Assistant Health Insurance

Jacqueline Jeha

*** **** **** **; Avon, Ma *****

Phone: 401-***-****; e-mail: ******@*****.***

Qualifications Summary

As an integral clinical team member for a small CRO; engaged in all stages of multi-center IDE and IND

studies for submission to domestic regulatory bodies. Background includes clinical research experience in

ophthalmology, diabetes and orthopedics, as well as extensive academic and other healthcare experience in

infectious disease.

Professional Experience

Pleiad. Inc., Cambridge, Ma

June, 2010-December, 2010

Clinical Trial Assistant

• Supported clinical management, site management and monitoring activities from site selection through

study closure for a small international full service CRO.

• Developed, maintained, and periodically audited paper and electronic Trial Master File for multi-center

studies.

• Review and track regulatory, ethics committee and other essential documents for completeness and

accuracy in accordance with regulatory requirements, ICH and GCP guidelines, corporate Standard

Operating Procedures and study specific Work Process Documents.

• Assisted data management in data reconciliation by tracking data clarifications issued and serving as

point of contact for sites and CRAs to coordinate query resolution.

• Liaised between CRAs and sites to ensure that appropriate study supplies, documents and other site

needs were met to effectively execute clinical trial.

• Worked cross-functionally with Central IRBs, Drug Manufacturers and Distributors to ensure timely

shipment of study drug during the start up phase

Providence Veterans Affair Medical Center, Providence, RI

May, 2008- May, 2010

Research Assistant

• Assisted with invitro methodologies including antimicrobial susceptibility testing on Methicillin

Resistant Staphylococcus aureus isolates, using glycopeptide antibiotics for the purpose of measuring

growth response from isolated organisms.

• Responsible for invitro methodology retrospective project set-up, process and results interpretation in lab

notebook.

• Created Standard Operating Procedures for each experiment on antibiotic susceptibility.

• Extensively trained on Health Insurance Portability and Accountability Act (HIPPA)), Investigation

Review Board (IRB) Training for Good Clinical Practices (GCP) and Human Subjects Protection,

Biosafety and Biohazard Training, research Data Security Training, Cyber Security and Ethics

• Managed media preparation, autoclave use, streaking of bacterial cultures, and laboratory material

inventory.

CVS Pharmacy, Pawtucket, RI

May, 2006- May, 2010

Pharmacy Technician

• Applied pharmaceutical knowledge learned in the classroom

• Completed of routine tasks such as, filling prescriptions and data base entry.

• Developed working knowledge of the Health Care Industry and billing insurance.

Rhode Island Department of Health, Providence, RI

May, 2006 –August, 2007

Internship

• Interned with the Chief Board of Pharmacy

• Assisted with the Chief Board of Pharmacy in over a dozen inspections of retail and hospital pharmacies

throughout the state of Rhode Island, attended monthly board meetings, researched information within

other states necessary to implement new technologies such as electronic prescriptions, for the

advancement of pharmacies and pharmacists in the state, compiled and presented facts vital to the board.

• Obtained in-depth knowledge of state laws, industry standard rules, and regulations governing

pharmacies.

Education

Present Masters, Public Health, Estimated graduation August 2011

Brown University, Providence, Rhode Island

Title: Determinates of H1N1 vaccination among school aged children

May 2008 Bachelor of Science, Microbiology

University of Rhode Island, Kingston, Rhode Island

Contact this candidate