Senior Clinical Research Associate

4 days ago

Adelaide, South Australia beBeeClinicalResearch Full time $75,000 - $98,000
Job Overview

We are seeking a skilled Clinical Research Associate II to join our team on a sponsor dedicated basis.

The successful candidate will be responsible for conducting on-site and remote monitoring of clinical research studies, ensuring compliance with widely accepted clinical practices.

You will develop and implement tools, procedures, and processes to ensure quality monitoring, and contribute to the design, implementation, and delivery of processes, programs, and policies.

This is an excellent opportunity for those passionate about changing lives through clinical research.

About the Role:

  • Conduct site initiation visits, interim monitoring visits, and close-out visits to ensure compliance with GCP guidelines and regulatory requirements.
  • Develop and maintain effective working relationships with site staff, monitors, and other stakeholders.
  • Collaborate with cross-functional teams to support clinical trial operations and ensure seamless delivery.
  • Manage defined components of projects or processes within the area of responsibility.

Qualifications:

  • Bachelor's degree in a related field or equivalent experience.
  • Minimum of 2-4 years of experience in clinical research monitoring.
  • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and manage multiple priorities.
  • Proficiency in using clinical trial management systems and other relevant software.

Necessary Skills:

  • Attention to detail and strong analytical skills.
  • Problem-solving abilities and critical thinking.
  • Ability to work effectively in a team environment.
  • Strong organizational and time management skills.
  • Proficiency in Microsoft Office Suite.

Benefits:

  • Career development and progression opportunities.
  • Total Self culture – where you can authentically be yourself.
  • Diverse and inclusive work environment.
  • Opportunities for professional growth and advancement.
Responsibilities
  • Manage defined components of projects or processes within the area of responsibility.
  • Ensure accurate and timely documentation of monitoring activities and findings.
  • Collaborate with cross-functional teams to support clinical trial operations.
Skills and Qualifications
  • Bachelor's degree in a related field or equivalent experience.
  • Minimum of 2-4 years of experience in clinical research monitoring.
  • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and manage multiple priorities.
  • Proficiency in using clinical trial management systems and other relevant software.

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