Chris Faison work email
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Chris Faison personal email
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As a Principal of Faison Associates, I specialize in providing comprehensive medical writing and review services for Phase 1-4 clinical research programs in the biotechnology and pharmaceutical industries. With over 20 years of experience in the industry, I have a proven track record of delivering high-quality clinical and regulatory documents including protocols, study reports, briefing documents, and eCTD modules across various therapeutic areas.I am committed to contribute to product development by ensuring that all clinical and regulatory documentation is meticulously prepared, clear, and compliant with global and local regulatory standards. Additionally, I source and manage specialized medical writing and quality control teams, offering turnkey solutions that streamline document development processes and enhance operational efficiency.I take pride in my ability to partner with clients to navigate the complexities of clinical and regulatory document development, reduce time-to-market, and ultimately bring much-needed therapies to patients. Whether you need targeted support for a specific project or a full-service solution, I can help drive your clinical development programs forward with quality and efficiency.
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PrincipalSource For Sustainability, Llc (Dba Faison Associates) Jun 2012 - Oct 2024Provide services for Phase 1-4 clinical research programs:-Medical writing and review of clinical submission documents including clinical reserach protocols, Investigator Brochures, Clinical Study Reports, FDA briefing documents, and justification documents. Clinical product development and management expertise in biotechnology and pharmaceutical industries
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Manager, Global Process OptimizationImclone Systems, A Wholly-Owned Subsidiary Of Eli Lilly And Company Jun 2011 - May 2012UsDrove quality and efficiency of clinical trials by tracking key metrics, providing continuous process and quality improvement, and clinical trial systems support and expertise. -
Contractor, Clinical OperationsImclone Systems, A Wholly-Owned Subsidiary Of Eli Lilly And Company Nov 2010 - Jun 2011UsManaged the proper closeout of multiple oncology Phase I & II studies, including trial master file QC and closeout, handling and analysis of pharmacokinetic and pharmacogenomic samples, budgetary reconciliation, and clinical study report writing. Studies investigated the safety and efficacy of novel biologic agents with and without the addition of chemotherapy in multiple tumor types.Managed process development and optimization for the appropriate management of protocol deviations, including prevention and handling.
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Clinical Project ManagerGalderma Jun 2009 - Oct 2010Managed operations for multiple large Phase II & III clinical research studies.
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Clinical Trial ManagerSanofi-Aventis 2000 - 2009Paris, France, FrManaged multiple company- and investigator-sponsored studies for Oncology Medical Affairs. Studies involved novel combinations of biologics and chemotherapies, providing patients with NSCLC more treatment options and targeted therapy. Managed the development of clinical trial protocols, data collection, and quality plans, and was responsible for a budget of over $25 million in combined projects. -
Sustainability PreceptorSanofi-Aventis 2008 - 2008Paris, France, FrWorked on assignment with Sustainable Development group:• Developed content and format of U.S. Sustainability Internet site in compliance with corporate and local communication guidelines• Developed “Socially Responsible Investment Roadshow” materials• Conducted sustainability awareness and education training for employees • Facilitated sustainability partnerships with stakeholders, both internally and externally• Contributed content to and editorial feedback for U.S. Sustainability Reports.
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Clinical Research AssociateIno Therapeutics 1996 - 2000Hampton, Nj, UsParticipated in the development Inhaled Nitric Oxide (iNO), resulting in an FDA approval of iNO therapy for persistant pulmonary hypertension of the newborn. Monitored investigational study sites by auditing data and reviewing regulatory documentation to ensure compliance and data integrity for clinical study report submissions. Conducted study initiation visits, routine monitoring visits, and close-outs.
Chris Faison Skills
Chris Faison Education Details
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Fairleigh Dickinson UniversityManagement -
Kutztown University Of PennsylvaniaEnvironmental Science - Biology
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Madison High School
Frequently Asked Questions about Chris Faison
What is Chris Faison's role at the current company?
Chris Faison's current role is MBA | Principal at Faison Associates | Freelance Medical Writer | Your trusted partner for regulatory medical writing.
What is Chris Faison's email address?
Chris Faison's email address is fa****@****hoo.com
What schools did Chris Faison attend?
Chris Faison attended Fairleigh Dickinson University, Kutztown University Of Pennsylvania, Madison High School.
What are some of Chris Faison's interests?
Chris Faison has interest in Clinical Research, Economic Empowerment, Politics, Oncology, Education, Environment, Poverty Alleviation, Science And Technology, Environmental Conservation, Social Entrepreneurship.
What skills is Chris Faison known for?
Chris Faison has skills like Process Optimization, Sustainable Business, Sustainable Development, Environmental Science, Clinical Trial Management, Cross Functional Team Leadership, Pharmaceuticals, Biotechnology, Pharmaceutical Industry, Ctms, Clinical Trials, Leadership.
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