Taizoon Khokhar Email & Phone Number

Irving, Tx, Us

Specializing in oncology, it caters to the biotech, CRO, CDMO, Pharmaceutical Industries, and the Medical Education sector. Expertise in drug development, clinical operations, and medical education is leveraged to provide strategic solutions that foster business growth, operational efficiency, and product innovation. • Spearheads the development and execution of comprehensive medical education initiatives, conference-style learning sessions, and advanced standards of care. Introduced new industry advancements and challenges to key opinion leaders (KOLs) and practicing physicians, akin to impactful strategies employed by organizations. • Streamlines API and clinical trial product manufacturing processes; advises on drug development to enhance efficiency, avoid delays, reduce compliance costs, and minimize goods loss. Focus on maximizing product yield by reducing redundant QA and stability holds, exclusively targeting clinical trial material production. Provide tactical support to navigate manufacturing challenges, ensuring strategic objectives are met with cost-effective, quality-focused strategies.• Drives services and product development initiatives, leveraging a unique blend of operational, clinical, and technological expertise to deliver innovative solutions that meet the industry's dynamic needs. • Implements and optimizes processes, developing regulatory and compliance strategies that ensure adherence to industry regulations while facilitating efficient project execution. • Establishes SOPs and a quality system foundation, providing a robust framework for operational excellence and continuous improvement across client organizations.

Plano, Texas, Us

Led strategic direction, oversaw operational excellence, and drove innovation aligned with corporate goals. Executed visionary leadership to steer company-wide growth, ensuring competitive positioning and stakeholder value enhancement.• Directed trial budgets, expenses, and patient accrual with strategic financial measures, ensuring trials stay on schedule. Achieved significant cost savings of ~20%, keeping operations well under the trial budget, optimizing technology solutions, and demonstrating efficient progress within financial constraints.• Drove strategic growth for DAVA, leading to a 60% revenue increase through meticulous planning, efficient execution , and integration of staffing and budgeting, aligning with client objectives and industry standards for resource optimization.• Led the development and execution of specialized peer-to-peer learning workshops and medical education conferences, markedly boosting clinical trial accrual by educating doctors and research teams on the benefits of trials for patient care. Also, drove the advancements in clinical trial methodologies and enhanced professional knowledge across the trial participants.• Spearheaded over 1,000 trail acceleration workshops, benefiting over two dozen companies and boosting patient accrual in more than three dozen trials, resulting in early or on-time trail completion.• Developed and enforced SOPs and quality assurance backbone, establishing rigorous operational integrity and regulatory compliance protocols.• Innovated in services and product development, overseeing the launch of new offerings and enhancement of existing products.• Spearheaded staff planning and developed team growth strategy, aligning with HR policies to foster a culture of excellence and collaboration• Led development of customized processes using available technology infrastructure, streamlining operations and bolstering efficiency.

• Led global expansion initiatives for clinical trials, entering 10+ new markets, including Europe, the UK, China, and others, significantly increasing product reach. Established office in India to support round-the-clock operations, enhancing global workforce presence without direct sales figures involvement.• Championed API/Biologics manufacturing and product development, strategically setting up new vendor relationships to streamline manufacturing and quality approval processes, reducing costs significantly and enhancing scalability to support global trials and pre-NDA work. Achieved substantial cost savings in both API and tablet manufacturing, resulting in operations well under budget.• Directed trial budgets, expenses, and patient accrual with strategic financial measures, ensuring trials stay on schedule. Achieved significant cost savings of ~20%, keeping operations well under the trial budget, optimizing technology solutions, and demonstrating efficient progress within financial constraints.• Developed and enforced SOPs and quality assurance backbone, establishing rigorous operational integrity and regulatory compliance protocols.• Designed and implemented workflows and processes for data collection, ensuring regulatory compliance and efficient trial management.• Executed resource and operation budget planning, laying financial groundwork for operational efficiency and project feasibility.• Spearheaded staff planning and developed team growth strategy, aligning with HR policies to foster a culture of excellence and collaboration.• Identified and integrated a full range of systems for various aspects of clinical research, focusing on cloud-based infrastructure to enhance scalability and operational flexibility.• Led development of customized processes using available technology infrastructure, streamlining operations and bolstering efficiency.

Us

Masters, Masters Of Biotechnology

Certificate In Business, Business Management

Bachelor Of Science (B.Sc.), Zoology/Animal Biology

Diploma In Medical Laboratory Technology, Clinical Laboratory Science/Medical Technology/Technologist