Associate Director

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 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 contribute:

• 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.
• Contribute to the process to identify, evaluate and select external business partners and technology vendors

Skills and experience you’ll bring:

• 10+ 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 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.

This position is based in Watertown, MA, and offers a hybrid work model with a minimum of 3 days/week in the office.

Skills and experience not an exact match?:

Go ahead and submit your resume (and a cover letter, if you’d like!).  If this role isn’t right for you, we can keep you in mind for future opportunities.

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.