Clinical Research Associate II and Senior Clinical Research Associate

Overview

ClinChoice is a global contract research organization expanding its CRA network in Germany. We are seeking Clinical Research Associates (CRAs II and Senior CRA) to partner with world-leading pharmaceutical companies in biomedicine.

As a CRA, you will manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.

Responsibilities

• Manage clinical study activities across multiple sites within one or more projects, focusing on medical devices.
• Oversee site performance and conduct company-initiated clinical studies.
• Ensure high-quality deliverables through site visits, monitoring, and effective communication.

Key Requirements

• Willingness to travel to sites and surrounding countries (50-80% travel).
• Fluent in German is required.
• Prior experience in monitoring clinical trials and site management.

Skills and Qualifications

• Bachelor\’s Degree or equivalent in scientific and/or medical or paramedical disciplines; nursing or relevant degree preferred. Equivalency may be considered in some cases.
• Up to 8 years of experience as a CRA.
• Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and applicable regulatory requirements.
• Sound knowledge of medical terminology.
• Fluent in English and local language(s).
• Proficiency in Microsoft Office (Word, Excel, Outlook).

Education and Experience

• A Bachelor Degree is required, preferably in Life Science, Physical Science, Nursing, Biological Science, or related fields; Masters or advanced degrees (e.g., PhD/MD/PharmD) are a plus.
• At least 4+ years of onsite monitoring experience is required.
• Previous medical device monitoring experience is required. Therapeutic area experience in neuro- or cardiovascular domains is also required.
• Understanding and application of regulations and standards in clinical research and medical devices/combination products.
• Relevant industry certifications preferred (e.g., CCRA, RAC, CDE).
• Clinical/medical background is a plus.
• Languages: English and German proficiency; ability to monitor documentation and processes in both languages.
• Ability to travel up to 80%.

Application Process

Once you have submitted your CV, you will receive an acknowledgement. If you meet the requirements, you will be invited for a phone interview as the first step. Due to the volume of applications, we may not reply individually to everyone who is not successful.

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of experience and more than 4,000 professionals in over 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. We value our employees and invest in ongoing training to maintain high qualifications and enable effective collaboration with clients while maintaining core processes. ClinChoice is an equal opportunity employer, valuing diversity and inclusivity across gender, race, beliefs, and ethnicities.

Keywords: Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management, Monitor, Monitoring, Complex Trials, Medical Devices, Cardiology, Neurology, Open to Travel, Submissions, Ethics, Contract Research Organisation, CRO

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