Sr. Clinical Trial Manager at Takeda Pharmaceuticals
Greater Chicago Area
• Fifteen years of Research experience with extensive focus on clinical trial monitoring and management in accordance with ICH/GCP guidelines and global SOPs/WPDs to meet timelines and deliverables • Seven years of Medical Practice experience as a physician with in-depth understanding of scientific process, medical and statistical concepts • Scope of experience spans wide range of clinical...
• Fifteen years of Research experience with extensive focus on clinical trial monitoring and management in accordance with ICH/GCP guidelines and global SOPs/WPDs to meet timelines and deliverables • Seven years of Medical Practice experience as a physician with in-depth understanding of scientific process, medical and statistical concepts • Scope of experience spans wide range of clinical research function: identification of quality investigator, study start up, study maintenance, study close-out, critical adjudication case review, risk management, study and team managment, and strategic leadership for clinical team and site • Key advisor and partner to upper management connecting their needs to an actionable development plan • Proved management skills: cross-functional coordinating, team building and one-on-one training, work tool creating and work supporting, professional meeting presenting, and new collaboration developing • High level of performance with consistent excellent work metrics Specialties: RESEARCH: ICH Guidelines/GCP Expertise and SOP Implementation; FDA and Quality Assurance Audits; Phase II, IIIa, IIIb, IV Studies; Source documentation Verification; Monitoring Reports; Safety review; Adjudication case review; investigator Meetings; Investigator recruitment and assessment. MANAGEMENT: Cross-functional coordinating & budget control, Team building and one-on-one training, Work tool creating and work support, Professional meeting presenting & new research cooperation developing.Sr. Clinical Trial Manager @ Manage clinical study/studies according to global regulatory requirements and SOPs, and support clinical strategy defined in Clinical Study Plan. From December 2014 to Present (1 year 1 month) Ming Jing is skilled in: Clinical Trials, GCP, Sop, Protocol, Clinical Monitoring, ICH-GCP, Clinical Research, CTMS, CRO, Diabetes
Manage clinical study/studies according to global regulatory requirements and SOPs, and support clinical strategy defined in Clinical Study Plan. Manage clinical study/studies according to global regulatory requirements and SOPs, and support clinical strategy defined in Clinical Study Plan.
What company does Ming Jing work for?
Ming Jing works for Takeda Pharmaceuticals
What is Ming Jing's role at Takeda Pharmaceuticals?
Ming Jing is Sr. Clinical Trial Manager
What industry does Ming Jing work in?
Ming Jing works in the Pharmaceuticals industry.
Who are Ming Jing's colleagues?
Ming Jing's colleagues are Sarav Narayanan, Tom P.E., Danielle Catanese-Chack, David Bailey, Sue MBA, Ilonka Ivanova, Susanne Winkel-Nellen, Sigurd Okkels, Holger Dittberner ., and Dr. Metzinger
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