Senior CRA

Hobson Prior; Deutschland; Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

An established industry player is on the lookout for a Senior Clinical Research Associate to lead the charge in advancing clinical research. This pivotal role involves independently managing and monitoring clinical trial sites while ensuring compliance with quality standards. You will collaborate with various teams to support trial execution and tackle site-related challenges. If you possess a degree in life sciences and have a strong background in clinical monitoring, this is your chance to make a significant impact in the field. Join a dynamic team dedicated to driving groundbreaking clinical research and enhancing patient outcomes.

Qualifikationen

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

Aufgaben

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

Kenntnisse

Attention to detail

Organizational skills

Problem-solving

Communication skills

Interpersonal skills

Clinical monitoring experience

Ability to manage multiple tasks

Knowledge of clinical research guidelines

Ausbildung

Degree in life sciences

Tools

Clinical trial management systems

Databases

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:

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

Key Skills and Requirements:

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