Clinical Research Associate - Neurology, Oncology - Germany

Worldwide Clinical Trials; Germany (OH); On-site; USD 75,000 - 105,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to work across therapeutic areas such as Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. You will handle regulatory submissions, TMF management, and site management support with experienced colleagues.

You will monitor sites, mentor junior CRAs, and ensure protocol adherence, safety reporting and data quality across studies. Travel to sites is required, and a 4-year degree or RN/BSN is expected.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Proficiency in Microsoft Office, CTMS and EDC Systems.
• 2+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Experience in Neurology, Oncology and Hematology is required.
• Willingness to travel.

Responsibilities

• Responsible for site qualification, initiation, interim monitoring, site management, and study close‑out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
• Provide applicable updates for site‑related documentation for filing in the TMF.
• Ensure site compliance with IP receipt, accountability and return or destruction.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

Skills

Interpersonal communication

Oral communication

Written communication

Microsoft Office

CTMS

EDC Systems

Education

4-year degree or RN/BSN

Tools

Microsoft Office

CTMS

EDC Systems

Job description

About Worldwide Clinical Trials

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are a global team of over 3,500+ experts, bright thinkers, dreamers and doers, and together we are changing the way the world experiences CROs – in the best possible way.

Role: Clinical Research Associate (CRA)

As a Clinical Research Associate at Worldwide, you will work alongside brilliant minds across diverse therapeutic areas, including Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is encouraged and ingrained in our culture. This role involves regulatory submissions, Trial Master File (TMF) management, and in‑house support for projects with heavy site management needs.

Responsibilities

• Responsible for site qualification, initiation, interim monitoring, site management, and study close‑out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
• Provide applicable updates for site‑related documentation for filing in the TMF.
• Ensure site compliance with IP receipt, accountability and return or destruction.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

Key Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to details.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS and EDC Systems.

Experience

• 2+ years of experience as a Clinical Research Associate.
• 4‑year university degree or RN/BSN in Nursing.
• Experience in Neurology, Oncology and Hematology is required.
• Willingness to travel required.

Equality & Diversity

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.