Remote Pharmaceutical Data Manager

Placements24; Kimberley; Hybrid; CAD 90,000 - 130,000; Full time

Benefits offered by this job

Fully remote

Professional development

Work-life balance

Job summary

Placements24 is seeking a highly skilled Remote Pharmaceutical Data Manager to oversee data collection, management, and integrity for clinical trials and studies. The role focuses on ensuring high-quality, regulatory-ready data for submissions, collaborating with clinical operations, biostatistics, and programming teams from a home-based setting.

The ideal candidate will have a Bachelor's in a scientific/CS field, 4+ years in clinical data management, strong EDC experience with Medidata Rave and

Qualifications

• Bachelor's degree in a scientific, statistical, or computer science field.
• Minimum of 4 years of experience in clinical data management within pharma or CRO.
• Proficiency with EDC systems (Medidata Rave, Oracle Clinical) and data management tools.
• Strong understanding of ICH-GCP guidelines and CDISC standards.
• Excellent analytical and problem-solving skills with meticulous attention to detail.

Responsibilities

• Develop and manage Clinical Data Management Plans (CDMPs) for clinical studies.
• Design, build, and validate study databases using EDC systems.
• Oversee data entry, data cleaning, and query resolution for accuracy.
• Develop and execute data validation checks and reporting procedures.
• Collaborate with biostatisticians and programmers to enable data analysis.

Skills

Clinical data management

Data quality

Remote collaboration

Education

Bachelor's degree in science/engineering/computer science

Tools

Medidata Rave

Oracle Clinical

Job description

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

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.