A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials.
Qtech - Sol Professional Development Center (QPDC) is a Private Vocational School (PVS) approved by New Jersey Department of Education and Department of Labor and Workforce Development.
At Qtech Solutions Inc, our training programs are designed to help you move forward in your chosen career, by helping you learn these vital roles that are in demand with pharmaceutical and healthcare companies across the US. We know that you have a busy life, so each program is designed to help pace yourself on your own time, allowing you to advance your career without the fiscal and physical strain of a traditional classroom setting. Our Pure Internet Program (PIP) or Blended Online Program (BIP) can be managed on your laptop or tablet, allowing you to fit in lessons whenever you have the time. Alternatively, if you prefer the traditional classroom approach, our Blended Classroom Program (BCP).
Our courses are approved by the State of New Jersey Department of Education and Department of Labor and Workforce and are the equivalent of 2 years of practical work experience. Browse through our catalog below and choose the course that's right for you!.
Our Programs are Available in 2 Different Delivery Systems:
When beginning one of our training programs, it's important for you to choose the programs that match your current education and skill level. We offer a wide range of programs designed to engage any age or education level and help see how you're best suited to.
Our programs include:Overcome the hurdles in getting your first job with our training practicums. Designed like an internship, you can shadow our experts to learn more about the positions you will be moving into and gain valuable networking connections. We are ready to help build the foundation for the rest of your career.
A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials.
A Clinical Research Associate in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials.
A Clinical Research Project / Study Manager (CRM) is responsible for the monitoring, data collection and analysis, and reporting of clinical trials performed and be in compliance with Ethical practices, ICH,
A Drug Safety / Pharmacovigilance Associate (DSA / PVA), known also in the industry as a Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis,
A Drug Safety Associate (DSA) is responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.
A Drug Safety Data Management roles towards project Management and report submissions (DSA) is responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety
A Drug Safety-Pharmacovigilance
Data and Safety Monitoring and report submissions to Authorities.Responsible for the monitoring,data collection and analysis,and reporting of drug safety information for compliance with drug safety regulations per international markets.
A Clinical Research Project / Study Manager(CRM) is responsible for the monitoring, data collection and analysis, and reporting of clinical trials performed and follow Ethical practices, ICH, GCP, and Clinical Safety guidelines per international markets.
A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.
The Clinical Trial Data Analysis and Reporting (CDAR) provides intensive learning on how SAS is used in clinical and pharmaceutical industries. In particular, how codes, analysis and reports are generated using SAS.
A Clinical Research Assistant is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support administrative support, assisting with routine tests and procedures and collecting both data and samples.
The process of drug development is generally divided into two stages: (1) new lead discovery (preclinical research), and (2) new product development (clinical development). Drug Safety - Pharmacovigilance Assistant can work in Pharmaceuticals, Medical Device, Hospitals,
A Healthcare Business Analyst is a professional employed by a Healthcare and pharmaceutical organization, who keep track of the reforms ,
The purpose of analytics in a healthcare organization is to create insights that help achieve strategic goals such as improving clinical quality,
SAS program is the industry-standard statistical tool. QPDC offers Basic SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various industries.
SAS program is the industry-standard statistical tool. QPDC offers Advanced SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various
Qtech Solutions Inc
2250 Boundary Road, Unit # 208