Summary
Overview
Work History
Education
Skills
Timeline
Generic

Christine Fournier

Wareham,MA

Summary

Versatile medical professional knowledgeable in coordinating patient information, laboratory samples and compliance documents for diverse positions. Highly organized and thorough with good planning and problem-solving abilities. Successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.

Overview

25
25
years of professional experience

Work History

Purchasing Supervisor

Northeast Medical Research Associates Inc.
06.2022 - 03.2024
  • Inventory and purchase of site supplies. From daily operations to protocol specific guidelines and equipment. Researching and provide top product to meet needs and most efficient cost for 100% satisfaction
  • Evaluated potential suppliers for reliability, product quality, and delivery timeliness, selecting best options for company needs.
  • Developed inventory management strategies, reducing stock discrepancies and minimizing waste.

Clinical Research Coordinator

Northeast Medical Research Associates, Inc.
04.1999 - 03.2024
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed, and shipped lab specimens.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
  • Multi-task several trials and complete with 100% recruitment/retention and efficiency.
  • Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
  • Trained new team members on essential clinical research protocols and procedures, promoting culture of continuous learning.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
  • Developed and maintained accurate and up-to-date case report forms and source documents.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Oversaw management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
  • Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
  • Reviewed referral information and kept track of intakes from various referral sources.

Education

Certification - Medical Assistant

Fisher College
Boston, MA

Skills

  • Price comparison
  • Material Requirement Planning
  • Supplier Evaluation
  • Vendor Relationship Management
  • Resourcefulness
  • Professional Demeanor
  • Laboratory, Pharmacy
  • IRB, FDA, GCP, ICH
  • EDC, IWRS
  • Documentation Management
  • Patient recruitment/participation
  • Investigational product management
  • Phlebotomy/EKG

Timeline

Purchasing Supervisor

Northeast Medical Research Associates Inc.
06.2022 - 03.2024

Clinical Research Coordinator

Northeast Medical Research Associates, Inc.
04.1999 - 03.2024

Certification - Medical Assistant

Fisher College

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Christine Fournier