Are you an organised, curious, and collaborative professional looking to advance your clinical project management career? We are seeking Associate Clinical Project Managers to join a dynamic Global Clinical Sciences & Operations team.
In this role, you will provide hands-on operational support to Clinical Project Managers, ensuring clinical studies run smoothly from protocol through to final report and archiving. You’ll help maintain study documentation, track progress, coordinate with stakeholders, and support the team in meeting timelines, quality, and regulatory requirements.
What you’ll do:
* Maintain the Trial Master File (TMF) to ensure it is audit-ready.
* Support the creation, review, and finalisation of study documents (protocols, amendments, consent forms, reports).
* Coordinate stakeholder communications, meetings, decisions, and action logs.
* Track study status, metrics, invoices, and risks; provide clear updates to the study team.
* Assist with external partner coordination, training, and readiness for audits or inspections.
* Set up and maintain study records in clinical systems, performing quality checks.
What we’re looking for:
* Bachelor’s degree (or equivalent) in a relevant scientific, health, or business discipline.
* 1–3 years’ experience in clinical research, including trial coordination or project support.
* Exposure to global matrix environments and phase 2–3 studies is a plus.
* Strong organisation, prioritisation, and attention to detail.
* Excellent English communication skills across cultures and time zones.
* Comfortable with office productivity tools and clinical study systems.
Why join us?
This is a fantastic opportunity to grow your career in clinical project management, working across multiple therapeutic areas including immunology, neurology, and rare diseases. You’ll gain hands-on experience supporting clinical studies while contributing to process improvements and team success.
Start Date: ASAP