Lead RF engineering solutions for aerospace and defense customers, designing test architectures and validating RF systems.
Compensation
The salary range for this role is 43,100 - 80,100 EUR gross annually, commensurate with the skills, talent, capabilities, and experience each candidate brings to a role.
Responsibilities
Understand customer RF test and validation needs and translate them into effective test architectures.
Design and demonstrate RF and microwave solutions for functional test, parametric characterization and system-level validation.
Develop proof-of-concept systems combining RF instrumentation, automation software and, where relevant, SDR and real-time signal processing.
Support projects from early technical discussions and architecture definition through evaluation, validation and deployment.
Collaborate on strategic customer engagements, capture application insights for Product and R&D, and create reusable demonstrations, application notes and technical content.
Requirements
Bachelor's or Master's degree in RF, Telecommunications, Electronics, Electrical Engineering or a related discipline.
Experienced Clinical Research Associate to manage clinical trial sites across Germany, ensuring studies are conducted in compliance with protocol, ICH-GCP, regulations, and SOPs.
Responsibilities
Perform site monitoring activities (on-site and remote) using a risk-based monitoring approach
Ensure protocol, ICH-GCP, regulatory, and SOP compliance at investigator sites
Conduct SDR, SDV, CRF review, and investigational product accountability
Identify, document, escalate, and follow up on issues through resolution, applying root cause analysis and CAPA principles
Maintain audit and inspection readiness at all assigned sites
Requirements
Bachelor’s degree in a life sciences related field or equivalent qualification
Join Us as a Clinical Research Associate to coordinate all aspects of the clinical monitoring and site management process, ensuring trials are conducted in accordance with protocol, ICH-GCP guidelines, and regulations.
Responsibilities
Monitors investigator sites with a risk-based monitoring approach
Applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure
Ensures data accuracy through SDR, SDV and CRF review
Assess investigational product through physical inventory and records review
Documents observations in reports and letters in a timely manner
Requirements
Bachelor's degree in a life sciences related field
Senior Clinical Research Associate responsible for monitoring clinical trials, ensuring compliance with ICH GCP, managing site visits, and coordinating with investigators and project teams.
Responsibilities
Monitors investigator sites using risk-based monitoring
Ensures data accuracy through SDR, SDV and CRF review
Documents observations in reports and letters
Escalates deficiencies to clinical management
Maintains contact with investigative sites
Requirements
Bachelor's degree in a life sciences related field or equivalent
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