
  
  contact:
  
  Marco Tillmanns, International Recruiter
  Telefon: +49 (0)2407/5 53 98 44
  Mobil: + 49 (0) 1520/8514525
  E-Mail: marcotillmanns@euwu.eu
  
  • 02 Aug 2011, 5:02 pm
  Marco Tillmanns wrote: > Clinical Data Coordinator > > Role Responsibility > Working within a highly qualified team you will perform data > management activities to ensure the generation of accurate, complete, > and consistent clinical databases. Fulfilling your job > responsibilities in accordance with Good Clinical Practices (GCPs), > using Standard Operating Procedures (SOPs), Working Procedures > (WPs), Study Specific Procedures (SSPs), International Committee on > Harmonization (ICH) Guidelines, and all applicable laws and > regulations. > > Additional Responsibilities: > • Working independently and proactively you will Review Case Report > Form (CRF) data for completeness, accuracy, and consistency > identifying and resolving data discrepancies > • Update/correct/review data in the clinical databases based on > resolved data queries > • Assist with the testing of data entry screens and the preparation > of the relevant testing documentation. > • Create and maintain study files and other appropriate study > documentation > • Dependent on level of experience you may assist in training and > mentoring less experienced CDC’s. > > Experience and Qualification > With a University degree in medicine, science, or equivalent, you > will have previous Data Management experience (for all roles above > Entry Level). In addition, you will also require: > • Knowledge of ICH GCP guidelines and expertise to review and > evaluate medical data > • Fluency in English - Computer literate with Microsoft Office > • Excellent communication and interpersonal skills, both written and > verbal enabling you to deal with queries in a timely manner > • Ability to produce accurate work to tight deadlines within a > pressurised environment > > contact: > > Marco Tillmanns, International Recruiter > Telefon: +49 (0)2407/5 53 98 44 > Mobil: + 49 (0) 1520/8514525 > E-Mail: marcotillmanns@euwu.eu