Start-Up Associate II (Italy)

Allucent

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Role summary

Allucent seeks a Start-Up Associate II to coordinate clinical trial site initiation activities in Italy. The role involves managing regulatory submissions, ethics committee interactions, contract negotiations, and essential document collection for biopharmaceutical studies across hybrid and remote settings.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workable, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Life science degree or equivalent qualification in related allied health profession
Experience coordinating clinical trial regulatory and ethics submissions
Proficiency with clinical trial management systems and electronic trial master files
Knowledge of local and international clinical trial regulations and guidelines
Strong communication skills with regulatory authorities and ethics committees
Contract negotiation and management experience in clinical trial context

What you'll be doing

Track start-up activities, milestones, and progress in CTMS and associated systems
Prepare, compile, and submit regulatory and ethics documentation to relevant authorities
Coordinate responses to regulatory authority and IEC/IRB inquiries and questions
Negotiate, review, and finalize clinical trial agreements and site contracts within approved parameters
Collect and manage essential documents from investigator sites with quality review

Privacy & handoff

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What RoleLantern checked

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RoleLantern checked active

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Date posted1 day ago

Last source checkToday

Salary listedNeeds clarity

Location clearNeeds clarity

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