We are seeking a dedicated Clinical Research Associate to join our growing team in Dundee. The ideal candidate will have experience in conducting clinical trials, with a strong focus on patient safety and data integrity.
Responsibilities
Manage relationships with clinical trial sites and investigators.
Conduct ongoing risk assessments throughout the trial.
Monitor patient safety and report any adverse events.
Assist in data management and data entry processes.
Ensure all trial-related activities comply with regulatory standards.
Prepare study materials for initiation and training sessions.
Coordinate patient recruitment strategies and outreach.
Assist in the development of study protocols and amendments.
Evaluate data collection methods for accuracy and reliability.
Document and report study findings and outcomes.
Requirements
Education
Bachelor's degree in Nursing or Clinical Research
Relevant certifications in Clinical Research are advantageous
Experience
3+ years of experience in a clinical research environment
Technical Skills
Regulatory Compliance
Patient Recruitment
Soft Skills
Problem-solving
Team Collaboration
Certifications
Clinical Research Coordinator (CRC)
GCP Certification
Languages
English: Fluent
Advantageous
Familiarity with statistical analysis software: Experience using software like SPSS or SAS for data analysis.
Knowledge of therapeutic areas: Insight into specific therapeutic areas such as oncology or cardiology.
Benefits
Generous annual leave and sick leave
Health insurance covering medical, dental, and vision
Opportunities for continuous training and certifications
Employee assistance program for wellbeing
Company Culture
Empowerment: We empower our employees to take ownership of their work, driving personal and professional growth.
Diversity and Inclusion: Our commitment to diversity and inclusion ensures a variety of perspectives, enhancing our research outcomes.
Community Engagement: We actively engage with the community to promote health and wellbeing beyond our clinical trials.