Key Responsibilities:
- Work independently to manipulate and review subject data from multiple sources.
- Lead interdepartmental discussions to explore best strategies and practices.
- Provide concise updates to study teams and other key stakeholders.
- Assist with process development, improvement, and data assessments.
- Generate a thorough understanding of protocol schedules, contracts, budgets, and payment terms.
- Escalate performance issues and manage escalations regarding tracking system setup/maintenance issues.
- Contribute to general department documents and policies by assisting mentors with implementing best practices.
Qualifications and Skills:
- Bachelor’s degree in life science-related fields, Engineering, Biostatistics, or related fields.
- If possible, prior clinical research experience or related fields of 6 months to 1 year.
- Experience in data assessments, analytics, or critical assessments is preferred but not required.
- Understanding of database structure and complex data systems.
- Proficient in Microsoft Excel and quality control support.
- Excellent written and verbal communication skills, including proficiency in English.
- Strong attention to detail, problem-solving skills, and the ability to adapt to changing priorities.
- Demonstrated initiative, self-motivation, and a positive attitude.
Work Schedule: Standard (Mon-Fri)