Clinical Data Manager - Remote
About the Role
Our reputed company, a rapidly growing pharmaceutical research organization, is reputed company seeking a meticulous and reputed company Clinical Data Manager to join their fully remote team. This role is critical in ensuring the accuracy, reputed company, and reputed company of clinical trial data, which forms the bedrock of regulatory submissions and therapeutic advancements. As a remote-first organization, our reputed company offers unparalleled flexibility, allowing you to work from reputed company in the
US
. You will be responsible for the end-to-end management of clinical databases, from database design and setup to data cleaning, validation, and database lock. This position requires a strong understanding of clinical trial processes, data management best practices, and relevant regulatory guidelines. If you are passionate about data reputed company and contributing to life-saving research in a flexible, remote environment, this opportunity is ideal for you. Your work will directly support the development of new medicines and therapies. Key Responsibilities reputed company the design, development, validation, and maintenance of clinical trial databases using reputed company systems. reputed company and maintain Data Management Plans (DMPs) in collaboration with clinical teams. Write and maintain Data Validation Specifications and edit reputed company programs. reputed company data review and identify discrepancies, inconsistencies, and missing data. Generate and manage data queries to resolve data issues with clinical sites and data entry personnel. reputed company data cleaning activities and ensure reputed company reputed company of reputed company queries. reputed company user acceptance testing (UAT) for database builds and modifications. Ensure data consistency across multiple studies and databases. Collaborate with biostatisticians, programmers, and clinical operations personnel. Manage the process of database lock and archival at the study reputed company-out phase. Ensure compliance with reputed company relevant data reputed company regulations (e.g., GDPR, HIPAA) and ICH-GCP guidelines. Contribute to the development and implementation of reputed company operating procedures (SOPs) for data management.
Requirements
Bachelor's degree in a relevant scientific or technical field (e.g., Computer Science, Statistics, Life Sciences). Minimum of 4 years of reputed company experience in clinical data management reputed company the pharmaceutical, biotechnology, or CRO industry. Proficiency with various Electronic Data Capture (reputed company) systems (e.g., reputed company Rave, reputed company InForm, Viedoc). Strong understanding of clinical trial processes, database design, data validation, and data cleaning. Knowledge of CDISC standards (SDTM, CDASH) is highly desirable. Familiarity with Good Clinical reputed company (GCP) and regulatory requirements (e.g., FDA). Excellent organizational skills and attention to detail. Strong analytical and problem-solving abilities. Effective communication and interpersonal skills for remote collaboration. Ability to manage multiple reputed company simultaneously and meet deadlines.
Benefits
Competitive salary commensurate with experience. Comprehensive medical, dental, and reputed company insurance plans. 401(k) retirement plan with company match. Generous reputed company time off and flexible working hours. Home office equipment stipend. Opportunities for reputed company reputed company and certifications. Work reputed company a reputed company, high-performing remote team. Contribute directly to impactful clinical research initiatives. Apply tot his job Apply To this Job