Clinical Research Associate II

Overview

Avania is seeking an experienced Clinical Research Associate II to play a vital role in establishing, maintaining, and supporting clinical trials, primarily across Germany and the Netherlands. The CRA II will ensure the protection of participants' rights and well-being, while verifying the integrity and accuracy of trial data according to approved protocols and applicable regulatory standards such as ISO14155 or ICH-GCP.

Key Responsibilities

• Perform diverse site visits mainly focusing on monitoring activities across assigned clinical trials.
• Support various stages of the study lifecycle including feasibility assessments, site initiation, and study closeout visits as required.
• Manage responsibilities spanning multiple active protocols and sites simultaneously.
• Frequently travel to clinical sites to fulfill monitoring needs, with workload varying based on study assignments.
• Function as a versatile CRA II contributing to operational tasks and assisting senior colleagues with site interactions to optimize resource allocation.

Candidate Profile

• Previous experience as a Clinical Research Associate at a level matching CRA II responsibilities.
• Proficiency in German language is essential to support study efforts in Germany and the Netherlands.
• A residence in the Netherlands is preferred; however, candidates based in Germany will also be considered.
• Demonstrated ability to adapt to varied site management activities and work effectively across different visit types.
• Strong organizational skills to handle multiple concurrent studies and site protocols.
• Motivation to enhance clinical operations capacity and provide valuable hands-on support to a dynamic clinical team.
• Willingness and availability to travel regularly for site visits.
• Competence in clinical trial conduct and managing multiple site relationships actively.
• Open to candidates from medical device and related therapeutic areas with relevant CRA experience.
• Professional communication skills and ability to collaborate with clinical operations managers and cross-functional teams.
• Capacity to manage up to six studies simultaneously and support multiple sites within these projects.
• Flexibility to adapt swiftly to changing study priorities and resourcing requirements.

Benefits and Opportunity

This role provides significant exposure to a multi-study clinical research environment, with opportunities to engage in a variety of site visits and collaborate closely with experienced clinical leaders. Avania values ownership and proactive involvement, offering a dynamic setting where your contributions will directly affect study success and operational coverage.