Remote Pharmaceutical Data Manager

Darum lohnt es sich

You will work closely with clinical operations, biostatistics, and programming teams to establish data management plans, design databases, and ensure adherence to global standards.

Benefits • Competitive salary and comprehensive benefits package. • Fully remote position offering significant work-life balance. • Opportunities for professional growth and advancement in clinical data management. • Access to cutting-edge data management technologies and training. • A supportive and collaborative team environment focused on scientific rigor and data integrity.

About the Role Our client is seeking a highly skilled and detail-oriented Remote Pharmaceutical Data Manager to oversee the collection, management, and integrity of data from clinical trials and research studies.

This fully remote position is critical for ensuring that high-quality, accurate, and reliable data is available to support regulatory submissions and decision-making processes.

This role offers a unique opportunity to contribute to life-saving research while enjoying the flexibility of working from home, utilizing advanced data management systems and adhering to rigorous quality standards.

Key Responsibilities • Develop and manage Clinical Data Management Plans (CDMPs) for clinical studies. • Design, build, and validate study databases using Electronic Data Capture (EDC) systems. • Oversee data entry, data cleaning, and query resolution processes to ensure data accuracy and completeness. • Develop and execute data validation checks and reporting procedures. • Ensure compliance with ICH guidelines, GCP , and relevant data privacy regulations. • Collaborate with biostatisticians and programmers to facilitate data analysis and reporting.

Requirements • Bachelor's degree in a scientific, statistical, or computer science field. • Minimum of 4 years of experience in clinical data management within the pharmaceutical or CRO industry. • Proficiency with EDC systems (e.g., Medidata Rave, Oracle Clinical) and data management tools. • Strong understanding of clinical trial processes, ICH-GCP guidelines, and CDISC standards. • Excellent analytical and problem-solving skills, with meticulous attention to detail. • Effective communication and collaboration skills for a remote work environment.