Clinical Research Associate (Contractor)

Allucent

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Role summary

Allucent seeks an experienced Clinical Research Associate to independently monitor oncology trials, manage site relationships, and ensure protocol compliance. This remote contractor position (0.5 FTE, 6 months) involves site initiation, routine monitoring, and closeout activities with required travel.

What they're looking for

3-5 years of experience leading monitoring activities in complex clinical trials
Experience in complex therapeutic areas such as cell and gene therapy or radiopharmaceutical
Strong understanding of ICH-GCP and regulatory guidelines
Fluent in Hungarian and English, clear communicator
Demonstrated ability to work independently and manage competing priorities
Mastery of all clinical monitoring visit types

What you'll be doing

Independently manage all monitoring aspects including site initiation, routine visits, and closeout activities
Ensure protocol adherence, GCP compliance, and regulatory requirement fulfillment
Develop and maintain strong investigator relationships as primary site contact
Identify site issues, implement solutions, and escalate concerns to maintain trial integrity

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Date posted10 days ago

Last source check1 day ago

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