Associate Director, Data Management New Waltham, MA

Zenas BioPharma is a global biopharmaceutical company committed to becoming a leader in the development and commercialization of immune-based therapies for patients around the world. With clinical development and operations globally, Zenas is advancing a deep and balanced global portfolio of potential first- and best-in-class autoimmune therapeutics in areas of high unmet medical need while meeting the value requirements of the dynamic global healthcare environment. The company’s pipeline continues to grow through our successful business development strategy. Our experienced leadership team and network of business partners drive operational excellence to deliver potentially transformative therapies to improve the lives of those living with autoimmune and rare diseases.

We are seeking top talent who share our commitment to patients and have a track record of success in acquiring, developing and commercializing products across the globe. Our colleagues have an opportunity to engage in a fast-paced learning environment and experience individual and organizational success as we work towards becoming a global immunology and autoimmune disease leader, while living our values of Transparency, Relationships, Urgency, Excellence and Innovation – TRUE Innovation !

Position Summary

The Associate Director, Clinical Data Management will drive the entire life cycle of key Zenas Data suppliers, from identification, selection, and on-boarding to performance management. This is an important cross-functional leadership position supporting within the R&D organization. This individual will work with Zenas leaders on strategy development, cost management, and performance management of key data vendors to ensure that desired goods or services, quality, and performance meet business needs. This role requires the ability to develop and maintain strong collaborative and cooperative working relationships with team members across different functions and at different levels within the organization, in a manner consistent with our principle of TRUE Innovation. This position reports to the Executive Director, Data Management.

Key Responsibilities

• Implement data management vision for clinical data management on studies assigned by overseeing all clinical data management activities
• Manage the CRO / vendor for clinical data management activities on studies assigned including leading, overseeing, and approving CRO data management documentation (e.g., Case Report Form (CRF) specifications, CRF Completion Guidelines, Data Validation Specifications, Data Transfer Specifications, Data Management Plans, external reconciliations) to assure processes meet the protocol requirements ensuring data integrity and regulatory compliance
• Develop strong relationships to optimize collaborative cross-functional engagement internally and with vendors to align with company priorities, goals, and objectives
• Build and maintaining CRF standards to achieve cost efficiencies with external vendors and time efficiencies with Zenas colleagues
• Lead the cross-functional team in user acceptance testing of the clinical database to align with protocol and analysis needs for the collection and cleaning of data
• Assist the Head of Data Management by providing data management expertise in the preparation of project specific request for proposals, reviewing vendor specifications / budgets, and discussing / recommending vendor selection
• Write protocol specific oversight data review plans on studies assigned, facilitate the cross-functional oversight data review preparation and meetings including following all data issues to resolution
• Effectively manage functional area on assigned studies (resources, activities, processes, and documentation)
• Proactively identify potential data issues / risks plus recommend and implement solutions on assigned studies.
• Collaborating with internal colleagues providing clinical data management expertise, leadership, and support to other functional leads to meet and maintain cross-functional excellence to meet company objectives.
• Manage aspects of clinical data management activities, including vendor performance, internal metrics, quality assurance checks, and communication of study status within and outside the study team on assigned studies..
• Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents by regularly auditing the Data Management section of the TMF to ensure complete and current CRO filing to meet regulatory requirements on assigned studies.

Qualifications

Base salary pay range for this role is $152,000 to $191,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and / or location.

Zenas believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Zenas’ competitive total rewards strategy that also includes annual performance bonus, equity, full range of benefits and other incentive compensation plans.

Zenas BioPharma is proud to be an equal opportunity employer. We are committed to fostering an environment where diversity is valued. All qualified applicants will receive consideration for employment based on merit, qualifications and the needs of the business.

All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, creed, sex, sexual orientation, pregnancy or pregnancy-related conditions, gender identity, genetic information, marital status, familial status, national origin, ancestry, ethnicity, protected veteran status, age, disability or any other factors prohibited by law.

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