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Pharmacy Technician Mission Viejo

Location:
Mission Viejo, CA
Posted:
July 18, 2024

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Resume:

Sarvenaz Shahrad Bejestani

***** ****** ***** *** ******* Viejo, CA, 92692 **************@*****.*** 617-***-**** SUMMARY OF QUALIFICATIONS:

• Highly motivated PharmD student known for exceptional reliability and meticulous work ethic.

• A dedicated learner with a keen passion for acquiring new skills and delivering top-notch results.

• Skilled at using pharmacy management software, and electronic health record system.

• Expert in pharmacokinetics, optimizing drug therapy through personalized dosing and therapeutic drug monitoring.

• Experienced in vaccine administration and patient education.

• Fluent in English and Persian.

EDUCATION

Massachusetts College of Pharmacy Boston, MA

Pharm-D Degree Graduated: May 2024

Relevant Clinical Rotations: Amazon Pharmacy, Cerritos Hospital Pharmacy, Rite Aid Pharmacy, UMASS Memorial Hospital Infectious Disease. Certifications:

CA & MA Pharmacist Intern License MTM Certificate CITI Certificate Heartsaver Blood Born pathogen Diabetes Certificate BLS Certificate RELATED EXPERIENCE

CVS Pharmacy Northborough, MA

Pharmacy Technician/ Intern Oct. 2021- Present

• Prepare and dispense patient medications accurately and efficiently.

• Collaborate with other pharmacists to ensure patient safety and adherence.

• Counsel patients on medications and identify potential drug interactions.

• Utilize technology for maintaining patient records and inventory management. Massachusetts General Hospital Boston, MA

Patient Coordinator Dec. 2020- July. 2021

• Entered and verified patient information in the system.

• Provided support to patients and healthcare providers.

• Developed strong interpersonal skills and attention to patient needs. Privo Technologies Peabody, MA

Lab Assistant Jan. 2019- July. 2020

• Experienced in conducting clinical trials and navigating FDA approval processes

• Executed experiments following protocols, recording data accurately.

• Managed rejected samples and documented them in appropriate logbooks.

• Contributed to drug manufacturing process for FDA-approved clinical trials.

• Implemented new quality control (QC) guidelines for enhanced efficiency.



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