Kymera Therapeutics

Director, Data Management

Kymera Therapeutics • $195K — $275K *
Watertown, MA 02472In-Person
Pharmaceuticals & Biotech
11 - 15 years of experience
Today
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Job Overview by Ladders

Qualifications

  • 12+ years of experience in clinical data management in biotech or pharmaceutical industry
  • 7+ years managing vendor relationships in a global setting
  • Advanced knowledge of Data Management processes and systems
  • Strong understanding of CDISC standards
  • Experience with data visualization tools, preferably Elluminate
  • Familiarity with standardized medical terminology, such as MedDRA and WHODrug
  • Strong interpersonal, communication, and organizational skills.

Responsibilities

  • Act as Program Data Manager, overseeing all deliverables from DM CRO for multiple studies
  • Manage relationships with other functional areas to ensure quality data management
  • Oversee data collection tools and essential documents involved in the studies
  • Participate in and oversee User Acceptance Testing for Data Collection Tools
  • Perform quality control for data completeness and accuracy
  • Manage and mentor internal team members on the program
  • Support data cleaning, query generation, and review medical coding as needed
  • Ensure adherence to data management timelines and budget
  • Provide technical expertise for Data Management technologies
  • Contribute to development of procedures and best practices for internal processes

Benefits

  • Comprehensive benefits package
  • Opportunities for annual bonuses and equity participation
  • Performance-driven pay based on market standards
  • Recognition of results and capabilities through competitive compensation
Full Job Description


How you'll make an impact:
  • 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


Skills and experience you'll bring:
  • 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.


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 $195,000 - $275,000, 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 the capabilities they bring to the position.

About Kymera Therapeutics

Kymera Therapeutics is a clinical-stage biopharmaceutical company that is focused on discovering and developing novel small molecule therapeutics that selectively degrade disease-causing proteins by harnessing the body's own natural protein degradation system. The company's proprietary targeted protein degradation platform, Pegasus, is designed to harness the body's natural protein recycling machinery to degrade disease-causing proteins, with a focus on undruggable and difficult-to-drug targets. Kymera's initial programs are focused on oncology and immunology, with a goal of delivering transformative therapies for patients with previously untreatable diseases. Kymera was founded in 2015 and is headquartered in Cambridge, MA.
Learn more about Kymera Therapeutics
Size
75 employees
Market Cap
$1.4 billion
Industry
Pharmaceuticals & Biotech
Founded
2017
NASDAQ
KYMR
* Ladders Estimates

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