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Clinical Trial Assistant

0-3 years
Not Disclosed
15 June 20, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About the job

The brief job description as below:

  • To administer, maintain and coordinate the logistical aspects of the clinical trials according to GCP and SOPs

  • Work side-by-side with CRA and assisting in some of their tasks

  • Prepare and maintenance of the various documents and CRFs for the study

  • Perform liaison activities with the Independent Ethics Committees

  • Be the central contact and support between the contract laboratory, study team and study site

  • Provide logistical support for the clinical trial

  • Provide agenda, minutes and action points for meetings

  • Assist in managing the site budget activities

  • Provide administration support to the management

 

Qualifications, Experience & Skills:

  • Research or health care related academic or work experience preferable

  • Good organizational skills, ability to manage multiple tasks and meticulous attention to detail

  • Good written and verbal communication skills

  • Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook