Erin Majewski

Order Entry Technician at Grane Rx
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Contact Information
us****@****om
(386) 825-5501
Location
Sellersville, Pennsylvania, United States, US
Languages
  • English -

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Bio

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Experience

    • United States
    • Hospitals and Health Care
    • 100 - 200 Employee
    • Order Entry Technician
      • May 2021 - Present

    • Data Entry Technician
      • Aug 2018 - Aug 2022

    • United States
    • Wellness and Fitness Services
    • 700 & Above Employee
    • Pharmacy Technician
      • Mar 2013 - Aug 2022

      - Manage multiple priorities including, but not limited to: entering and filling medications, billing insurance companies, managing inventory levels, and answering and directing phone calls- Problem solve when insurance rejects a claim, or when a prescription is written unclear/incorrectly- Educate patients on aspects such as compliance, safety, and drug disposal - Manage multiple priorities including, but not limited to: entering and filling medications, billing insurance companies, managing inventory levels, and answering and directing phone calls- Problem solve when insurance rejects a claim, or when a prescription is written unclear/incorrectly- Educate patients on aspects such as compliance, safety, and drug disposal

    • United States
    • Hospitals and Health Care
    • 400 - 500 Employee
    • Clinical Research Associate for Pathology
      • Dec 2017 - Aug 2018

      - Manage clinical studies at the Central Testing Lab in collaboration with NSABP- Work with the pathology administrative group, Magee lab staff and management, and the chief of pathology at Magee- Participation on study teleconferences or in-person meetings as necessary- Participation with IRB preparation and submission as needed- Assumes multiple lead roles in protocol implementation and data management- Create an official data-entry protocol- Collect study data and entry into protocol designated database- Knowledge of clinical trial standards and FDA, IRB, and hospital lab guidelines

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Research Technician
      • Nov 2016 - Dec 2017

      - Responsible for the receipt, preparation, and accountability of investigational medications- Maintain compliance with over 450 clinical research protocols and their corresponding documentation o Departments: Oncology, Psychology, Neurology, Pulmonary, Cardiology, Pediatrics, etc. - Communicate and collaborate with clinical research associates, study nurses, and coordinators- Manage drug accountability through shipments, cycle counts, drug inventory logs, patient returns, and IVRS/IXRS/IWRS/IRT systems- Organize study drugs and materials for visiting CRAs- Review incoming protocols for accuracy and clarity- Ensure study files are organized by date and category- Develop training processes and documentations for sterile product preparation per USP<797> and hazardous drug guidelines- Answer and direct phone calls and emails accordingly- Lead employees in sterile preparations- Oversee the environmental monitoring program per FDA/GMP guidelines- Develop a usage plan for sterile stocks to decrease waste and increase profits- Develop and maintain protocols and batch worksheets for sterile and non-sterile compounding- Perform non-sterile compounding per Investigational New Drug (IND) submissions - Adhere to the “Health Insurance Portability and Accountability Act” guidelines

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Biopharmaceutical Manufacturing Associate
      • Aug 2016 - Nov 2016

      - Operate equipment in the downstream production of Tanzeum in a cGMP environment- Responsible for buffer formulations and vessel cleanings (CIP and SIP)- Document all manufacturing activities clearly and accurately with cGMP compliance- Obtain the ability to troubleshoot- Attend daily team meetings to clarify team goals and designate individual tasks - Operate equipment in the downstream production of Tanzeum in a cGMP environment- Responsible for buffer formulations and vessel cleanings (CIP and SIP)- Document all manufacturing activities clearly and accurately with cGMP compliance- Obtain the ability to troubleshoot- Attend daily team meetings to clarify team goals and designate individual tasks

Education

  • University of the Sciences in Philadelphia
    Bachelor's degree in Pharmaceutical Sciences, Pharmaceutical Sciences
    2012 - 2016
  • Pennridge High School
    Highschool Diploma
    1999 - 2012

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