Senior Clinical Research Associate – CNS/Oncology

Jobtailor; Deutschland; Vor Ort; EUR 60.000 - 85.000; Vollzeit

Zusammenfassung

Jobtailor is seeking an experienced Clinical Research Associate based in Germany to manage clinical site activities for Worldwide’s projects. You will identify sites, support study start-up and contracting, and train site staff to ensure proper data collection and safety reporting.

Travel to sites is expected, with remote site management as needed. The role requires a strong CNS and Oncology background, English fluency, and a 4-year degree or RN/BSN nursing qualification, plus proficiency in

Qualifikationen

• Excellent interpersonal, oral, and written communication skills in English (required).
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Willingness to travel.
• Strong CNS and Oncology experience required.
• Hematology experience is a plus.

Aufgaben

• Manage research activities at sites participating in Worldwide’s clinical projects.
• Identify potential sites for research participation.
• Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations.
• Train sites to collect data properly and report potential safety-related events.
• Manage site activities during study maintenance.
• Close research activities at sites after study conclusion.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements.
• Perform most site management efforts remotely.

Kenntnisse

English proficiency

Interpersonal skills

Organizational skills

Independent work

Willingness to travel

CNS experience

Oncology experience

Hematology experience

Ausbildung

Four-year university degree

RN/BSN in Nursing

Tools

Microsoft Office

CTMS

EDC systems

Jobbeschreibung

• Manage research activities at sites participating in Worldwide’s clinical research projects
• Identify potential sites for research participation
• Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations
• Train sites to collect data properly and report potential safety-related events
• Manage site activities during study maintenance
• Close research activities at sites after study conclusion
• Conduct study initiation visits (SIVs)
• Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements
• Perform most site management efforts remotely

Requirements

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to detail
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS, and EDC systems
• 5+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Willingness to travel
• Strong CNS and Oncology experience required
• Hematology experience is a plus

Core Competencies

Demonstrates expertise in managing clinical research activities, ensuring compliance with regulatory requirements, and effectively training site personnel. Proficient in utilizing CTMS and EDC systems while maintaining strong organizational and communication skills.

Highest-signal resume keywords

• Clinical Research Associate Experience
• CNS Experience
• Oncology Experience
• Proficiency in Microsoft Office
• CTMS and EDC Systems

ATS Optimization Keywords

Hard Skills

• Clinical Research Management
• Regulatory Document Collection
• Data Collection Training
• Safety-Event Reporting
• Study Start-Up Activities
• Study Maintenance Management
• Study Initiation Visits
• Site Management
• Budget Negotiation
• Contract Negotiation

Soft Skills

• Interpersonal Skills
• Oral Communication Skills
• Written Communication Skills
• Organizational Skills
• Attention to Detail

Certifications & Qualifications

• 4-Year University Degree
• RN/BSN in Nursing

Industry Keywords

• Clinical Research
• Informed Consent
• Safety-Event Reporting
• Regulatory Compliance
• Hematology

Tools & Technologies

• Microsoft Office
• CTMS
• EDC Systems