Summary
Overview
Work History
Education
Skills
Languages
Timeline
Generic
AMEL NINOUCHE

AMEL NINOUCHE

Clinical Research Coordinator Endeavor Health
Evanston,IL

Summary

CLINICAL RESEARCH PROFESSIONAL with combined academic and professional experience in good clinical practice (GCP), research methodologies, HIPAA compliance, good document practice, GLP and GMP, CITI program certification, EPIC, Quadrilingual.

Overview

9
9
years of professional experience

Work History

Clinical Research Coordinator

Endeavor Health
Evanston, IL
06.2024 - Current
  • Provides clinical care services including consenting, treating and monitoring of patients.
  • Conduct Screening visits.
  • Ship lab samples.
  • Dispense research drug to patients according to protocol.
  • Perform a variety of research, data entry and regulatory duties of a routine and technical nature related to departmental research endeavors.
  • Ensure adherence to protocols and quality of information received.
  • Assist with budget proposals and study budget tracking.
  • Ensure compliance with local, state and federal regulations for the protection of human subjects.
  • Complete regulatory submissions, revisions for the Institutional Review Board (IRB).

Clinical Research Analyst I, Research Analyst II

Charles River Laboratories
Skokie, IL
07.2022 - 05.2024
  • Utilize workflow software to assign and manage research projects.
  • Perform analysis of complex laboratory assays based on protocols and in full compliance with SOPs and GLP regulations.
  • Independently and with minimal error use Genetic & In Vitro Toxicology main platforms: Z2 Coulter Counters, Cellaca viable cell counters, Canto, Fortessa,and MACSQuant flow cytometers
  • Record data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.
  • write correspondence, deviations, and notes to file for studies and laboratory related activities to a high level and in a concise manner. Communicate clearly orally and in a written format using correct grammar and syntax.
  • Independently and with minimal error, perform dosing of studies.

Clinical Research Analyst, Contract

Kelly Services
Skokie, IL
01.2022 - 07.2022
  • Performed analysis of moderately complex laboratory assays based on protocols and in compliance with SOPs and GLP regulations.
  • Record project data in accordance with GLP regulations.
  • Set up basic laboratory equipments and instrumentation with guidance from senior technical staff.
  • Performed all other duties as assigned.

Quality Control Technician/Chemist

Bajaj Medical medical Inc
Chicago, IL
01.2021 - 07.2021
  • Assist quality control supervisor by performing analysis tests on the raw and finished product, recording results, notify supervisor and production of adjustments as needed, and retest.
  • Inspect products for proper color, texture, labels, code, lot number, and proper seals, torque, weights, etc... and notify the line supervisor if any adjustment is needed.
  • Review batch records for production and packaging records for the lines.
  • Perform daily calibration of instruments, balances, and ph meter, including annual calibration of FTIR and UV visible.
  • Water sampling for visual inspection and sending out for micro testing.
  • HPLC, and GC, FTIR, and UV visible analysis of finished products, raw materials, and washing samples.
  • Update charts for stability chambers, warehouse, and retain room.

Manager

McDonald's
Chicago, IL
07.2015 - 02.2021
  • Assigned tasks to associates to fit skill levels and maximize team performance.
  • Greeted and encouraged feedback from customers to implement in-store operational changes.
  • Trained employees on additional job positions to maintain coverage of roles at all times.
  • Completed daily sales reports and analyzed metrics to identify trends.

Clinical Research Intern

Synexus
Chicago, IL
01.2019 - 01.2019
  • Tended to subjects while maintaining concurrent responsibilities, including monitoring vitals, measuring blood pressure,hemoglobin tests, pregnancy screenings
  • recording patient data in accordance of Good Clinical Practice (GCP) and Good Document Practice (GDP).
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting.

Education

Clinical Research Professional -

Clinical Fastrack Program
Oak Brook, IL
03.2019

1 year Master of Science (MS) - Biotechnology

The University of Béjaïa

Bachelor of Science (BS) - Biology

The University of Béjaïa

Skills

  • Sampling protocols
  • Inspection procedures
  • Team management
  • Customer service
  • Analytical mindset
  • Star communicator

Languages

English | French | Berber and arabic

Timeline

Clinical Research Coordinator

Endeavor Health
06.2024 - Current

Clinical Research Analyst I, Research Analyst II

Charles River Laboratories
07.2022 - 05.2024

Clinical Research Analyst, Contract

Kelly Services
01.2022 - 07.2022

Quality Control Technician/Chemist

Bajaj Medical medical Inc
01.2021 - 07.2021

Clinical Research Intern

Synexus
01.2019 - 01.2019

Manager

McDonald's
07.2015 - 02.2021

Clinical Research Professional -

Clinical Fastrack Program

1 year Master of Science (MS) - Biotechnology

The University of Béjaïa

Bachelor of Science (BS) - Biology

The University of Béjaïa
AMEL NINOUCHEClinical Research Coordinator Endeavor Health