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Clinical Research Associate Lead
3 weeks ago
- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
- Develop tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and standard operating procedures.
- Collaborate with cross-functional teams to ensure successful trial execution, including working with project managers, data managers, biostatisticians, and regulatory affairs specialists.
- Evaluate overall performance of site and site staff, provide recommendations regarding site-specific actions, and communicate serious issues to the project team.
- Bachelor's degree in a related field.
- Minimum of 5 years of experience in clinical research monitoring.
- In-depth knowledge of clinical trial processes and regulations.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
We are a leading global healthcare company dedicated to accelerating the delivery of innovative therapies. We believe that our success is directly linked to the success of our employees.
We offer a collaborative and dynamic work environment that fosters growth, development, and recognition.
Seniority Level:Mid-Senior level
Employment Type:Full-time
ClinicalResearch