Senior Clinical Research Associate

Hobson Prior; München; Remote; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading life sciences recruiter is seeking a Senior Clinical Research Associate to oversee and conduct site monitoring activities for clinical trials in Germany. The ideal candidate will have a background in life sciences, experience in clinical monitoring, and excellent communication skills. This role is fully remote and requires the ability to manage multiple tasks while ensuring compliance with protocols and regulations. Strong attention to detail and proficiency in English are essential.

Qualifikationen

• Experience in clinical monitoring within the pharmaceutical, biotechnology, or CRO industry.
• Knowledge of clinical research regulations, ICH-GCP, and ethical requirements.
• Willingness to travel as required.

Aufgaben

• Guide and support the clinical research team to meet project goals and timelines.
• Conduct and document site visits, ensuring compliance.
• Collaborate with internal teams to resolve data discrepancies.

Kenntnisse

Attention to detail

Organizational skills

Communication skills

Interpersonal skills

Ability to manage multiple tasks

Proficiency in English

Ausbildung

Background in life sciences or related field

Tools

Clinical trial management systems

Electronic data capture tools

Jobbeschreibung

Overview

Hobson Prior is seeking a Senior Clinical Research Associate to join a dynamic team in Germany. This is a fully remote role, open to candidates located anywhere within Germany.

In this role, you will oversee and conduct site monitoring activities for clinical trials, ensuring compliance with protocols, regulations, and quality standards. You will also provide leadership and guidance to the clinical team while collaborating with cross-functional departments to support study execution.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities

• Guide and support the clinical research team to meet project goals and timelines.
• Conduct and document site visits, including initiation, interim, and close-out visits.
• Ensure proper documentation and compliance with study protocols and regulations.
• Review and verify data accuracy through source document checks.
• Assist with site training, recruitment, and addressing site-related issues.
• Oversee investigational product accountability and regulatory documentation.
• Collaborate with internal teams to resolve data discrepancies and ensure study progress.
• Provide mentorship and training to new team members.
• Support audit preparation and maintain compliance with ICH-GCP guidelines.

Key Skills and Requirements

• Background in life sciences or a related field.
• Experience in clinical monitoring within the pharmaceutical, biotechnology, or CRO industry.
• Strong attention to detail and organizational skills.
• Ability to manage multiple tasks and work effectively under pressure.
• Proficiency in English and the local language for the region of monitoring activities.
• Knowledge of clinical research regulations, ICH-GCP, and ethical requirements.
• Excellent communication and interpersonal skills.
• Willingness to travel as required.
• Familiarity with clinical trial management systems and electronic data capture tools.

Additional Information

For more information, please contact Elliott Croft.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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