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Clinical Research Associate

2+ years
Not Disclosed
10 Nov. 13, 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, CPC Certified, 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

We Are Hiring: Clinical Research Associate for Clinical Trial Monitoring at Clinexel Life Sciences Pvt. Ltd.

Location: Mumbai

Essential Qualifications:

  • M Pharm/B Pharm.

Experience:

  • Minimum 2 years of experience in core clinical trial management.

Job Summary:

  • Site Feasibility/Evaluation & Initiation: Conduct site feasibility studies and initiate site activities.
  • Regulatory Compliance: Ensure all regulatory requirements are met.
  • Site Personnel Training: Provide training for site staff.
  • Logistics & Inventory Support: Ensure site receives necessary logistical and inventory support.
  • Monitoring & Data Verification: Monitor data and verify source records.
  • IP Accountability: Manage investigational product accountability.
  • Reporting: Prepare annual and monthly progress reports.
  • Study Oversight: Oversee study progress at the site level and ensure protocol compliance.
  • Regulatory Adherence: Ensure compliance with GCP/ICH guidelines and other applicable regulatory requirements.
  • Project Management Support: Assist the project management team with relevant tasks.

If you are interested, please send your CV to careers@clinexel-cro.com by 30 Nov 2024.