> Markdown version of [/jobs/ext/3322608-director-data-management](https://www.wearedevelopers.com/jobs/ext/3322608-director-data-management). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Director, Data Management - **Company:** KYMERA THERAPEUTICS - **Location:** Boston, MA, United States - **Experience:** Expert - **Salary:** $195,000.0 - $275,000.0 - **Contract:** Permanent contract - **Skills:** Clinical Data Management, Clinical Data Repository, Data Cleansing, Data Visualization, Data Analytics, Data Management - **Published:** September 9, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=464d82a01e2705ad ## About the Role * 12+ years' experience in clinical data management in biotechnology or pharmaceutical industry, with outsourced CRO oversight experience * 7+ years managing vendor relationships/partnerships in a global environment. * Must have advanced knowledge of Data Management processes and systems * Solid understanding of CDISC standards required * Data Visualization Tool (e.g Elluminate) experience preferred. * Experience using standardized medical terminology, including but limited too MedDRA and WHODrug. * Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a study team environment. ## Description * PIONEER: We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. * COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. * BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard., * Act as Program Data Manager, overseeing all deliverables of activities outsourced to DM CRO for multiple studies in a program. * Interact and manage relationships with other functional areas to ensure high quality data management activities * Oversight of data collection tools (EDC, DTAs, EDC integrations) and essential documents (DMP, UAT Documents, data edit specifications, annotated case books and data entry guidelines) * Participate and oversee User Acceptance Testing Activities for the applicable Data Collection Tools * Perform Quality Control for the data completeness and accuracy. * Manage and/or mentor internal team members supporting the program. * Participate in and support data cleaning, query generation and resolution and review of medical coding as needed. * Responsible for adhering to the Data Management timelines and budget. * Provide technical expertise to help in the use of technologies for Data Management and the clinical study team. * Contribute to the development of lessons learned and best practices as well as help develop SOPs and internal working procedures and process improvement initiatives. * Contribute to the establishment of systems and tools to help ensure clinical data security and integrity. * Contribute to the process to identify, evaluate and select external business partners and technology vendors