Join our dynamic team as a Clinical Research Coordinator. You will oversee clinical trial processes, coordinate participant recruitment, and ensure adherence to protocols and regulations in a fast-paced environment.
Responsibilities
Oversee daily trial operations and monitor study progress.
Manage budgets and resource allocations for trials.
Evaluate and report on trial outcomes and participant safety.
Develop relationships with stakeholders including sponsors and regulatory bodies.
Prepare and present trial updates to senior management.
Attend meetings and provide input on research strategies.
Requirements
Education
Bachelor's degree in Life Sciences or related field
Master's degree is an advantage
Experience
3+ years of experience in clinical research
Technical Skills
Clinical Trial Management
Regulatory Compliance
Soft Skills
Attention to Detail
Communication
Certifications
Clinical Research Associate (CRA)
Good Clinical Practice (GCP)
Languages
English: Fluent
Advantageous
Experience with electronic data capture systems: Familiarity with EDC systems like Medidata or Veeva.
Knowledge of statistical analysis software: Understanding of tools like SPSS or SAS.
Benefits
Competitive salary and performance-related bonuses
Health and dental insurance
Flexible working hours
Professional development opportunities
Company Culture
Innovation: We encourage innovative thinking and continuous improvement in our research processes.
Collaboration: Teamwork is at the heart of what we do, promoting a supportive work environment.
Integrity: We uphold the highest ethical standards in all our research practices.