Amanda Daugherty

Amanda Daugherty Email and Phone Number

Leawood, KS, US
Amanda Daugherty's Location
Leawood, Kansas, United States, United States
Amanda Daugherty's Contact Details

Amanda Daugherty work email

Amanda Daugherty personal email

n/a
About Amanda Daugherty

Amanda Daugherty is a TMF Study Owner at Phlexglobal, A PharmaLex Company. She possess expertise in clinical research, microsoft office, microsoft excel, microsoft word, healthcare and 1 more skills.

Amanda Daugherty's Current Company Details
Phlexglobal, A PharmaLex Company

Phlexglobal, A Pharmalex Company

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TMF Study Owner
Leawood, KS, US
Amanda Daugherty Work Experience Details
  • Phlexglobal, A Pharmalex Company
    Tmf Study Owner
    Phlexglobal, A Pharmalex Company
    Leawood, Ks, Us
  • Phlexglobal, A Pharmalex Company
    Tmf Study Owner
    Phlexglobal, A Pharmalex Company Feb 2022 - Present
  • Ampd Coolers
    Business Owner
    Ampd Coolers Sep 2021 - Present
    Lees Summit, Missouri, United States
  • Iqvia
    Site Activation Manager
    Iqvia Dec 2020 - Feb 2022
    Overland Park, Kansas, United States
    Direct and manage the delivery of all required start-up, maintenance and regulatory activities for selected studies or multiprotocol programs as determined by either the agreed algorithm or the Sponsor's requirements, including pre-award activities, oversight of the scope of work, budget and resources.
  • Iqvia
    Regulatory & Start Up Specialist I
    Iqvia Nov 2018 - Dec 2020
    Overland Park, Kansas
    Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.Distribute completed documents to sites and internal project team members.Prepare site regulatory documents, reviewing for completeness and accuracy.Review, prepare and negotiate site contracts and budgets with sites.Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.Review and… Show more Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.Distribute completed documents to sites and internal project team members.Prepare site regulatory documents, reviewing for completeness and accuracy.Review, prepare and negotiate site contracts and budgets with sites.Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.Review and provide feedback to management on site performance metrics.Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.Inform team members of completion of regulatory and contractual documents for individual sites.Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics ICF and IP Release documents, in line with project timelines.Provide local expertise to RSU leads and Project team during initial and on-going project timelines planning.Perform quality control of documents provided by sites.May have direct contact with sponsors on specific initiatives.May perform Site Selection Visits if a trained monitor.May participate in feasibility and/or site identification activities Show less
  • Iqvia
    Sr. Clinical Trials Assistant
    Iqvia Aug 2015 - 2018
    6700 W. 115Th St. Overland Park, Ks.
    Clinical Lead (CL), Clinical Research Associates (CRAs)/Project Lead (PL) and Regulatory and Start-up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and stadard operating procedures. Assist with periodic review of study files for… Show more Clinical Lead (CL), Clinical Research Associates (CRAs)/Project Lead (PL) and Regulatory and Start-up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and stadard operating procedures. Assist with periodic review of study files for completeness.Assist CL/PL, CRAs and RSU with prepartion, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.May perform assigned adminstrative tasks to support team members with clinical trial execution. Show less
  • University Of Kansas Medical Center
    Patient Service Representative
    University Of Kansas Medical Center Jun 2012 - Aug 2015
    3901 Rainbow Blvd. Kansas City, Ks.
    Schedule, Cancel, and Reschedule appointmentsAnswer phones, direct calls where needed, take messages and deliver themCollect copaymentsCollect and prep patient chartsScan all outside records into Image NowCollect patient data and enter accordingly into IDX and DSIAssist nurses, medical assistants, and doctors
  • Statewide Public Safety
    Security Officer
    Statewide Public Safety Feb 2011 - Feb 2013
    Kansas City, Missouri Area
    Serve the community I patrol.Assist other officers.Safe guard lives and the property of the accounts.Write reports
  • Jackson Country Sheriffs Office
    Deputy
    Jackson Country Sheriffs Office Oct 2011 - 2011
    Lees Summit, Missouri
     Serve the community I patrol. Safe guard lives and property. Assist other officers Write reports.
  • Centerpoint Medical Center Of Independence, Llc
    Registrar
    Centerpoint Medical Center Of Independence, Llc Jul 2009 - Oct 2010
    Independence, Mo.
    Assisting the patient with anything they need.Collecting all of the information needed from a patient for billing.Enter all information into a Meditech.Assisting Doctors and Nurses with patient information needed.Collect co pays.Admit patients to different levels of the hospital.Answering phones and forwarding the calls.
  • Walgreens
    Photo Technician
    Walgreens May 2008 - Jul 2009
    Independence, Mo.
    Assisting the customer with anything the need.Assisting the customers on the phone.Entering customer’s information into the Walgreens Picture Care Plus Program.Printing the photos on a Fuji 340 Frontier printer.Ringing up the customers orders on the cashier and exchanging the money.Cleaning the photo and film machines.
  • Spine Center
    Receptionist
    Spine Center Apr 2007 - Jan 2008
    Lees Summit, Mo.
    Answering phones.Scheduling appointments.Filing patients foldersInsurance verification.Assist the doctor

Amanda Daugherty Skills

Clinical Research Microsoft Office Microsoft Excel Microsoft Word Healthcare Hospitals

Amanda Daugherty Education Details

  • Metropolitan Community College-Blue River
    Metropolitan Community College-Blue River

Frequently Asked Questions about Amanda Daugherty

What company does Amanda Daugherty work for?

Amanda Daugherty works for Phlexglobal, A Pharmalex Company

What is Amanda Daugherty's role at the current company?

Amanda Daugherty's current role is TMF Study Owner.

What is Amanda Daugherty's email address?

Amanda Daugherty's email address is am****@****via.com

What schools did Amanda Daugherty attend?

Amanda Daugherty attended Metropolitan Community College-Blue River.

What skills is Amanda Daugherty known for?

Amanda Daugherty has skills like Clinical Research, Microsoft Office, Microsoft Excel, Microsoft Word, Healthcare, Hospitals.

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