Anthony

Mattorano

**** ** ** ******

San Diego, CA 92115

619-***-****

adycz5@r.postjobfree.com

CAREER OBJECTIVE

With extensive experience in medical and clinical trials, I am a dedicated team player seeking a position in the clinical research industry. I aim to utilize my training and expertise to coordinate, monitor, and manage all aspects of clinical trials in adherence to ICH-GCP guidelines, FDA regulations, study protocols, and standard operating procedures. My top priority is to ensure that the welfare and rights of clinical trial patients are safeguarded.

Skills

Ability to listen, identify issues or problem areas, and implement innovative solutions.

Vendor procurement interfacing with labs, imaging centers, and outpatient surgery centers.

Contract and budget negotiations with Vendors and suppliers

Proficient knowledge of a wide range of

eCRF, EDC.

Professional, personable, and articulate.

Collect and submit regulatory-/company-required documents.

DATA/SOFTWARE SKILLS

Medidata Insights, Inform, Rave, ClinPlus.

Ariba

Eclipse

TemPo Link

Self-motivated, energetic, and attentive

to the needs and views of others.

In-depth working knowledge of ICH

GCP guidelines and FDA regulations.

Source data/document verification

(SDV).

Reporting of adverse events (AE/SAE)

according to regulations and company

policy.

Proficiency in reviewing protocol

compliance, focusing on inclusion /

exclusion requirements.

(Protocol, Brochures, Consents, 1572,

contracts/agreement letters, etc.).

Financial Edge, QuickBooks, Microsoft Access.

Microsoft Word, Excel, PowerPoint,

Outlook.

Md Care

Experience

December 2022 – Current

Redly, Inc. Realtor DRE 02198328 SDAR MLS 703317

I marketed properties, provided customer service, used technology tools, showcased properties, negotiated deals, prepared contracts, ensured legal compliance, and gave advice on financing and property matters.

February 2021 – August 2021

Outsourcing Manager

BMS/Axelon Services Corporation/Contingent Employee

As an expert in operations and strategic leadership, I provide guidance, support, and training to teams working on outsourced projects. I ensure that teams are aligned with BMS outsourcing strategies and drive outsourcing activities by working closely with operational teams and vendor stakeholders. I assist in selecting and contracting service providers, ensuring compliance with regulatory standards, ethical practices, and BMS policies and procedures. I also prepare teams for internal and external audits/inspections and ensure that all contract deadlines are met. As an escalation point of contact, I address vendor-related issues and communicate effectively with business partners and internal clients regarding contractual matters.

November 2017 – November 2020

Site Manager/Clinical Applications Laboratories, Inc.

San Diego, CA

I have experience managing the daily operations of a Medical Practice, IV Center, and Research department. My responsibilities include recruiting and enrolling patients into pharmaceutical research projects. To ensure the integrity of clinical research, I thoroughly know research protocols and ensure they are strictly followed. I maintain Source and Electronic Case Report Form documentation, review medical records, liaise between doctors and patients, prepare and ship all laboratory samples, and teach patients about disease management and medication compliance. Additionally, I handle IRB submissions, budgets, and contract negotiations.

JUNE 2015 – NOVEMBER 2017

Administrative Consultant / Computer Network Team

San Diego, CA

I create and implement administrative systems and procedures, oversee projects, and conduct Microsoft Outlook training sessions for corporations.

NOVEMBER 2014 – JUNE 2015

Clinical Contracts Coordinator/Clinical Research Administration/ Veterans Medical Research Foundation

San Diego, CA

As part of my assigned tasks, I thoroughly review contracts related to clinical trials and drug studies. My vast experience in negotiation enables me to represent our interests effectively when dealing with external entities. I work closely with the university and legal counsel to ensure that all contract-related matters are handled seamlessly. Depending on the task, I ensure that accounts are established promptly and that billing is handled accurately.

AUGUST 2010 – JUNE 2012

Site Director/MedResearch Center

La Mesa, CA

As a pharmaceutical research project recruiter, my responsibilities entail enrolling patients and guaranteeing the authenticity of clinical research by acquiring a comprehensive understanding of research protocols and ensuring their strict adherence. I also maintain Source and Case Report Form documentation, review medical records, and serve as a link between doctors and patients, charting the course of patient participation in each research study. Additionally, I perform phlebotomy, prepare and ship laboratory samples, and educate patients on disease management and medication compliance. My duties include handling IRB submissions, budgets, and contract negotiations.

DECEMBER. 2002 – July 2010

Site Director/ Pacific Coast Research Center Inc.

Encinitas, CA

I successfully launched the new research practice by expertly recruiting and enrolling patients in pharmaceutical research projects. My primary duty is to guarantee the authenticity of clinical research by thoroughly understanding research protocols and ensuring their strict compliance. I also maintained Source and Case Report Form documentation, scrutinized medical records, acted as a bridge between doctors and patients, and monitored patient participation in every research study. I was also tasked with performing phlebotomy, preparing and dispatching laboratory samples, educating patients on disease management and medication compliance, and overseeing IRB submissions, budgets, and contract negotiations.

DECEMBER 2002 – July 2006

Educator/Maric College of Medical Careers.

San Diego, CA

As an instructor for the Medical Assisting program, my duties include classroom lectures and practical demonstrations. Among the topics I cover are Anatomy and Physiology, Back Office procedures, and Laboratory practices such as urinalysis, injections, phlebotomy, ECG, and taking vitals. I also ensure that students learn proper sterilization techniques for medical equipment used in the office and understand medical asepsis protocols.

FEBRUARY. 2002 – NOVEMBER 2002

Senior Clinical Research Coordinator/Center for Urological Research.

La Mesa, CA

My role involves recruiting and enrolling patients in pharmaceutical research projects. I am responsible for ensuring the integrity of clinical research by acquiring a thorough knowledge of research protocols and ensuring strict adherence to them. This includes maintaining accurate Source and Case Report Form documentation, reviewing medical records, liaising between doctors and patients, mapping patient participation in each study, preparing and shipping laboratory samples, and educating patients on disease management and medication compliance.

APRIL 2001 - FEBRUARY. 2002

Site Director Research Coordinator/Rokay Kamyar MD., INC

La Mesa, CA

As part of my duties, I collaborate with pharmaceutical companies and Clinical Research Organizations during the pre-launch phase. My responsibilities include the completion of financial and regulatory packets, which I submit to the appropriate departments. I ensure that GCP guidelines are followed at the clinical site. Additionally, I support the daily operations of the medical clinic's front and back offices.

DECEMBER 1999 – April 2001

Research Coordinator/Radiant Research

San Diego, CA

My role involves ensuring research protocols are followed, documenting forms, reviewing medical records, coordinating patient participation, managing lab samples, and educating patients on disease management and medication compliance.

Education

Bachelor of Science in Business Administration / University of Phoenix

San Diego, CA

Graduated with a GPA of 3.8, received a degree in Business Administration, concentration in Business Management.

CERTIFICATIONS

Medical Assistant / Maric College of Medical Careers

San Diego, CA

Graduated from a 9-month program with a GPA of 3.9. Completed a 160-hour internship before receiving certification.

Clinical Research Associate/The Clinical Research Training Institute

Houston, TX

Graduated from a 250-hour Accredited CRA program with a 95% GPA. CRA Professional Development Program

250 hrs. CEU

ICH GCP Training

Clinical Site Monitoring (site selection, initiation, monitoring, and closeout).

Adverse Event Reporting

Pharmacology for Clinical Research Professionals

Certified Clinical Research Coordinator / Association of Clinical Research Professionals (ACRP)

San Diego, CA

Certification achieved as of May -2002- Present.

Department of Real Estate / Salesperson License CA State License ID# 02198328

San Diego, CA

Licensed achieved as of November 17, 2022

MEMBERSHIPS

2022 - PRESENT Department of Real Estate (DRE 02198328)

2022 - PRESENT San Diego Association of Realtors (SDAR MLS 703317)

1997 - PRESENT Association of Clinical Research Professionals (ACRP)

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