Allucent

pharmaceuticals and biologics

Sr.ClinicalResearchAssociate(Germany)

Cologne, North Rhine-Westphalia, Germany FULL TIME
The Brief

“Sr. Clinical Research Associate (Germany) at Allucent. Skills: Clinical Research Associate, monitoring expertise, regulatory affairs, site activation. Independently control and monitor investigational sites. pro-actively detect issues”

Industry & Context.

pharmaceuticals and biologics
Problems you'll solve

provide solutions; Identify and resolve site issues

Eligibility Requirements

Travel throughout Germany., Willingness to travel, as required (8 DOS per month).

What They're Looking For.

Must Have

Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience., understanding of ICH-GCP and regulatory guidelines., Clear and confident communicator in English and German., Comfortable working independently and managing priorities., Willingness to travel, as required (8 DOS per month).

What You'll Do.

Independently control and monitor investigational sites

pro-actively detect issues

provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs

applicable regulations

and the principles of Good Clinical Practice

take the lead on monitoring activities

owning your sites and relationships with investigators

bridge between sponsor and site

ensuring trial integrity

Independently manage all aspects of monitoring for assigned clinical trials across study phases

including site initiation

and close-out visits.

Ensure compliance with protocols

and applicable regulatory requirements.

Build site relationships

acting as a primary point of contact and ensuring high-quality data collection.

Identify and resolve site issues

escalating as needed to maintain trial integrity and patient safety.

Activities around regulatory affairs

site activation and study-startup.

How You'll Work.

Team & Collaboration

forge meaningful partnerships with clients; collaborate with top minds across science, business, and operations; supported by a collaborative, experienced team; thrive in an agile, collaborative environment

Communication Scope

Clear and confident communicator in English and German.

Process & Methodology

Independently manage all aspects of monitoring for assigned clinical trials across study phases

Free ATS check

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