Flying Bird

Finance Analyst

Research Assistant

Vikas Jat is the visionary founder of FLYING Bird, a dynamic company at the forefront of the stock market industry. With a deep passion for finance and a keen understanding of market trends, Vikas has established himself as a leading expert in the field. 

Throughout his career, Vikas has demonstrated a remarkable ability to navigate the complexities of the stock market with precision and insight. His strategic thinking and innovative approach have set him apart, earning him a reputation for excellence among his peers and clients alike.

Driven by a relentless pursuit of excellence, Vikas is committed to empowering individuals and businesses to achieve their financial goals through informed decision-making and strategic investments. His dedication to continuous learning and growth ensures that he stays ahead of the curve in an ever-evolving market landscape.

As a seasoned professional with a proven track record of success, Vikas Jat is a trusted advisor and mentor to many in the industry. His expertise, coupled with his unwavering commitment to client satisfaction, makes him a valuable asset to any organization seeking to thrive in the competitive world of finance.

Connect with Vikas on LinkedIn to stay updated on the latest market insights and trends, and discover how FLYING Bird can help you soar to new heights in your financial journey.

📧 :- Vikasjat9784@gmail.com

Vikas Jat

ICON plc

Clinical Trial Manager

Lifebrain

Responsibilities
To act as diagnostic director, reviewing and approving protocols and SOPs related to diagnostic analyses, with responsibility for implementing the system with appropriate methodologies dedicated to private and public settings i.e., clinical studies, services for companies and institutes. To communicate effectively with clients and makes sure to provide services in a timely manner. To support business development and strategic planning; devices and diagnostic software (LIMS) implementation, Telemedicine, Imaging and eCOA. To lead local teams i.e., biologists, nurses, specialists, and technicians, for specific T.A. and working areas.

Director Diagnostic

SINOVAC BIOTECH LTD.

Responsibilities
To assist reviewing, developing and/or writing processes for clinical trial documents, during the startup phase, with responsibility for defining budget and local cost requests and establishing recruitment plans.
To support risk assessment and management and to assess the level of implementation of risk management activities.

Clinical Trial Manager (phase I, immunity covid-19) 

Università di Roma Tor Vergata

Associate Professor in Clinical Biochemistry and Clinical Molecula Biology (Fascia: II, Sector: 05 / E3) at AOUS Siena University Hospital and Rome University “Tor Vergata” (01/06/2018 - in progress; Rome and Siena, Italy) - Accomplishments: i) teaching at specialization courses in Clinical biochemistry and, at the master Chemical, Biological, Radiological, Nuclear, and high yield Explosives courses.
Author/co-author of more than 50 published papers (PubMed & ResearchGate & Linkedin).

Professor

IQVIA

Responsibilities
To act as the Functional Lead from Clinical Research Services with responsibility for delivery of all clinical aspects of clinical II-III phase studies. To assist in the review, development and/or writing of synopsis, protocol and SOPs-GCP compliance. To oversee and serve as the liaison between the Project Manager and a group of CRAs assigned to a given clinical study, for the delivery of all aspects for the start-up phase, monitoring (i.e., conducting co-monitoring visits as needed), site management and study closure.

Recordati

Responsibilities
To act as the Functional Lead with responsibility for delivery of all clinical aspects of clinical phase II studies. To assist the developing, reviewing, and/or writing protocol process. To participate in monitoring study safety and audit. To oversee and serve as the liaison between the Project Managers and a group of monitors assigned to a given clinical study, for the delivery of all study aspects for monitoring phase, reviewing monitoring reports (i.e., conducting co-monitoring visits as needed).

Clinical Trial Manager 

Esercito Italiano - Italian Army

Responsibilities
To act as the responsible in the monitoring of quality system regulation Designed, according to Military standard (Mil STD) and ISO, leading the evaluation of concept and analysis feasibilities, with responsibility for overseeing the process of testing. To select and coordinate activities of vendors for clinical health technologies (i.e., portable devices and POCT). To review monitoring reports for accuracy and GMP compliance.

Clinical Project Manager, Lieutenant (medical devices) 

Clinical biochemist - Associate Professor in Clinical Biochemistry and Clinical Molecula Biology - Extensively experience in Clinical Research and Biotechnology (15 years)

The major focus of my work has been on Clinical Management from public healthcare system to private pharma/biotech/CRO  settings.
I have an analytical mind and I’m extremely good at problem-solving.
My propositive disposition can lead me to work both in groups and independently with a self-motivation.
Soft skills: 
- Relational skills
strong communication, conflict resolution, interpersonal skills, teamwork 
- Critical thinking
risk management, detail-oriented, problem identification and problem solving
- Proactivity
open mindednes, flexible, ability to work independently, time management

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Vikas Jat

Alessio Cortelazzo

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