We are seeking a talented Clinical Programmer to join our innovative team. This position offers the opportunity to work remotely, contributing to cutting-edge clinical research projects while enjoying the flexibility of a remote work environment.
Responsibilities:
Develop and maintain clinical databases and data entry screens using industry-standard tools (e.g., SAS, Python, R).
Design and implement data validation checks to ensure data quality and integrity.
Generate and validate clinical trial data listings, summaries, and graphical displays.
Collaborate with cross-functional teams to support data management activities and ensure adherence to study protocols and regulatory requirements.
Provide technical expertise and support for electronic data capture (EDC) systems and related software.
Contribute to the development and implementation of programming standards and best practices.
Requirements:
Bachelor’s degree in Computer Science, Life Sciences, or related field.
Minimum of 3 years of experience in clinical programming within a CRO or pharmaceutical/biotech company.
Proficiency in programming languages and tools commonly used in clinical research (e.g., SAS, Python, R, SQL).
Strong understanding of CDISC standards and regulatory requirements (FDA, EMA).
Experience with electronic data capture (EDC) systems and clinical trial databases.
Excellent problem-solving and analytical skills.
Effective communication and collaboration abilities.
Benefits:
Competitive salary
Comprehensive benefits package
Remote work flexibility
Professional development opportunities
Collaborative and supportive team environment
Position Overview Clinical Data Specialist:
We are seeking a talented Clinical Programmer to join our innovative team. This position offers the opportunity to work remotely, contributing to cutting-edge clinical research projects while enjoying the flexibility of a remote work environment.
Responsibilities:
Perform data management activities for clinical trials, including data entry, validation, and cleaning.
Ensure data quality and integrity according to study protocols, regulatory requirements, and industry standards.
Develop and maintain data management documentation, including data validation plans and data management plans.
Collaborate with cross-functional teams to resolve data discrepancies and queries promptly.
Support database setup, testing, and maintenance activities.
Contribute to the development and implementation of data management processes and standards.
Requirements:
Bachelor’s degree in Life Sciences, Computer Science, or a related field.
Minimum of 3 years of experience in clinical data management within a CRO or pharmaceutical/biotech company.
Proficiency in clinical data management software (e.g., Medidata Rave, Oracle Inform, OpenClinica).
Strong understanding of GCP, CDISC standards, and regulatory requirements (FDA, EMA).
Excellent attention to detail and organizational skills.
Effective communication and collaboration abilities.
Benefits:
Competitive salary
Comprehensive benefits package
Remote work flexibility
Professional development opportunities
Collaborative and supportive team environment