Clinical Research Associate

ARM International; Deutschland; On-site; EUR 45,000 - 60,000; Full time

Job summary

ARM International in Germany is seeking experienced Clinical Research Associates to join the team on behalf of an industry-leading CRO. The ideal candidate has at least 1 year of independent monitoring experience and is fluent in German (C1).

The role involves nationwide site visits (5-7 per month) and strong collaboration with investigative sites to ensure data integrity and patient safety. Responsibilities include site initiation, monitoring, and close-out visits, as well as supporting study

Qualifications

• 1 year independent monitoring experience, preferably in a CRO setting.
• Fluent in German (minimum C1 level)
• Ability to perform 5-7 visits per month nationwide

Responsibilities

• Conduct site initiation, monitoring, and close-out visits in accordance with study protocols, regulatory requirements, and SOPs.
• Perform site qualification, initiation, routine monitoring, and site closure activities with a focus on data integrity, patient safety, and protocol compliance.
• Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the study.
• Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and regulatory compliance.
• Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to meet timelines.
• Assist in the development and review of study-related documents, including protocols, informed consent forms, case report forms, and study manuals.
• Provide support and guidance to junior team members, including training, mentoring, and oversight as needed.

Skills

Independent monitoring

Fluent German

Visits per month

Job description

My client, a large International CRO are looking for experienced CRA's to join their team in Germany. This is working on behalf of an industry leading company, with projects available across a variety of therapeutic areas.

If you are an experienced CRA with a minimum of 1 years experience and are looking for a company where you can expediate your development, my client offers the perfect working environment to do just that due to the strong management team in place in Germany.

Please see expectations below:

• 1 years independent monitoring experience, preferably in a CRO setting
• Fluent in German (minimum C1 level)
• Ability to perform 5-7 visits per month nationwide

Responsibilities

• Conduct site initiation, monitoring, and close-out visits in accordance with study protocols, regulatory requirements, and standard operating procedures (SOPs).
• Perform site qualification, initiation, routine monitoring, and site closure activities with a focus on data integrity, patient safety, and protocol compliance.
• Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study.
• Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations.
• Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines.
• Assist in the development and review of study-related documents, including protocols, informed consent forms, case report forms, and study manuals.
• Provide support and guidance to junior team members, including training, mentoring, and oversight as needed.

If you meet the criteria above.