Associate Director, Clinical Data Management

Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn . How we work: 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. How you’ll make an impact: Act as Lead Data Manager, overseeing all deliverables of activities outsourced to DM CRO for multiple studies 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 in User Acceptance Testing Activities for the applicable Data Collection Tools Perform Quality Control for the data completeness and accuracy. 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. Skills and experience you’ll bring: 8+ years’ experience in clinical data management in biotechnology or pharmaceutical industry, with outsourced CRO oversight experience 5+ 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 experience preferred. Experience using standardized medical terminology, including but not limited to MedDRA and WHODrug. Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a study team environment. Equal Employment Opportunity Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class. Compensation Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay. The anticipated base salary range for this role is $145,000 – $215,000, with eligibility for annual bonus, equity participation, and comprehensive benefits. Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and