Phoebe Mathew

About Phoebe Mathew

With over 14 years of experience in clinical trials, I am currently a Local Trial Manager at Amgen. My expertise spans roles in industry and academic settings, including leading the IBD Registry at CorEvitas and managing oncology trials at DOCS Icon for study start-up. I hold a Master of Science in Public Health and am pursuing a Master of Biomedical Sciences. I am passionate about enhancing patient outcomes through dedicated clinical research.I bring a collaborative mindset to my work, partnering closely with directors and leads to set targets for clinical monitoring staff and ensure that trial recording aligns with project objectives, particularly during study start-up and maintenance phases. I am adept at creating and implementing study-specific clinical monitoring tools and documents. As a representative, I have been instrumental in recording and sharing interactions with clients. My skills include recruiting staff, training personnel, and directing cross-functional teams to achieve both short- and long-term goals. I am recognized for my excellent communication and presentation skills, and my ability to organize and motivate others.Areas of expertise include: Women\'s Health Oncology: Breast, Lung, Heme, Bladder, Prostate, Renal, Head, Laryngeal, Oral Cavity, Pharyngeal, Thyroid, Head and Neck Nutrition Weight Loss Dental and Oral Health Inflammatory Bowel Disease (Gastroenterology)

Experience

1. Local Trial Manager (Early Phase Development - Fast Lane Oncology)

   Amgen

   Jun 2022 — Present · Thousand Oaks, CA, US

   Provide Clinical Trial Management with a focus on site activation and ongoing study management in clinical trials related to oncology head and neck-related studies with limited guidance.• Utilize advanced skills in Veera Vault, trello, eclinical, adverra IRB, tableau, spotfire and iMedidata platforms to manage and maintain essential study documents and data, ensuring compliance with regulatory requirements.• Proficient in report management, including generation, review, and submission of study reports to relevant stakeholders.• Stay up to date with industry trends and regulatory changes, incorporating best practices into study management and ensuring adherence to applicable guidelines and standards.• Foster strong relationships with investigative sites, vendors, and key stakeholders to optimize study collaboration and drive efficient study execution.• Actively participate in cross-functional meetings and contribute to the development of study protocols, study plans, and other study-related documents.• Provide guidance and mentorship to junior team members, promoting professional growth and ensuring high-quality performance.• Contribute to the development and improvement of standard operating procedures (SOPs) and processes, promoting operational excellence and continuous improvement.

Education

• Penn State University

  Bachelors of Science in Premedicine, Minor in Psychology

• Arcadia University

  Master of Science, Public Health

  2014 — 2016