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Job Summary

The Clinical Research Associate plays a pivotal role in ensuring the rights and wellbeing of trial participants are safeguarded.

Key Responsibilities:

  • Establish and maintain site relationships to guarantee trials adhere to ICH GCP guidelines, local and global regulatory requirements, and Standard Operating Procedures (SOPs).
  • Cultivate strong working relationships with Principal Investigators, study coordinators, pharmacists, and site trial personnel to ensure seamless clinical trial management.
  • Collaborate with internal teams to provide project support as per study demands and timelines.

Requirements:

  • Hold a degree in a clinical or life sciences-related field.
  • Demonstrate good time management, attention to detail, ability to work effectively within a team, and proficiency in computer applications.
  • Experience by job level: CRA II – minimum 6 months of independent monitoring experience; CRA III – 2+ years; SCRA – minimum 4 years of CRA monitoring experience.