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Clinical Research Associate (Contract Basis)

3-4 years
Not Disclosed
10 Jan. 23, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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

Job Title: Clinical Research Associate (Contract Basis)

Location: Thailand

Experience Required: 3 – 4 Years

Job Description:

We are seeking a Clinical Research Associate (CRA) to join our team on a contract basis. The ideal candidate will have 3 to 4 years of experience in clinical research and be responsible for ensuring the successful planning, execution, and monitoring of clinical trials in compliance with regulatory standards and protocols.

Key Responsibilities:

  • Conduct site selection, initiation, monitoring, and close-out visits for clinical trials.
  • Ensure that clinical trials are conducted in compliance with ICH-GCP, local regulatory requirements, and study protocols.
  • Review and verify source documents, case report forms (CRFs), and other study documents for accuracy and completeness.
  • Provide support to sites for patient recruitment, enrollment, and retention.
  • Maintain up-to-date knowledge of regulatory guidelines and industry standards.
  • Coordinate with study teams, investigators, and vendors to ensure timely execution of clinical trials.
  • Prepare and submit reports related to site monitoring and trial progress.
  • Identify and resolve any study-related issues or concerns in a proactive manner.

Qualifications:

  • Bachelor's degree in Life Sciences, Pharmacy, or a related field.
  • 3-4 years of experience as a Clinical Research Associate (CRA).
  • Strong knowledge of ICH-GCP and local regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and manage multiple priorities.
  • Fluent in English and Thai (both written and spoken).
  • Willingness to travel as needed for site visits.

This contract-based position offers an exciting opportunity to contribute to the advancement of clinical research in a dynamic and collaborative environment. If you meet the above qualifications and are looking for a challenging and rewarding role, we encourage you to apply.

Send your CV at career@prorelixresearch.com to explore career opportunities with ProRelix Research.