Clinical Research Associate

ProClinical is currently recruiting for a Clinical Research Associate job in Thailand. This is a large organisation focused on finding solutions for serious unmet medical needs, this is a great place to excel in your clinical career. There is an opportunity to work from home, if you are needed.

Job Responsibilities

• Responsible for evaluation, initiation, monitoring, close-out and other tasks associated with the management of clinical sites.
• Ensure the conduct of all clinical studies is in accordance with Good Clinical Practices, International Harmonization Guideline, and appropriate Standard Operating Procedures (SOP)
• Serve as primary contact for Clinical Research Organizations/ vendors, Investigators and study coordinators for study related questions.
• In conjunction with study team, support feasibility and site selection process for clinical studies.
• Manage patient recruitment strategies to increase patient randomization into the trial
• Review all Adverse Events/Serious Adverse Events and ensure appropriate documentation is in place and any other safety issues are addressed and communicated.
• Order and coordinate study supplies for clinical studies
• Develop and maintain tracking tools to support management of clinical studies

Skills and Requirements

• Bachelor or nurse degree, preferably in the Life Sciences
• Minimum of 3+ years of experience in the pharmaceutical / biotechnology industry or CRO as a Clinical Research Associate from study start-up to database lock.
• Strong Oncology monitoring experience in phase 1-3 pharmaceutical/ biotechnology clinical trials
• Strong working knowledge of Electronic Data Capture, Interactive Voice/Web Response System and
  Clinical Trial Management System
• Fluent in Danish and English, oral and written
  

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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