Clinical Trial Assistant
Pubblicato il 04-10-2026 - Planet Pharma in Bardi
Are you a talented Clinical Trial Assistant with a passion for clinical research?
We're looking for an experienced
Freelance CTA
to join a dynamic team supporting cutting-edge studies
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Key Responsibilities:
Assist in the
management and oversight
of clinical trials across various therapeutic areas, including
ophthalmology
,
neurology
, and
rare diseases
.
Support
Clinical Research Associates (CRAs)
and
Regulatory and Start-Up Specialists (RSU)
with study documentation, site compliance, and study performance tracking.
Prepare, distribute, and archive
clinical trial documentation
in line with standard operating procedures.
Assist in the
preparation and maintenance
of clinical trial supplies, site communications, and regulatory submissions.
Review study files for
completeness and accuracy
,
ensuring compliance with study protocols and good clinical practice (GCP).
What We're Looking For:
5+ years
of experience as a Clinical Trial Assistant (CTA) or similar role within
CRO
or
pharmaceutical
environments.
Hands-on experience supporting
global clinical project teams
and understanding of clinical trial operations.
Strong knowledge of
clinical trial systems
like
eTMF
and
Veeva Vault
(or similar).
A background in
ophthalmology
,
neurology
, or
rare disease studies
is preferred but not essential.
Ability to work
full-time
on a
12-month contract
.
Must be able to work
onsite in Milan
at least
3 days per week
.
xysqume
Fluency in English
(B2 level or higher), with strong written and verbal communication skills.
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