Experienced Clinical Research Associate

Medpace; Frankfurt; Hybrid; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

An established industry player seeks a Clinical Research Associate to join their dynamic team. This role offers the chance to work on innovative projects that impact patient lives across Europe. With a focus on clinical development, you'll engage directly with medical staff, ensuring compliance and excellence in research practices. Enjoy a hybrid work model that promotes work-life balance and provides opportunities for professional growth. If you're passionate about making a difference in the medical field, this is your chance to shine in a supportive and forward-thinking environment.

Leistungen

Flexible working conditions

Competitive employee benefits

Annual merit increases

Variable compensation bonus plan

Casual dress code

Company-sponsored employee appreciation events

Competitive PTO packages

Qualifikationen

• Minimum university degree in health or life sciences required.
• 1.5 years experience as CRA or 2.5 years as CRC necessary.

Aufgaben

• Conduct qualification and monitoring visits for research sites.
• Verify investigator qualifications and ensure compliance with protocols.
• Complete monitoring reports and follow-up letters.

Kenntnisse

Clinical Research Associate (CRA)

Communication Skills

Time Management

Microsoft Office

German Language

English Language

Ausbildung

University Degree in Health or Life Sciences

Tools

Clinical Trial Management Systems

Jobbeschreibung

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.

What can Medpace offer you?

• Interesting projects, career advancement, and recognition and exposure to our international footprint.
• Flexible working conditions – Opportunity to work from home and flexible working hours
• Competitive employee benefits
• Annual Merit increases
• Variable Compensation Bonus Plan
• Fast PACE – Accelerated, tailored training program training program based on your experience
• Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager
• Casual Dress Code

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 as a CRA or 2.5 years as CRC.
• 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.

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.

• Hybrid and work-from-home options (dependent upon position and level)
• Competitive PTO packages
• Company-sponsored employee appreciation events
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth

Awards

• Recognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022 and 2023
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.