Lauren Bateman Email & Phone Number
Who is Lauren Bateman? Overview
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Lauren Bateman is listed as Senior Manager, Regulatory Science, Policy, and Intelligence at CSL, a with 14770 employees, based in Annapolis, Maryland, United States. AeroLeads shows a matched LinkedIn profile for Lauren Bateman.
Lauren Bateman previously worked as Senior Informatics Advisor at Fda and Project Manager - Office of Combination Products at Fda. Lauren Bateman holds Bachelor Of Science (Bs), Biology/Biological Sciences, General from University Of Maryland College Park.
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About Lauren Bateman
Senior Informatics Advisor in the Office of the Chief Medical Office at the U.S. Food and Drug Administration experienced developing and implementing comprehensive technology solutions that foster cross-agency collaboration, enable data-sharing, and ultimately accelerate the path to breakthrough therapeutic and diagnostic options for patients and clinical care providers, and better mechanisms to enhance and promote public health.
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Lauren Bateman work experience
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Role listed
Senior Informatics Advisor
The Office of the Chief Medical Officer (OCMO) (formerly the Office of Clinical Policy and Programs (OCPP)) in the Office of the Commissioner promotes safe, effective and innovative medical products for patients through agency-wide collaboration on combination products, ethical conduct of clinical research, orphan product development, patient engagement and pediatric therapeutics.
Project Manager - Office Of Combination Products
- Combination Product Postmarketing Safety Reporting Dashboard Development: responsible for the full project life cycle of the development of a dashboard solution with Qlik Sense technology to inform the work of FDA’s safety evaluators and reviewers. - Cross-Center Working Group Lead: Leads and manages a multiple cross-Center working groups tasked with streamlining procedures in the 3 medical product Centers to create consistency and efficiency, and fosters collaboration across representatives from the Centers to reach consensus on unified procedures.- Combination Products Annual Performance Report to Congress: Spearheads the development of the annual report to Congress on the activities and impact of the Office of Combination Products during each fiscal year. - Serves as the Office’s technical point of contact for information technology data calls, and represents OCP and the Office of Clinical Policy and Programs in ongoing Agency IT modernization efforts.- Develops project work plans including explanations of the business needs for the projects, the project milestone schedule, stakeholders/beneficiaries, risks and risk mitigation strategies, project metrics, and other project information.- Represents FDA at public meetings, workshops, webinars, and conferences by preparing and delivering presentations, serving on panels, and engaging external stakeholders.
Project Manager - Office Of Clinical Policy And Programs
Accomplishments include:- Stood up the Office of Patient Affairs Patient Listening Session program and published FDA’s Staff Manual Guide 9006- Responsible for planning 9 external public meetings and conferences between 2016 and 2020, each of which had 200+ in person attendees and 500+ web attendees
Senior Associate
Project Manager, Food and Drug Administration (FDA), Office of Clinical Policy and Programs (formally the Office of Medical Products and Tobacco) - Provided leadership and direction related to the planning, development, and execution of cross-cutting regulatory programs and policies that are critical to the public health mission of the FDA. Programs include:• Combination Products Review Program• Orphan Products Development Program• Internal and External Conferences and Meetings- Evaluated methods to improve the effectiveness and efficiency of program operations.- Managed expectations, presenting viable working solutions to overcome resistance and other barriers to change. - Mitigated negative impact through the creation of effective planning strategies and risk assessments. - Performed all duties in compliance with Health and Human Services Enterprise Performance Lifecycle (EPLC) IT governance.- Managed multiple competing priorities and demanding workloads under rigorous timelines. - Ethical, calm under pressure, comfortable with responsibility and accountable in challenging situations.
Treatment Plan Coordinator
- Analyzed appointment schedule, laboratory production, and patient satisfaction to draw conclusions regarding center efficiency and productivity recommendations. - Increased revenue by designing, implementing, and managing employee task management system used to synchronize schedules across center branches.- Responsible for center communication and the development of company newsletter. Created, distributed, and monitored customer satisfaction surveys. - Supervised site schedules based on constraints such as laboratory requirements, procedure urgency, and doctor capabilities. Efficiency results and suggestions were reported to the center manager.- Informal supervisor ensuring coworker’s daily tasks, expectations, and deadlines are met.
Exercise Physiologist
- Designed and implemented work simulation programs based on a patient's injury and job description using a customized Excel document.- Documented assessments of the patient’s daily visits and trending results towards the rehabilitation goal. - Communicated status and progress to referring medical practitioner with immediate escalation as needed. - Delivered detailed oral and written status reports including plans of action to supervisor.
Physical Therapy Aide
- Instructed patients in therapeutic activities and tracked their progress to their individual plan.
Science Education Specialist
- Led scientific programs and shows open to the public.- Researched maritime information in order to develop interactive activities for museum exhibits. - Conducted outreach programs involving traveling to venues to perform shows.
Colleagues at CSL
Other employees you can reach at fda.gov. View company contacts for 14770 employees →
Joseph Quander
Colleague at CslWashington Dc-Baltimore Area, United States
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Taiye Oladipo, Pmp, Mph
Colleague at CslCollege Park, Maryland, United States
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Paul Hart
Colleague at CslWashington Dc-Baltimore Area, United States
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Durga Chouhan
Colleague at CslIndore, Madhya Pradesh, India
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Martin White
Colleague at CslLaurel, Maryland, United States
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Anna Mielech
Colleague at CslUnited States
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Brantley Dorch
Colleague at CslWashington, District Of Columbia, United States
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Ramon Hernandez
Colleague at CslUnited States
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Phil Woodward
Colleague at CslMilford, Ohio, United States
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Duyen Mach
Colleague at CslSilver Spring, Maryland, United States
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Lauren Bateman education
Bachelor Of Science (Bs), Biology/Biological Sciences, General
Master’S Degree, Biodefense
Frequently asked questions about Lauren Bateman
Quick answers generated from the profile data available on this page.
What company does Lauren Bateman work for?
Lauren Bateman works for CSL.
What is Lauren Bateman's role at CSL?
Lauren Bateman is listed as Senior Manager, Regulatory Science, Policy, and Intelligence at CSL.
Where is Lauren Bateman based?
Lauren Bateman is based in Annapolis, Maryland, United States while working with CSL.
What companies has Lauren Bateman worked for?
Lauren Bateman has worked for Csl, Fda, Drt Strategies, Clearchoice Dental Implant Centers, and Atlantic Orthopaedic Specialists.
Who are Lauren Bateman's colleagues at CSL?
Lauren Bateman's colleagues at CSL include Joseph Quander, Taiye Oladipo, Pmp, Mph, Paul Hart, Durga Chouhan, and Martin White.
How can I contact Lauren Bateman?
You can use AeroLeads to view verified contact signals for Lauren Bateman at CSL, including work email, phone, and LinkedIn data when available.
What schools did Lauren Bateman attend?
Lauren Bateman holds Bachelor Of Science (Bs), Biology/Biological Sciences, General from University Of Maryland College Park.
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