Join a dynamic team as a Principal Clinical Database Programmer. Work remotely while leading innovative database solutions for clinical trials. Enhance your expertise in biostatistics and data management.
Biostatistics
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical database programming efforts for a remote position with a focus on biostatistics and data management.
- Collaborate with cross-functional teams to ensure accurate data collection and reporting for clinical studies.
- Utilize advanced programming techniques to optimize database functionality and performance.
- Develop and maintain database standards to ensure compliance with regulatory requirements.
- Provide technical leadership and mentorship to junior database programmers.
- Contribute to the design and implementation of innovative data solutions for clinical trials.
- Work remotely, offering flexibility and autonomy in a dynamic environment.
- Engage in continuous learning to stay updated with industry trends and technologies.
Key Responsibilities & Duties
- Design and implement clinical databases to support biostatistical analysis and reporting.
- Ensure data integrity and accuracy through rigorous validation and quality control processes.
- Collaborate with biostatisticians to define data requirements and analysis specifications.
- Develop and execute database programming scripts to automate data workflows.
- Provide technical support and troubleshooting for database-related issues.
- Document database designs, programming scripts, and validation procedures.
- Participate in project planning and timeline estimation for database programming tasks.
- Train and mentor team members on database programming best practices.
Job Requirements
- Bachelor of Science (BS) degree in a relevant field is required.
- Minimum of 8 years of experience in clinical database programming; 9 years preferred.
- Proficiency in database programming languages and tools used in clinical research.
- Strong understanding of biostatistics and clinical data management principles.
- Experience with regulatory compliance standards for clinical trials.
- Excellent problem-solving skills and attention to detail.
- Ability to work independently in a remote setting while collaborating effectively with teams.
- Leadership skills to mentor and guide junior programmers.
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