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Start for FreeJoanna Dojillo
Senior Director, Clinical Operations @Nikang Therapeutics Inc
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WORK HISTORY
Senior Director, Clinical Operations @Nikang Therapeutics Inc
US
Accomplished and versatile clinical project leader with 20 years of experience delivering strategic results in execution of early phase domestic and international clinical trials from initial concept (e.g. pre-IND meeting and IND application submission) to completion (e.g. CSR development and EOP2 meeting). Leader of high performing multifunctional teams in drug development projects. Equipped with diverse therapeutic expertise and an entrepreneurial spirit, successfully identified opportunities to implement process improvements to ensure budget management and compliance, while maintaining focus on corporate critical paths. Recognized for exemplary performance, strong communication skills, and unwavering commitment to enhancing quality output to management, teams, and colleagues. •Experience with FDA, IRB/IEC submissions approvals •GCP, QA, GDPR, Regulatory •IND Development •Cross-functional Leadership •Process Development •Financial/Budget Adherence •Vendor Management •Risk Identification/Mitigation •Type FDA B/C Meetings •FDA Fast Track, Breakthrough Therapy, Accelerated Approval •RFP Development •Analytical Problem Solver •Global Product Development •Team creation and management
EDUCATION
The University of British Columbia
Master of Science (M.Sc.), Biology / Chemical Ecology
UC Irvine
Bachelor's of Science, Biology, General
ABOUT JOANNA DOJILLO
As a highly experienced Sr. Director of Clinical Operations my scope of experience extends to operational leadership and coordination in domestic and international Phase clinical trials from initial concept (e.g, IND filing, FDA Type B&C meetings, etc.) to completion. I am highly skilled at mentoring and leading cross-functional high-performing teams in the design and execution of clinical trial projects in accordance with regulatory guidelines and corporate objectives. I possess diverse therapeutic expertise and my background includes working with both small start-up (pre-IPO/virtual companies) to working with large, renowned pharmaceutical companies. My career history demonstrates strengths in strategic planning, development of efficient clinical trial timelines, identifying improvement opportunities to lead highly effective, cross-functional teams and streamline processes to enhance efficiency and performance. I’m a resourceful leader who thrives in fast-paced, milestone-driven environments, and excel in adapting to shifting priorities and changing responsibilities. As a team leader, I encourage a culture of collaboration, open communication, efficiently managing resources, and strengthening systems and procedures in all phases of large-scale clinical projects, while leaning on years of experience for mitigating risks and identifying bottle-neck issues. My strengths in operations management, analysis and identification of inefficiencies, and ability to provide advanced solutions, comes from an innate entrepreneurial sprit and the drive to deliver results that meet or exceed corporate expectations. As a respected and valued professional in every team I\'ve been part of, I’ve been recognized for exemplary performance, strong communication skills, and unwavering commitment to enhancing quality of service provided to teams, colleagues, clients, and stakeholders. People enjoy working with me because of my professional and positive can do attitude, collaborative leadership style, focus on the task at hand, and my excellent interpersonal and communication skills. My many accomplishments can be seen on my resume.
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