Leanna Reddick
RTP,NC
Summary
Leanna Reddick is a Clinical Support Specialist with more than 8 years’ experience in Pharma, as well as 3+ years of laboratory experience. She has experience with clinical data management, generating clinical reports and operating eTMFs. Leanna spent more than 3 years instructing young adults in workforce development at a community college. This opportunity provided her with a depth of knowledge in both the clinical and pharmaceutical sectors.
Overview
4
4
years of professional experience
Work History
CLINICAL SUPPORT SPECIALIST I
08.2021 - Current
- Precision for Medicine
- Provides administrative support to the project teams in clinical operations
- Supports a number of clinical programs and participates on a number of project teams
- Serves as a member of the Project Team with the goal to contribute towards efficient management of trials
- Manages inventory for clinical trials supplies (consisting of CRFs, study drug where applicable, and other supplies), including the tracking and shipment of material
- Assists the project team with preparation and shipment of Operating Manuals
- Develops and maintains the study specific investigator database for use with correspondence and mail merges
- Updates and maintains study tracking including a master team contact list, in accordance with the demands of the study
- Prepares and distributes initial site start up packages and liaises with the sites to obtain required regulatory documents
- Facilitates communication with the sponsor by shipping required documents and packages to sponsors per project requirements
- Assists team leaders in the production of various study reports and updates
- Serves as an office-based point of contact for all sites during the course of the study as well as provides phone coverage for travelling team members
- Prepares investigator budget payments and distributes to investigative sites
- Serves as administrator of the Trial Master File with direction from Project
- Management, including the preparation, maintenance, and archiving of the
- TMF
- Facilitates project meetings with respect to the preparation and distribution of materials and final meeting minutes, as well as the coordination of participants
- Leanna Reddick
- Form GE-001-E v01 Confidential Page 2 of 3
- CV
SCIENTIST
Immunoreagents
Raleigh, USA
06.2020 - 08.2021
- Identifies and processes Serious Adverse Events according to the procedures defined by the study team
- Assists with study start-up of clinical trials, including feasibility, investigator recruitment, collection of regulatory documents and general site management support
- Develops and maintains good working relationship with investigators and study staff, serving as an ambassador to promote Precision’s high quality and ethical image
- Assists with corporate administration activities according to need and availability
- Performs other duties as assigned by management
- Manufacture antibody conjugates for medical research assays
- Operate the AKTA Process for large scale manufacturing products
- Assist in process improvement and collaboration
- Operated and maintained the large- and small-scale centrifuge
- Process improvement and revision of MPBR’s
LABORATORY ASSISTANT
Immunoreagents
Raleigh, USA
05.2018 - 06.2020
- Manufactured quality antibodies for medical research
- Assembled and operated PALL TFF systems for UFDF at small and large scale
- Ensured that all laboratory equipment remained clean, cared for and in compliance with safety guidelines
- Follow SOP's, MPBR's, GCMP, GCLP and GCDP
- Operated and maintained the large- and small-scale centrifuge
Education
Bachelor of Science - Clinical Research
University of North Carolina Wilmington
Wilmington NC05.2022
A.S - undefined
Richmond Community College
2014
Biotechnology Capstone Certificate - Biotechnology Capstone
Wake Technical Community College
2017
Good Documentation Practices Certificate -
Wake Technical Community College
Good Manufacturing Practices Certificate - undefined
Wake Technical Community College
Skills
- Medical Terminology
- Creative Thinking
- Compassionate Care
- Cold Calling
- Clinical Observations
- System Deployment
- OSHA Regulations
- Problem Resolution
- Providing Feedback
- HIPAA Guidelines
- Medical Coding
- Lab Reports
- Job Assignments
- Document Workflow
- Operational Requirements
- Performance Metric
- Patient Profiles
- Medical Records Requests
- Patient Medical Histories
- Patient Information
- Customer Needs Assessments
- Administrative Support
- Trend Monitoring
- Operational Processes
- Recording Medical Histories
- Data Entry
- Patient Tracking Software
- Product Specifications
- Microsoft Excel
- Annual Evaluations
- Electronic Medical Records Management
- Efficiency Improvement
- Observational Skills
- Study Protocols
- Protocol Design
- Critical Thinking
- Clinical Documentation
- Clinical Trials and Research
- Complex Problem-Solving
- Time Management
- Active Listening
- Research and Data Management
- Applied Statistics
- Data Operations
- Microsoft Word
- Health Literacy
- Clinical Data Collection
- Statistical Analytics
- Microsoft PowerPoint
- Statistical Modeling
- Blood Pressure Measurement
- Data Collections
- Monitoring Data Quality
- Preparing Templates
- Microsoft Access
- Equipment Maintenance
- Drug Storage Procedures
- Data Management
- Medical Records Management
- OSHA Guidelines
Timeline
CLINICAL SUPPORT SPECIALIST I
08.2021 - Current
SCIENTIST
Immunoreagents
06.2020 - 08.2021
LABORATORY ASSISTANT
Immunoreagents
05.2018 - 06.2020
Bachelor of Science - Clinical Research
University of North Carolina Wilmington
A.S - undefined
Richmond Community College
Biotechnology Capstone Certificate - Biotechnology Capstone
Wake Technical Community College
Good Documentation Practices Certificate -
Wake Technical Community College
Good Manufacturing Practices Certificate - undefined
Wake Technical Community College