• The Director, Corporate Governance provides strategic leadership and oversight of the company’s corporate governance operations • Responsible for maturing the governance framework, advising on governance issues, preparing board materials, subsidiary management, and ensuring alignment with regulatory requirements, industry best practices, and organizational strategy • Partners closely with senior executives, the Corporate Secretary, and board members • Serves as a trusted advisor to senior leadership and the board on governance matters and leads initiatives that strengthen governance processes, mitigate risk, and enhance organizational integrity • Leads and develops a team of corporate governance professionals, driving operational excellence, continuous improvement, and strong cross-functional collaboration across the enterprise

Role Description Experienced safety surveillance and risk management scientist with a degree in life sciences (Pharmacy degree, Nursing degree or master’s degree in health-related field) and 10+ years’ experience in safety surveillance and safety risk management. Have an in depth understanding on FDA and EU-GVP guidance on safety signal management, periodic report development, safety risk management and benefit-risk assessment. Detail-oriented and have strong written, organizational and communication skills. Will work collectively with all relevant functions for DSPV including R&D medicine, clinical operations, data management, biostatics, regulatory, quality, manufacturing and medical affairs. - Performs proactive safety monitoring and signal detection for assigned products and presents the findings to cross-functional team and safety governance meetings. - Authors signal assessment report as part of signal detection process, develop safety monitoring plan and pharmacovigilance plan as required. - Manages cross-functional safety management team for the assigned product(s). - Authors safety risk management plan for products under clinical development and post-marketing. - Authors safety sections/modules for BLA/MAA submission dossier (SCS, ISS, Clinical overview). - Oversight on the activities related to the periodic reports preparation (DSUR) in collaboration with the assigned external vendor(s). - Authors and/or reviews documents or sections of key documents as they relate to safety and safety monitoring (e.g.: protocols, protocol amendments, Investigator Brochures, Informed Consent Forms etc.). - Authors and/or reviews section of key CRO documents as they relate to safety and safety monitoring (Safety Management Plan, Medical Monitoring Plan, SAE Reporting, Communications plan, etc.). - Contribute to the development and revision of safety surveillance & risk management SOPs, template. - Collaborate with PV Operation team on medical review of ICSRs and clinical study team on safety surveillance deliverables for the assigned product. - Participate in PV audit and inspections. Qualifications - Excellent verbal and written communication skills. - Excellent interpersonal and customer service skills. - Excellent sales and customer service skills. - Excellent organizational skills and attention to detail. - Excellent time management skills with a proven ability to meet deadlines. - Strong analytical and problem-solving skills. - Proficient with Microsoft Office Suite or related software. - Degree in life science (pharmacy, nursing or MS in health related field). - Advanced degree in epidemiology (desired). - At least 10 years of experience from pharmaceutical/biotech companies predominantly in safety surveillance and safety risk management. - Prolonged periods of sitting at a desk and working on a computer. Benefits - The base salary for this position is expected to range between $219,606.00 - $268,408.00 USD per year. - 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. Company Description 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.

• Delivers effective, accurate and consistent communication to management, internal teams, external clients and vendors. • Stays informed on new industry fraud trends by reviewing external sources that detail industry alerts, outside Financial Institution trends and industry expert evaluations. • Maintain knowledge of fraud and risk applications and systems supported by Velera. • React to change productively and handle other essential tasks as assigned. • Provide training, quality and assurance standardization and ensure deployed across all of Risk Solutions divisions. • Prepare well-written reports cleared within report issuance guidelines and effectively communicate throughout the project lifecycle. • Represent Risk Engagement Enterprise on committees and teams as assigned. • Provide advisory support to the development and ongoing maintenance of proactive and effective controls in the Risk Engagement infrastructure to mitigate risks to an acceptable level.

Role Description The Central Monitor (CM II) will perform remote patient data review activities for Phase I-IV clinical research and/or non-interventional studies (NIS) to assess compliance with the protocol, ICH-GCP, and/or all applicable local and federal regulatory requirements. The CM II will also ensure patient safety and data integrity using a variety of technologies. Performs all tasks routinely and independently, seeking guidance as needed. - Reviews and understands protocol, critical data and process, safety, and data integrity risks related to protocol execution. - Reviews patient data listings and visualizations via analytical dashboards and/or reports to confirm eligibility, identify protocol deviations, patient safety concerns, data integrity issues and illogical/inaccurate/missing data. - Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. - Immediately communicates/escalates serious issues to the project team and with guidance develops action plans. - Documents observations noted during reviews and writes queries, protocol deviations or action items as necessary in appropriate systems for action by sites, CRAs or other functional team members. - Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. - Accesses vendor systems or reports to verify the IP has been dispensed and administered to subjects/patients according to the protocol, that laboratory and other procedures have been performed, that eTMF data is current and complete. - Documents completion of activities via tracking, reporting and/or other required project documents as per SOPs and Monitoring Plan. - For assigned activities, understands project scope, budgets, and timelines; manages patient- and site-level activities to ensure project objectives, deliverables and timelines are met. - Must be able to quickly adapt, with the oversight of the Lead CRA/LCMDA, to changing priorities to achieve goals/targets. - Prepares for and attends Investigator Meetings and/or sponsor meetings. Participates in project staff meetings, as applicable and attends clinical training sessions according to the project specific requirements. Qualifications - Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience. - Knowledge of Good Clinical Practice/ICH E6 (R2) Guidelines and/or other applicable regulatory requirements. - Must demonstrate good computer skills and be able to embrace new technologies. - Mastery of MS Excel (sorting, filtering, calculating, pivoting). - Proficient with Analytical Data Visualization Tools (adjusting visualizations, selecting subsets of data to analyze). - Excellent verbal and written communication skills to relate to internal stakeholders. Able to inform, influence and communicate cross-functionally. - Strong analytical skills. - Developing therapeutic expertise. - <10% travel (limited to trainings, investigator meetings). Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.