Homeoffice Sr. Clinical Data Manager, Contractor chez Syndax Pharmaceuticals

Syndax Pharmaceuticals is looking for a Sr. Clinical Data Manager, Contractor

At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.

The Role: 

The position is responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This position applies broad expertise across specialized fields within clinical data management and related disciplines. This individual plays a key leadership role in the design, oversight, and execution of clinical data strategies that support high-quality, regulatory-compliant data deliverables. 

Key Responsibilities: 

• Lead all Clinical Data Management tasks for a project including the development of eCRFs, eCRF completion guidelines, Data Management Plan (DMP) and other Clinical Data Management documents in collaboration with applicable service providers and/or internal teams. 
• Oversee the implementation of project specific Clinical Data Management Systems and/or processes for assigned projects.
• Oversee the implementation of plans for the processing of data within established timelines and budget specifications, and make necessary adjustments based upon project needs. 
• Lead clinical data management activities from study start-up through database lock in collaboration with applicable service providers and/or internal teams. 
• Design, review, and finalize case report forms (CRFs) in collaboration with cross functional team members. 
• Develop and maintain data management plans, data review guidelines, and edit check specifications. 
• Oversee database development, validation, user acceptance testing and go live activities.
• Monitor data flow, ensure timely and quality data availability for analysis.
• Ensure compliance with standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements. 
• Review and contribute to clinical protocols and statistical analysis plans to ensure alignment with data collection objectives. 
• Manage and collaborate with external vendors, CROs, and partners related to outsourced data management tasks to ensure timely and quality data deliverables. 
• Represent data management in cross-functional meetings and communicate project status, risks, and resolutions. 
• Provide analysis and feedback (questions, issues and possible resolutions) to the line manager and/or project team on Clinical Data Management tasks, systems or processes. 
• Contribute to the development and improvement of data management processes and tools. 
• Monitor and manage study budgets to ensure financial efficiency and compliance. Assess change orders, evaluating cost overruns to mitigate financial risk while maintaining study integrity.  
• Train and mentor junior team members, promoting best practices in clinical data standards and compliance. 
• Participate in audits and inspections, contributing to the development of corrective and preventive actions. 
• Communicate with all departments as necessary regarding project status/issues. 
• Perform other duties as assigned.

Desired Experience/Education and Personal Attributes:

• Bachelor's degree in related scientific discipline.
• Minimum of 12 years related industry experience. 
• Strong understanding of CDISC standards (CDASH, SDTM), ICH-GCP, FDA, and other regulatory guidelines. 
• Expert knowledge of Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Veeva).  
• Experience with database design, development and user acceptance testing required. 
• Expert knowledge of clinical trial processes, data flow, and data cleaning best practices. 
• Excellent problem-solving skills with the ability to resolve complex technical issues. 
• Effective communication and leadership skills with the ability to influence cross-functional teams, levels, including executive leadership.  
• Experience working with CROs, vendors, and global clinical teams. 
• Proven track record leading data management for global clinical trials in a sponsor or CRO setting.  
• Demonstrates excellent written and verbal communication. 
• Strong organizational and prioritization abilities. 
• Exceptional critical thinking and project management skills. 
• Ability to handle multiple projects and work in a team environment. 

Location: While our corporate headquarters are located in New York City, this position is open to candidates from any location with a preference for east coast locations.  

About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.

Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

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