Data Manager Consultant (Remote)

About the Role

The Data Manager Consultant position at ClinChoice is a vital role within a global full-service Contract Research Organization (CRO) that emphasizes professional development and work-life balance. As a Data Manager, you will lead data management activities essential for the success of clinical trials, ensuring that data integrity and quality standards are upheld throughout the study lifecycle. Your first few months will involve collaborating with cross-functional teams, developing critical documents, and setting up databases to maintain project timelines. This position not only contributes to improving patient outcomes but also allows you to hone your skills in clinical research data management.

Key Responsibilities

• You will lead data management activities, ensuring that all deliverables meet established timelines and quality standards, which is crucial for the overall success of clinical trials.
• Your role will involve reviewing clinical research documents such as study protocols and Case Report Forms (CRFs) to ensure accuracy and compliance.
• Creating and reviewing electronic Case Report Form (eCRF) specifications will be part of your responsibilities, requiring attention to detail and a thorough understanding of data capture processes.
• Developing essential data management documents, including the Data Management Plan and Data Validation Plan, will be key to guiding the data handling process.
• You will also perform User Acceptance Testing (UAT) on data entry screens and edit checks to ensure that all systems function properly and meet user needs.
• Training clinical team members and site staff on data management processes will be a critical component of your work, ensuring that everyone is aligned on expectations and procedures.
• Ongoing data review and reconciliation activities will be part of your daily tasks, where you will monitor data clean-up efforts and provide metrics to track progress.

Requirements & Qualifications

• A Bachelor’s degree in clinical, pharmacy, biological, mathematical sciences, or a nursing degree is required to ensure a strong foundation in relevant fields.
• You should possess at least three years of data management experience or related work in the pharmaceutical industry, showcasing your proficiency in the field.
• Demonstrable knowledge of clinical research processes, regulatory requirements, and terminology is essential to navigate the complexities of clinical trials.
• Experience with several Electronic Data Capture (EDC) systems such as Medidata Rave, Oracle InForm, OpenClinica, and Medrio is highly preferred.
• Strong verbal and written communication skills will be necessary for effective collaboration and documentation within the team and with external stakeholders.

What You’ll Gain

• This role provides the opportunity to develop specialized skills in data management and analysis, crucial for a career in clinical research.
• You will gain hands-on experience with cutting-edge technology and methodologies in the pharmaceutical industry, enhancing your technical expertise.
• Working in a collaborative environment will help you build valuable relationships and networks within the clinical research community.
• Opportunities for professional growth and development are abundant, paving the way for advancement into senior data management or project management roles in the future.

How to Apply

If you are interested in this exciting opportunity, please submit your application. For additional details, you can Apply here.