We are seeking a Clinical Research Coordinator to manage clinical trials and ensure compliance with regulations. You will play a vital role in patient recruitment and data management to enhance our research efforts.
Responsibilities
Oversee all aspects of clinical trials and ensure adherence to protocols.
Collaborate with interdisciplinary teams for trial success.
Track participant progress and report findings.
Ensure the quality of research data collected.
Manage budgets and resources allocated to research projects.
Facilitate training sessions for study staff.
Prepare and submit progress reports to stakeholders.
Monitor compliance with ethical standards.
Investigate and resolve study-related issues as they arise.
Contribute to the continuous improvement of clinical processes.
Requirements
Education
Bachelor's degree in Pharmacy or related field
Master's degree in Clinical Research is preferred
Experience
5+ years of experience in clinical research
Technical Skills
Protocol Development
Statistical Analysis
Soft Skills
Problem-solving
Leadership
Certifications
Certified Clinical Research Associate (CCRA)
Advanced GCP Certification
Languages
English: Fluent
Advantageous
Previous experience in patient-focused trials: Hands-on experience working directly with trial participants.
Proficient in statistical software: Experience with software such as SPSS or SAS for data analysis.
Benefits
Comprehensive health and dental coverage
Generous pension contributions
Opportunities for professional development
Flexible work arrangements including remote options
Company Culture
Continuous Education: We support ongoing learning and development to keep our team at the forefront of clinical research.
Patient-Centered Focus: Our work revolves around enhancing patient care and outcomes through our research initiatives.
Integrity and Ethics: We uphold the highest ethical standards in all our research endeavors, ensuring transparency and trust.