Experienced Clinical Research Associate (remote-based)

Medpace; Österreich; Vor Ort; EUR 45.000 - 60.000; Vollzeit

Benefits dieser Stelle

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths for growth

Employee appreciation events

Health and wellness initiatives

Zusammenfassung

A leading clinical research organization is seeking an Experienced Clinical Research Associate to join its Clinical Operations team in Austria. The position is home-based and involves driving the success of clinical activities. Candidates must have a university degree in a health or life science field, at least 1.5 years of CRA experience, and proficiency in English and German. The role includes site visits, communication with medical staff, and adherence to regulatory requirements, with travel across Germany, Austria, and Switzerland.

Qualifikationen

• Minimum 1.5 years of previous experience as a CRA.
• Ability to travel approximately 60-80% in Germany, Austria, and Switzerland.
• Demonstrated experience in clinical patient management and protocol.

Aufgaben

• Conduct qualification, initiation, monitoring, and closeout visits for research sites.
• Communicate with medical site staff and ensure compliance with protocols.
• Verify investigator qualifications and maintain good documentation practices.

Kenntnisse

Communication and presentation skills

Detail-oriented

Time management

Verbal and written communication in English and German

Ausbildung

University degree in health or life sciences

Tools

Microsoft Office

Jobbeschreibung

Overview

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical Operations team in Austria (home-based). 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!

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.

This role is home-based.

Qualifications

• Must have a minimum of a university degree in a health or life science related field;
• Min. 1.5 years of previous experience as a CRA;
• 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 in English and German;
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.