Clinical Data Manager - Pharmaceutical Trials

Placements24; Bloemfontein; Hybrid; ZAR 600.000 - 1.000.000; Vollzeit

Zusammenfassung

Placements24 is seeking a meticulous Clinical Data Manager for a fully remote role. You will manage clinical trial data end-to-end, from database setup to lock, ensuring accuracy, completeness, and data integrity.

Responsibilities include CRF design, data management planning, cleaning, validation, and discrepancy resolution while collaborating with clinical operations, biostatisticians, and site personnel. The role emphasizes data quality and regulatory compliance in a flexible, remote work

Qualifikationen

• End-to-end management of clinical trial data from database setup to database lock.
• Design CRFs and data collection instruments to ensure data capture aligns with study protocols.
• Develop data management plans and data governance standards.
• Perform data cleaning, validation, and discrepancy management to ensure data integrity.

Aufgaben

• Oversee data management activities for multiple clinical studies.
• Collaborate with biostatisticians, clinical operations, and site personnel in a remote setting.
• Ensure regulatory and SOP compliance in data handling and reporting.
• Prepare data listings and interact with data managers during database lock and study reporting.

Kenntnisse

Clinical data management

Data quality assurance

Regulatory compliance

Study coordination

Ausbildung

Bachelor's degree in Life Sciences or related field

Tools

EDC (e.g., Medidata Rave)

CDMS/CTMS software

Jobbeschreibung

About the Role

This is a fully remote position for a meticulous Clinical Data Manager to support our client's diverse pharmaceutical research initiatives. You will be responsible for the end-to-end management of clinical trial data, ensuring its accuracy, completeness, and integrity from database setup to database lock. Your duties will include designing Case Report Forms (CRFs), developing data management plans, performing data cleaning and validation activities, and managing data discrepancies. This role is crucial for generating reliable data that forms the basis of clinical study reports and regulatory submissions. Working remotely, you will collaborate with clinical operations teams, biostatisticians, and study site personnel. We provide a flexible work environment and the tools necessary to succeed in a data-driven field. If you are passionate about data quality and contributing to medical advancements, this remote opportunity is ideal for you. Your attention to detail and commitment to data excellence will be highly valued in this key role supporting critical pharmaceutical research.