NW

Natasia

Wilson

Clinical Research

Associate

**** ** ***** **, **** 2036

North Miami Beach, FL, United States,

33160

adzrx2@r.postjobfree.com

305-***-****

Over 10 years in the clinical

healthcare industry supporting

clinical research trials phases I-IV.

Expertise over many therapeutic areas

of focus to support clinical trials and

assuring protocols are followed.

Develop, implement, and coordinate

research and administrative

procedures for the successful

management of clinical

trials.Supporting subject recruitment

efforts for enrollment, engagement,

and retention. Data management

skills and Quality assurance reporting,

and training frequently on new,

complex, protocols. Looking to help a

team optimize workflows to ensure

sponsor-set objectives and timelines

are met efficiently and effectively.

Key Skills

Professional Experience

Education

November 2020 -

June 2022

Masters Degree in Healthcare Administration

South University, West Palm Beach, Fl

August 2015 - May

2020

Bachelors Degree in Health Science Minor : Biology Bethune Cookman University, Daytona Beach, Fl

Certifications

Proficient in Microsoft (Word, Excel,

Outlook and Powerpoint)

Interpreting Physician orders

Strong Communication Skills

Senior Clinical Research Coordinator

Skin and Cancer Associates DBA.Center for Clinical and Cosmetic Research February 2022

- August 2023

- Dermatology phase I-IV Clinical Trials

- Participant Screening; Inclusion/ Exclusion, Informed Consent Form, Protocol Implementation.

- Data Entry, eCRF,Query Resolution

- IRB Correspondence, AE Collection, SAE reporting, QA, CRA collaboration and monitoring overview- sponsor audits

- Drug Accountability

- Monitored patient safety throughout the duration of clinical studies Travel Lead Coordinator

Care Access Research May 2020 - January 2022

- Phase I-IV Clinical Trials

- Participant Screening; Inclusion/ Exclusion, Informed Consent Form, Protocol Implementation.

- Data Entry, eCRF,Query Resolution

- IRB Correspondence, AE Collection, SAE reporting, QA, CRA collaboration and monitoring overview- sponsor audits

- Drug Accountability

Senior Clinical Research Coordinator

Quotient Science January 2014 - March 2020

- Administratively and clinically manage an average of six to eight clinical trials phase I-IV; Adhere to Research SOPs and Good Clinical Practices and the study protocols

- Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials.

Research Certifications

- Research Investigator/ Research Associates for GCP (Good Clinical Practice) - Monitoring Clinical Drug studies - HIPAA - OSHA - CITI Certifications - GCP Course for Clinical Trials involving Investigational DRug Certification - C-SSRS ( The Columbia Lighthouse Project) - Phlebotomy and ECG/EKG

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