Clinical Research Coordinator Resume Example Company Name

CLINICAL RESEARCH COORDINATOR

Professional Summary

Responsible LPN with excellent communication skills demonstrated by 20 years of experience in healthcare. Accredited Clinical Research Coordinator with over 10 years of experience in the ares of Oncology, Alzheimer disease and Pain Management

Skill Highlights

Research and Analysis Computerized charting specialist Data QC and Integrity Medical clinical procedures comprehension Critical Thinking Problem resolution ability Extensive Organizational Skills

Professional Experience

05/2016

Clinical Research CoordinatorCompany Name － City, State

Coordinate clinical research trials in the areas of Alzheimer's Disease and Pain Management.
Coordinate multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).
Assesses patients for protocol eligibility and communicates findings to investigator/physician.
Coordinates the implementation of protocol procedures.Operates specialized equipment as needed in assigned area, if applicable.
Assesses and monitors patient responses and adverse reactions; reports same to accountable sources.

05/2016

Oncology AbstractorCompany Name － City, State

Oncology abstrating in the areas of Breast Cancer, Colorectal Cancer, Non-Small Cell Lung Cancer.

Ability to work remotely
Understanding of QC/QA processes
Spotlight Team Member
High level of understanding of Patient Manger workings
Fluent in medical terminolgy
Ensured HIPAA compliance.

09/2015 to 05/2016

Company Name － City, State

Assist in investigator study selection and start-up.
Create clinical project documents according to the protocol, including but not limited to, source documents forms and guidelines, instructions on use, monitoring visit templates and reports.
Identify site issues and coordinate corrective action plans based on needs.
Writing of Standard Operating Procedures based on local and federal requirements with the FDA and ICH guidelines.
Create and utilize Site Payment Database for accurate and timely study specific payments.
Team Leader for implementation of new study database including UAT, data entry and data transfer for interim analysis.
Ensure Adverse Events are reported appropriately, accurately and in a timely manner.
Mange Site Master File contents and work with sites to ensure communication requirements between site and IRB are adhered to.
Review CRF, Informed Consent Documents and query language/narratives.

11/2007 to 09/2015

Clinical Research Coordinator IICompany Name － City, State

Melanoma, Sarcoma and Phase I.
Coordinate multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).
Coordinate clinical trials for Industry sponsored, Cooperative Groups- SWOG, GOG, COG and NRG.
Assesses patients for protocol eligibility and communicates findings to investigator/physician.
Coordinates the implementation of protocol procedures.
Operates specialized equipment as needed in assigned area, if applicable.
Assesses and monitors patient responses and adverse reactions; reports same to accountable sources.
Provides appropriate patient and family education.
Completes a variety of reports, documents and correspondence for regulatory agencies, participating clinical trial sites and for internal purposes.
Collaborates with physicians and other healthcare staff to ensure adherence to FDA and protocol guidelines; identify potential problems and/or inconsistencies and take action as appropriate.
Assist in the preparation and submission of amendments to clinical trials protocols to the IRB.
Provides educational in-services as needed.
Promotes interdepartmental cooperation and coordination for each protocol.
Maintains reasonably regular, punctual attendance consistent with Orlando Health policies, the ADA, FMLA and other federal, state and local standards.
Maintains compliance with all Orlando Health policies and procedures.

03/2006 to 10/2006

Clinical Research CoordinatorCompany Name － City, State

Obtaining and documenting Informed Consent per Good Clinical.
Practice.
Completing CRFs both paper and electronic with accuracy.
Creating source documents for Phase I and Phase II studies.

02/2004 to 11/2007

Dosing NurseCompany Name － City, State

Monitor patient responses to treatment and side effects.
Educate patient regarding side effects and correct treatment schedule.

Education and Training

2017

Western Governor's University － City, State, United States

Lively Technical Center － City, State, United States

Associate of Arts: Liberal ArtsValenica Community College － City, State, USALiberal Arts

Professional Affiliations

Licensed Practical Nurse - Florida - PN5156202 SoCRA - Member ID - 34034 ONS- Member ID - 355996

Interests

Basic Life Support (BLS) Certification 2007 Licensed Practical Nurse in the State of FL, License number PN5156202 to present

Skills

ADA, clinical trials, Critical Thinking, data entry, data transfer, Database, forms, Team Leader, monitors, Organizational Skills, policies, Problem resolution, protocols, Research, supervising

Additional Information

Licenses Basic Life Support (BLS) Certification 2007
Licensed Practical Nurse in the State of FL, License number PN5156202 to present

Resume Overview

School Attended

Western Governor's University
Lively Technical Center
Valenica Community College

Job Titles Held:

Clinical Research Coordinator
Oncology Abstractor
Clinical Research Coordinator II
Dosing Nurse

Degrees

Associate of Arts : Liberal Arts

Clinical Research Coordinator Resume Example

Resume Score: 80%

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