Senior CRA

Hobson Prior; Dortmund; Vor Ort; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Senior Clinical Research Associate to lead groundbreaking clinical research efforts. In this pivotal role, you will independently manage and monitor clinical trial sites, ensuring compliance and quality standards are met. You will collaborate with diverse teams to support trial execution and tackle site-related challenges. This position offers the opportunity to make a significant impact in the life sciences sector, providing a platform for your expertise and leadership skills. If you are passionate about advancing clinical research and thrive in a dynamic environment, this role is perfect for you.

Qualifikationen

• Degree in life sciences or related field required.
• Experience in clinical monitoring within the pharmaceutical or biotechnology industry.

Aufgaben

• Guide the clinical research team to ensure projects stay on track.
• Conduct site visits to ensure proper documentation and compliance.
• Train and mentor new team members.

Kenntnisse

Clinical Monitoring

Attention to Detail

Organizational Skills

Communication Skills

Problem Solving

Ausbildung

Degree in Life Sciences

Tools

Clinical Trial Management Systems

Jobbeschreibung

Are you looking to drive groundbreaking clinical research and make a real impact? This position as a Senior CRA is your next step to lead the way in advancing clinical research!

Hobson Prior is seeking a Senior Clinical Research Associate to join our team. In this role, you will independently manage and monitor clinical trial sites, ensuring they meet quality and compliance standards. You will work closely with various teams to support trial execution and address any site-related issues.

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 ensure projects stay on track.
• Review reports from site visits and conduct evaluations as needed.
• Ensure timely visits to trial sites and resolve any issues that arise.
• Help develop plans and training materials for monitoring studies.
• Manage study budgets and provide financial information as required.
• Conduct site visits to ensure proper documentation and compliance.
• Maintain regular communication with trial sites to ensure adherence to protocols.
• Facilitate reporting of adverse events and resolve data discrepancies.
• Train and mentor new team members.

Key Skills and Requirements :

• Degree in life sciences or related field.
• Experience in clinical monitoring within the pharmaceutical or biotechnology industry.
• Strong attention to detail and organizational skills.
• Ability to manage multiple tasks and solve problems effectively.
• Excellent communication and interpersonal skills.
• Proficiency in using clinical trial management systems and databases.
• Knowledge of clinical research guidelines and regulations.
• Ability to travel as needed.

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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