Drive success in clinical trials with Everest Clinical Research as a Clinical Safety Data Associate. Work in a flexible setting from home in Canada or at our Markham office, focusing on critical safety data review tasks.
As a Clinical Safety Data Associate, you will play a pivotal role ensuring the integrity and quality of safety data across various trials. This position demands a background in medical information management and the ability to collaborate effectively with multiple stakeholders. Candidates should possess a strong understanding of data coding and clinical trial processes.
Key Responsibilities:
- Coordinate development of safety data review protocols
- Conduct thorough reviews of clinical safety data
- Assist Clinical Data Managers in data handling
- Provide coding support using established dictionaries
- Engage with teams to resolve data discrepancies
Requirements:
- Relevant degree (RN, M.D., Pharm.D., etc.)
- 2-3 years' clinical data management experience
- Knowledge of safety data coding and analysis
- Effective communication at all levels
- Well-organized with strong multitasking skills
Bring your expertise in clinical safety data to Everest and enhance quality in groundbreaking research.
Clinical Research Safety Data Associate in Markham employer: Everest Clinical Research Services Inc
Everest Clinical Research is an exceptional employer located in the vibrant Greater Toronto Area, offering a dynamic work culture that prioritizes quality, customer focus, and flexibility. Employees benefit from a comprehensive package that includes medical, dental, and vision coverage, generous paid time off, and opportunities for professional growth through mentorship and training. Joining Everest means being part of a rapidly growing organization that values innovation and collaboration, making it an ideal place for those seeking meaningful and rewarding careers in clinical research.
Contact Details:
Everest Clinical Research Services Inc Recruitment Team
