Join the Adjutor Team as a Clinical Trial Associate (CTA)

Adjutor is seeking a Clinical Trial Associate (CTA) to support delivery of clinical trials across a range of therapeutic areas. This is an excellent opportunity to gain hands-on experience in a fast-growing global consulting environment.

Job Title: Clinical Trial Associate (CTA)

Location: Australia (Remote)

Job Type: Part Time (30 Hours/wk with potential for Full Time)

Department: Operations

Reports to: Head of Clinical

Start Date: ASAP

The Role: Clinical trial Associate (CTA)

We are seeking a Clinical Trial Associate (CTA) to support delivery of clinical trials across a range of therapeutic areas. This is an excellent opportunity to gain hands-on experience in a fast-growing global consulting environment.

Closing Date: 15th May 2026:

Applicants will be interviewed from now until 15th May and applications may close early if a suitable candidate is identified.

Join us at Adjutor—where your expertise drives business success.

Ready to Make an Impact?

Please submit your resume and a brief covering letter detailing your experience and expertise, against the selection criteria, to Annabelle Makin via the application link below.

We look forward to welcoming you aboard!

Apply Today →

About Us:

The Adjutor Group is a global consulting organisation supporting the development, regulatory approval and commercialisation of medicines and medical devices across Australia, New Zealand and international markets. Adjutor Clinical is currently recruiting additional support for their growing clinical team, and global clinical programs.

Visit us at www.adjutor.com.au to learn more about who we are!  

Why Join Adjutor?

  • Remote Flexibility: Work from anywhere with a friendly, collegial, supportive and communicative team.
  • Work-Life Balance: Flexible working arrangements.
  • Competitive Salary: Industry benchmark-level compensation.
  • Growth Opportunities: Ongoing training, mentoring & career development.
  • Innovative Environment: Share your ideas for improvement and efficiency—we’re all ears!
  • Compliance-Driven Approach: Be part of a team that values ethics, accuracy, regulatory adherence, and best practice.

Key Responsiblities of the Role

  • Maintain clinical trial documentation and trackers
  • Support TMF reviews and reconciliation
  • Organise meetings and minutes
  • Support investigational product tracking
  • Manage eTMF in compliance with ICH GCP
  • Coordinate communication with study teams and sites
  • Track sponsor oversight and study activities
  • Support importer of record activities

What You Bring: Qualifications / Experience / Skills

  • Degree in Life Sciences
  • Knowledge of ICH GCP
  • Strong organisation and communication skills
  • 1+ years clinical trial experience
  • Experience with CTMS/EDC/eTMF systems
Adjutor Head of Clinical Kim Mitchell is an experienced clinical operations Leader with a demonstrated history of working in the Pharmaceutical & Biotechnology industries.

Still have questions?

Interested in further information? Let’s have a chat!

Contact Me →