Manager, Clinical Data Management

Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done. We want all of our people to go beyond what is possible. We aren't constrained by typical end rails, and we aren't out to just "treat" people. We're all in this for something more. We're driven to cure and motivated for change. Just imagine the possibilities of what we can do together. How You Will Achieve More: The Manager, Clinical Data Management is an integral part of the Clinical Data Management (CDM) team. They are a vital team member for operational excellence in partnership with Biostatistics, Development Operations, Statistical Programming, Medical and other Global Development functions. They provide day to day oversight and project management for CDM activities, including: EDC/ePRO development, implementation, and maintenance; data review and query management; vendor management; and the coordination and execution of data deliverables. Duties/Responsibilities Performs CDM activities for at least one clinical trial, ensuring all milestones are met for the study's life cycle (start-up, maintenance, and closeout). Oversees and manages EDC/ePRO implementation and maintenance for their trial(s), including oversight of UAT activities. Oversees the data review and query management activities Collaborates and supports the CDM Lead for the Program in executing the program's goals and maintaining consistency across studies. Is the CDM functional representative for the trial(s) at cross-functional and external (vendor/CROs) team meetings to ensure excellence in all aspects of clinical trial data acquisition, handling, and analysis. Performs oversight activities of CDM vendors on their trial(s). Ensures the trial operates in accordance with department standards and processes. Including ensuring the electronic Trial Master File (eTMF) is maintained and reviewed for the trial(s) on an ongoing basis. May contribute to the development of CDM processes, standards, templates. May collaborate on work streams and initiatives that impact the Biometrics and/or Clinical Development organizations. About You: Must have experience with the full CDM activity life cycle (start-up, maintenance, and closeout). Must have established knowledge and experience working with Medidata Rave EDC. Preferably also experience working with additional modules, such as Coder, Lab Administration, Safety Gateway, RCM, TSDV and/or eCOA. Knowledge of MedDRA and WHODrug coding and experience overseeing coding and SAE reconciliation activities for clinical trials. Ability to Translate Strategic Direction into short-term goals and objectives for your trial(s). Ability to Inspire Innovations & Problem Solving by seeking to improve how work gets done and inspiring other team members to do the same. Have a strong Personal Drive and the ability to Drive Performance of others. Ability to demonstrate Managerial Influence – motivating and holding people accountable up, down, and across the organization (as well as vendors). Be a strong Decision-Maker – ensuring appropriate stakeholders are involved, all relevant data are considered, conclusions are made, and actions items are appropriately followed. Excellent written and oral communication skills Deep understanding of drug development and biopharmaceutical industry preferred, including all industry standards and guidance (e.g., CDISC, Data Privacy regulations) Minimum BS/BA (or commensurate work experience) 6+ years relevant work experience with a focus on clinical data management Prolonged periods of sitting at a desk and working on a computer. #LI-Remote EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down. The base salary for this position is expected to range between $144,963.00 - $177,177.00 USD per year. The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors. Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company's discretion. For more information about Intellia's benefits, please click here. At Intellia, we are committed to solving the complex challenges of making CRISPR/Cas9-based medicines a reality for patients suffering from genetic diseases and to create novel engineered cell therapies for immuno-oncological and autoimmune diseases.