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Title
Text copied to clipboard!Clinical Research Specialist
Description
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We are looking for a dedicated Clinical Research Specialist to support our team in the planning, execution, and monitoring of clinical trials. In this role, you will be responsible for ensuring regulatory compliance, coordinating with study sites, and maintaining data quality. You will work closely with medical professionals, study coordinators, and external partners to ensure the integrity and efficiency of clinical research projects.
Your main tasks will include developing study protocols, submitting to ethics committees, and monitoring study progress. You will analyze study data, prepare reports, and contribute to the continuous improvement of study processes. Additionally, you will serve as a point of contact for questions regarding study methodology and regulatory requirements.
A solid understanding of GCP (Good Clinical Practice), ICH guidelines, and national and international regulations is essential. You should be able to interpret complex medical information and translate it into clear documentation. Experience with electronic data capture (EDC) systems and clinical databases is a plus.
This position requires a high level of organization, accuracy, and communication skills. You should be able to manage multiple projects simultaneously and work under tight deadlines. A scientific background in medicine, pharmacy, life sciences, or a related field is required.
If you are passionate about medical research and want to contribute to the development of new therapies, we look forward to your application.
Responsibilities
Text copied to clipboard!- Plan and conduct clinical trials
- Develop and review study protocols
- Communicate with study sites and ethics committees
- Ensure regulatory compliance
- Collect and analyze data
- Prepare study reports
- Ensure data quality
- Train study personnel
- Coordinate with interdisciplinary teams
- Support audits and inspections
Requirements
Text copied to clipboard!- Degree in medicine, pharmacy, life sciences, or related field
- Experience in clinical research
- Knowledge of GCP and ICH guidelines
- Familiarity with regulatory requirements
- Experience with EDC systems
- Excellent German and English skills
- Analytical thinking
- Organizational skills
- Teamwork
- Strong communication skills
Potential interview questions
Text copied to clipboard!- What experience do you have with clinical trials?
- How do you ensure GCP compliance?
- Which EDC systems have you used?
- How do you manage multiple projects simultaneously?
- How do you communicate with study sites?
- How do you stay informed about regulatory changes?
- How do you handle data discrepancies?
- What role does teamwork play for you?
- How do you prioritize tasks under pressure?
- What experience do you have with ethics committees?
