Exec Dir Regional Clinical Monitoring

What You'll DoLead regional CM staff for high-quality site management and monitoring of clinical trialsServe as senior internal CM contact for engagement with other company leaders and client representativesProvide strategic direction for the function in the region in concert with CM's global functional vision and strategyCollaborate with CTI cross functional leaders to ensure monitoring practices work effectively with processes and procedures followed by other teams and geographiesMeet regularly with the VP of Global Clinical Monitoring and global peers to share relevant updates, address challenges, and formulate shared solutionsDrive process improvement for CM performance, quality, and efficiency in regionAlign with and make sure delivery is aligned with operational, productivity, and financial metrics, including adherence to trial budgets and time tracking expectationsOversee new CM processes and CTI initiatives to boost regional performance and profitabilityUtilize Business Intelligence (BI), KPIs, and metrics to monitor trends, mitigate risks, and support trial and personnel successLead discussions to refine procedures that improve monitoring quality and efficiency in a manner that facilitates greater efficiency and effectiveness across CTI's trial functionsPartner with Quality Assurance and other departments to update and maintain CM SOPs, keeping them current with CTI and industry advancementsParticipate in trial team meetings, sponsor meetings, and client governance discussions to provide guidance and oversightLead by example in supporting staff development, career path planning, and organizational growth within the regionProvide feedback to CRA Management for consistent policy and performance management implementationCollaborate with HR on talent acquisition and candidate evaluation, using every opening as an opportunity to elevate the talent of the organizationWork with the Resource Management Group to allocate trial personnel within the region for optimal delivery on trial and general resource utilizationRepresent CM in bid defenses and strategic discussions for new business opportunitiesContribute to the development and review of RFPs and budgets for trialsEnsure timely escalation of CM issues to executive leadershipEnsure consistent monitoring quality and adherence to applicable regulations and best practices across the regionOversee CRA assessment visits and ensure feedback is communicated to relevant stakeholdersIdentify actions for monitoring trends resulting in CAPAs and quality concerns for the regionWhat You BringDemonstrate exceptional leadership to create a positive, cross-collaborative work environment that fosters a culture of excellence through staff support, training, engagement, mentorship and innovationSuccessful track record in supervising, mentoring, and coaching teams on a large scale (i.e., over 100 team members)Demonstrate financial acumen and ability to manage study and department budgetsDemonstrate competency in leading cross-functional process improvement effortsStrong computer skills to include MS Office (Word, Excel, PowerPoint) and ability to effectively utilize trial systems to positively impact effective trial managementAbility to work in fast-paced, cross-border, multi-cultural environment with several competing prioritiesDemonstrate extensive knowledge of global regulatory requirements (GCP/ICH) related to trial management in assigned geographical regionsAble to interpret and analyze CTI financial reports at both study and regional levels, providing leadership to clinical monitoring teams to achieve financial goals at both the trial and departmental levelAt least 15 years of experience in pharmaceutical / biotechnology field, with progressive positions in Clinical MonitoringBachelor's degree in allied health fields such as nursing, pharmacy or health science, preferably with clinical trial management experience or an equivalent combination of education and relevant work experienceExperience with use of clinical systems (Clinical Trial Management System [CTMS], electronic data capture [EDC], electronic Trial Master File [eTMF], etc.) used in clinical trials and process improvement surrounding use of technology to improve efficienciesWhy CTI?We support career progression - 25% of our global staff is promoted annually and we have a structured mentoring program to provide the support you need to move forwardWe value education and training - We provide tuition reimbursement, partner with universities and colleges to create programs in our field, and have a dedicated training departmentWe value our people - We have never had a layoff in our 20-year history, support a work-life balance with flexible schedules, and have provided cash bonuses every year for the past decadeOur culture is unparalleled - Click here to learn more about "The CTI Way"We think globally and act locally - We have a global philanthropic program supporting our team's efforts to improve their local communities (Click here to learn more about our "CTI Cares" program)Important NoteIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.Please NoteWe will never communicate with you directly via Microsoft Teams Messaging or text messageWe will never ask for your bank account information at any point during the recruitment processEqual Opportunity Employer/Veterans/DisabledEqual Opportunity Employer/Protected Veterans/Individuals with DisabilitiesThis employer is required to notify all applicants of their rights pursuant to federal employment laws.