Senior Data Manager

6 days ago

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ResearchEd

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ResearchEd is an education policy research nonprofit providing objective analysis, deep insights, and detailed recommendations for education institutions and research organizations seeking to support equitable student outcomes and promote community and economic development through education. ResearchEd conducts student-centered work, particularly focusing on underserved groups, and provides research, data capacity building support, and advocacy. Their mission is to empower action in education, aiming for equitable access to education as a catalyst for community success and social justice.

education research • public policy • community college • rural education • Postsecondary Data Partnership

11 - 50 employees

Founded 2020

📚 Education

🤝 Non-profit

🌍 Social Impact

📋 Description

• As the Senior Data Manager (Sr. DM) you will be a key member of the Data Management Team. • Senior Data Managers serve as a key member of project teams, responsible for managing all data management tasks from project start-up to database lock, to producing a clean and analyzable database. • The Sr. DM will work closely with the Manager and/or Director, Data Management to support the data management capabilities and processes within Catalyst to provide efficient data management to clinical study teams.

🎯 Requirements

• Education: Bachelor’s degree in one of the life sciences, or equivalent knowledge and experience. • Experience: Seven plus years of clinical data management experience in pharmaceutical industry and/or contract research organization. • Extensive experience as a Lead Data Manager • Required Skills: Team player with ability to learn new things and teach others. • Ability to work well with technical and clinical team members and collaborate with entire clinical team (CRAs, Safety, Bios, etc.) and maintain positive and open relations with internal, sponsor, and vendor team members. • Ability to facilitate team meetings. • Knowledge of clinical trials concepts. • Ability to create detailed DM project instructions and documents (CRF guidelines, trial design document, edit check specifications, data review plan, etc.) • Proficiency with data processing systems (EDC systems, preferably RAVE). • Proficiency with Catalyst SOPs, WPs for general and DM operations. • Solid understanding of Good Clinical Practices and relevant regulatory guidelines. • Familiarity with CDISC standards. • Efficient with organizational skills to meet deadlines. • Organized and thorough with attention to detail. • Effective interpersonal skills and excellent communications skills, verbal, written and listening. • Ability to accept constructive criticism. • Effective logical thinking ability regarding problem-solving skills. • Proficiency in computer applications and time management tools (Excel, Word, Outlook, Project, etc.) • Potential ability to travel for meetings or training activities.