Clinical Research Associate
vor 4 Wochen
Medpace is a leading contract research organization (CRO) offering a unique opportunity to contribute to the development of innovative medical treatments. As a Clinical Research Associate, you will play a vital role in ensuring the success of clinical trials, working closely with cross-functional teams to deliver high-quality results.
Key Responsibilities:- Conduct site initiation, monitoring, and closeout visits to ensure compliance with protocols and regulations.
- Communicate effectively with site staff, investigators, and other stakeholders to ensure seamless trial execution.
- Verify investigator qualifications, training, and resources to ensure trial feasibility.
- Review and verify medical records, research source documentation, and case report form data to ensure accuracy and compliance.
- Assess site performance, identify areas for improvement, and provide recommendations to enhance trial success.
- University degree in a health or life science-related field.
- Approximately 60-80% travel required.
- Proficient in Microsoft Office and general computer literacy.
- Excellent communication, presentation, and time management skills.
- Fluency in German and English.
At Medpace, we are committed to accelerating the development of safe and effective medical treatments. Our team of experts is dedicated to delivering high-quality results, and we offer a dynamic work environment with opportunities for growth and development. Join us in our mission to make a difference in the lives of patients and families worldwide.
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