Senior CRA

Hobson Prior International Ltd; Mannheim; Vor Ort; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

A leading life sciences recruitment agency is seeking a Senior CRA to oversee clinical research studies in Mannheim, Germany. The successful candidate will serve as the primary contact for study sites, ensuring compliance with protocols and regulatory requirements. Responsibilities include training site personnel, conducting site assessments, and collaborating with cross-functional teams. Candidates should have a degree in a scientific discipline, experience in clinical research, and strong organizational skills.

Qualifikationen

• A degree in a scientific discipline or related field, or equivalent education and experience.
• Experience in clinical research, laboratory work, or study coordination is beneficial.
• Strong organizational and communication skills.
• Ability to work independently and as part of a diverse, global team.
• Familiarity with clinical trial regulations and good clinical practices.

Aufgaben

• Serve as the main point of contact for assigned study sites, providing training and technical support.
• Conduct site assessments and assist in selecting appropriate study locations.
• Ensure all necessary approvals are obtained and maintained.
• Develop and review study-related documents, such as informed consent forms and monitoring plans.
• Perform site visits to monitor study progress and ensure compliance with regulations.
• Collaborate with internal teams and external stakeholders to address challenges and deliver solutions.
• Support data collection, validation, and reporting activities.
• Maintain audit readiness and adhere to all applicable guidelines and procedures.

Jobbeschreibung

Overview

Ready to be the heartbeat of clinical research? Join our client as a Senior CRA and assist in turning innovative science into life-changing care!

Hobson Prior is seeking a Senior CRA to coordinate and oversee clinical research studies at various sites, ensuring they are conducted in line with protocols, guidelines, and regulatory requirements. You will act as the primary contact for study site personnel and collaborate with cross-functional teams to ensure the successful execution of clinical trials.

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

Responsibilities

• Serve as the main point of contact for assigned study sites, providing training and technical support.
• Conduct site assessments and assist in selecting appropriate study locations.
• Ensure all necessary approvals (e.g., ethics committees, health authorities) are obtained and maintained.
• Develop and review study-related documents, such as informed consent forms and monitoring plans.
• Perform site visits to monitor study progress and ensure compliance with regulations.
• Collaborate with internal teams and external stakeholders to address challenges and deliver solutions.
• Support data collection, validation, and reporting activities.
• Maintain audit readiness and adhere to all applicable guidelines and procedures.

Key Skills and Requirements

• A degree in a scientific discipline or related field, or equivalent education and experience.
• Experience in clinical research, laboratory work, or study coordination is beneficial.
• Strong organizational and communication skills.
• Ability to work independently and as part of a diverse, global team.
• Familiarity with clinical trial regulations and good clinical practices.

Application 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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