As a Clinical Research Associate, you will be integral in executing clinical trials. You will monitor and report on study efficacy, manage compliance with health regulations, and work closely with data management to ensure accuracy.
Responsibilities
Oversee the planning and implementation of clinical research studies.
Ensure compliance with ethical and regulatory standards at all times.
Assess and manage study-related data discrepancies.
Develop and maintain study documentation, including study protocols.
Conduct interim analyses to ensure the study is on track.
Coordinate with laboratory and data management teams for sample and data processing.
Facilitate communication among all stakeholders involved in the study.
Identify and resolve potential problems that may arise during studies.
Ensure all site personnel remain trained and informed throughout the study.
Stay current with relevant regulations and guidance impacting clinical research.
Requirements
Education
Bachelor's degree in a relevant field
Postgraduate qualification preferred
Experience
3-5 years of experience in clinical trials or medical research
Technical Skills
Regulatory Knowledge
Project Management
Soft Skills
Team Leadership
Conflict Resolution
Certifications
Clinical Research Coordinator (CRC)
Advanced GCP Certification
Languages
English: Fluent
Advantageous
Experience in Patient Recruitment Strategies: Knowledge of methodologies for effectively recruiting trial participants.
Familiarity with Budget Management: Ability to assist in managing project budgets and financial planning.
Benefits
Health coverage including dental and vision
Quarterly performance bonuses
Work-life balance initiatives
Support for further education and certifications
Company Culture
Passion for Discovery: We are passionate about advancing medical science and improving patient outcomes.
Continuous Improvement: Our teams are committed to professional growth and continuous learning.
Ethical Standards: Upholding the highest ethical standards in research is our core value.