Director, Clinical Data Management

Korro Bio • Cambridge, MA

5d

About The Position

Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform. Korro is generating a portfolio of differentiated programs that are designed to harness the body’s natural RNA editing process to effect a precise yet transient single base edit. By editing RNA instead of DNA, Korro is expanding the reach of genetic medicines by delivering additional precision and tunability, which has the potential for increased specificity and improved long-term tolerability. Using an oligonucleotide-based approach, Korro expects to bring its medicines to patients by leveraging its proprietary platform with precedented delivery modalities, manufacturing know-how, and established regulatory pathways of approved oligonucleotide drugs. Korro is based in Cambridge, Massachusetts. We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. Our values - Rewrite the future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Korro is a magnet for outstanding talent and a great place to work. Join us as we redefine what's possible in genetic medicine and work to make a lasting impact on human health. Reporting to the Vice President, Clinical Development Operations, the Director, Clinical Data Management supports the Clinical Development organization by providing expertise in all aspects of clinical data management for assigned study(ies). The person in this role will participate with both strategic and hands-on support, oversight of vendors/CROs, and contributions to departmental process and standards development Excellent written and oral communication skills are required, as is the desire and ability to work in a small, fast-paced, and patient-focused environment.

Requirements

• Bachelor's degree in Life Sciences, Computer Science, or a related field; advanced degree preferred.
• Minimum of 8 years of experience clinical data management/clinical trials is required.
• Experience with complex study designs and matrix management of vendors processing clinical data within/across studies and programs.
• Proficiency with technology associated with current and evolving data management practices, including electronic data capture, data aggregating, data visualization and analytics, automated data bots, machine learning/artificial intelligence-based process enhancements, etc.
• Proficient in clinical data collection/reporting/review and analysis processes using EDC platforms (i.e., Medidata, Veeva, ePRO, etc.) for Phase I-IV clinical trials in pharmaceutical industry/clinical research company.
• Knowledge of and experience with medical terminology, medical coding dictionaries (MedDRA, WHODrug), and quality control processes.
• Knowledge of industry and regulatory standards (FDA and EMEA Regulations, ICH Guidelines, and GCP) including CDISC standards (CDASH/SDTM).
• Ability to contribute to improving the quality of internal data management policies, programs and initiatives.
• Ability to work independently to manage multiple projects in a fast-paced environment.
• Excellent interpersonal skills and communication skills (verbal and written) with the ability to work independently and collaboratively in a dynamic team environment.
• Ability to thrive working in a fast-paced environment and manage a variety of projects simultaneously and handle rapidly changing information, where fearless innovation is a core value.
• Ability to clearly communicate, resolve complex issues, and mitigate risks.

Responsibilities

• Manage all data management (DM) tasks for clinical programs from study startup through database closure and archival, producing high-quality databases for analysis and potential regulatory submissions.
• The person in this role must have experience in a regulated environment and be prepared to present data and documentation in support of regulatory requirements for complete and accurate data.
• Manage the Data Management function at Korro and author, review, publish, and review policies and methods in standard operating procedures, work instructions, job aids, and other training documents.
• Work closely with cross-functional members of the study team, including Clinical Development, Biostatisticians, Statistical Programmers, Pharmacovigilance, Regulatory, Translational Research and Clinical Operations.
• Provide representation, and guidance to the internal and external teams as the clinical data management subject matter expert for assigned program/studies.
• Serve as a subject matter expert for various operations, including, but not limited to, electronic data capture, external data standardization, collection, and processing, and the creation of standard data collection forms and associated validation checks and collection processes.
• Oversee CRO data cleaning activities including processing queries, performing ongoing data review, identifying and tracking data issues and trends to give transparency to Global Development Program Leads, and other program team members.
• Provide input into study protocols, SAPs, and other clinical documents, to ensure quality data collection and management.
• Map data flows, processes and systems used for collection, management and provision of data to downstream functional area users.
• Contribute to data management deliverables including Data Management Plans, Data Validation Manuals, CRF Completion Guidelines, Data Transfer Specifications, Lab Specifications, etc.
• Support vendor UATs for database builds and or migrations to manage any impacts from mid-study updates to the EDC database.
• Meet with global regulatory agencies and mock auditors in quality, performance, and system audits and inspections and ensure inspections meet department performance metrics through pro-active compliance and quality measures.
• Develop data management standard working practices along with preparations and requirements for regulatory submissions and inspections.
• Establish data transfer guidelines for external data with CRO and vendor partners; reconcile and ensure transfers are executed to plan.
• Reconcile electronic data transfers from external vendors (e.g., IXRS, specialty labs, etc.) to the sponsor and/or oversee study data reconciliations performed by the CRO.
• Assume ownership for DM project deliverables within DM scope of services including overseeing overall quality, adherence to Study Plans and standard operating procedures.
• Coordinate with CRO on presentation of data metrics, trending and reports for data review meetings with internal stakeholders to ensure ongoing data integrity and proactive quality measures are employed to identify data issues.
• Assist in defining data listings, summary table validation, data specifications and/or process data transfers in preparation for statistical review and/or data management audits.
• Support close-out audit, as specified, for closing of study trial in EDC or other clinical data management DBs.
• Contribute to data system compliance by following the established guidelines of national and international regulatory authorities.

Benefits

• Korro offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance, a dependent care flexible spending account and a Company-funded health savings account and free parking.

What This Job Offers

• Job Type: Full-time
• Career Level: Director