Experienced Clinical Research Associate - Sign-On Bonus eligible (multi-sponsor, multi-therapeu[...]

Medpace; Frankfurt (Oder); Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

A leading clinical research organization in Germany seeks an Experienced Clinical Research Associate to join their Clinical Operations team. The role involves conducting site visits, ensuring compliance with protocols, and maintaining communication with site staff. Ideal candidates will have at least 1.5 years of experience, a university degree in health or life sciences, and proficiency in German and English. This position offers a chance to grow within a dynamic and expanding organization and is associated with travel across Germany, Austria, and Switzerland.

Leistungen

Sign-On Bonus of up to 7,500 EUR

Qualifikationen

• Minimum of 1.5 years of previous experience.
• Must be detail-oriented and efficient in time management.
• Proven track record in clinical patient management.

Aufgaben

• Conduct qualification, initiation, monitoring, and closeout visits for research sites.
• Communicate with medical site staff including coordinators and physicians.
• Verify investigator qualifications, training, and resources.
• Perform regulatory document reviews.
• Complete monitoring reports and follow-up letters.

Kenntnisse

Detail-oriented

Time management

Proficient in Microsoft Office

Outstanding communication skills

Presentation skills

Experience in clinical patient management

Full proficiency in German and English

Ausbildung

University degree in health or life science

Jobbeschreibung

Job Summary

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical Operations team in Germany. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Qualified candidates are eligible for up to a 7.500 EUR Sign-On Bonus.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and / or investigational product / drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

• Must have a minimum of a university degree in a health or life science related field;
• Min.1.5 years of previous experience.
• Approximately 60-80% travel in Germany, Austria and Switzerland;
• Proficient knowledge of Microsoft® Office and general computer literacy;
• Outstanding communication and Presentation skills;
• Must be detail-oriented and efficient in time management;
• Excellent verbal and written communication skills; full proficiency in both German and English;
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities.