CLINICAL SCIENCE PROGRAMS
JOB AND SKILL-BASED CERTIFICATION

Qtech Solutions Inc

Introduction

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Introduction

Qtech Solutions Inc., as Private Career School is a Professional Development Center, specializing in providing full-service training solutions towards clinical trial, drug safety and clinical data management adhering to UD-FDA, European EMEA and Health Canada guidelines and compliance. Qtech Solutions Inc., Canada is a Extra provincial company and our wide experience encompasses a range of training solutions in various areas, designed to help manage clinical trial phases, pharmacovigilance operations, study designs and more! Since 2000, we have devoted our attention to the clinical science field, expanding our expertise to provide various training and consulting solutions.

Our Certificate and Career Focus Programs

* Job Focused Certificate programs Preapproved by the Private Training Institution Branch (PTIB), Ministry of Advanced Education, British Columbia , Canada

New Jersey Department of Education
New Jersey Department of Education

Domain Programs (In-Demand - Job Titles)

We Offer Training Solutions focusing 3 Industry Domains

  1. Clinical Research
  2. Drug Safety-Phramacovigilance
  3. Clinical Data Management

The Program

We provide easy-to-understand training, focusing on tasks performed by professionals. Materials are provided through its customized Learning Management System (LMS), which includes a variety of courses, including voice-over presentations, practice quizzes, test quizzes, discussion-based questions, and various work-related exercises and solutions. At the end of the course, students will take a final exam to obtain certification. Qualified candidates will have the opportunity to enroll in our post training assistance (PTA program) to prepare and find a job.

Program Models

Qtech Offers below program models. Student can opt to the best model based on their education background, prior expereince and need.

  1. Job Based Practicum Package
  2. Certificate Program
  3. Skill-Based Lessons

Program Delivery Types

We offer our teaching in 2 ways.

  1. SIP - Self-Paced Online Material with Support
  2. SBP - Self-Paced Online Material with Online Classes and Support

Benefits of our courses

  1. Knowledge required for upgrading.
  2. Better resume positions for promising jobs.
  3. Low investment and high learning.
  4. Learn from anywhere, anytime.
  5. Courses based on positions rather than concepts.

Post Training Support (PTA)

After training, we support our certified students in.

  1. Resume preparation
  2. Narrative writing.
  3. Interview preparation
  4. Job application Leads

CLINICAL RESEARCH AND PROJECT MANAGEMENT

Are you passionate about clinical research and want to be part of a research team to conduct clinical trials? Want to be a clinical research manager in a pharmaceutical , CRO or research hospital. You must have an associate's or bachelor's degree in biology, biochemistry, biotechnology, chemistry, medicine, nursing, public health and other healthcare majors to qualify. At Qtech, we strive to achieve your career goals and make you successful.

What is a clinical study / trial?

Clinical research is medical research that involves people. Clinical trials are research conducted on people to evaluate medical, surgical, or behavioral interventions. Researchers have discovered whether new therapies / new drugs, diets, or medical devices are safe and effective for people. Often, clinical trials are used to find out whether new therapies are more effective and / or have fewer harmful side effects than standard therapies. Clinical trials of drugs are often described in terms of their stage. (I, II, III and IV).

Programs offered

We offer 5 programs, click below to learn more about each program.

CLASS-A (Approved and Reviewed by PTIB BC) - SBP Delivery Model

This program is being reviewed for approval by the Private Training Insitututions Branch (PTIB) of the Ministry of Advanced Education, Skills & Training, Canada.

Clinical Trial Project Management & Monitoring (CRPM) - Package

US-DOE Programs (Approval of PTIB, BC Not required) - SIP Delivery Model

Below programs does not require approval by the Private Training Institutions Branch (PTIB) of the Ministry of Advanced Education, Skills & Training., based on the fee and duration of the course. As such, PTIB did not review these program.

Clinical Research Assistant (CTAA) - Entry
Clinical Research Skill-Based-Lessons (CRSB) - Entry
Clinical Research Associate (CRAT) - Certificate
Advanced Clinical Research (CROP) - Advancement

The Role of Clinical Research professional

It is the responsibility of the clinical researcher to ensure that these trials are conducted ethically with good clinical practice and that all team members adhere to strict regulations. They must handle documents and materials carefully and safely. Overall, researchers are responsible for recruiting and screening patients, maintaining patient care in terms of health and progress, and then submitting results to sponsoring organizations upon completion.

New Jersey Department of Education

The Clinical Research Associate (CRA) can be hired directly by the sponsor company of a clinical trial or by a contract research organization (CRO) (also known as a clinical research organization), which conducts clinical trials on behalf of the sponsor company. The Clinical Research Associate (CRA) is also called a clinical trial monitor. They have a broad description of their work, but their main responsibility is to ensure the rights, safety, and well-being of the participants in clinical trials. The Clinical Research Associate (CRA) serves as the primary means of communication between the sponsor and the site. A clinical research Associate / Assistant (CRA) professional sets up, monitors, and closes clinical trial sites assigned to him / her. Depending on the level of experience, CRA is usually hired by employers at CRA I, II and III levels.

Job titles you can apply after training
Clinical Research Associate Clinical Research Coordinator
Clinical Trial Assistant Trial Regulatory Coordinator
Research Assistant Research Associate
Trial Master File (TMF) Assistant Site Management Specialist
Documentation Specialist Clinical Trial Monitor
Clinical Study Manager Clinical Project Manager

DRUG SAFETY-PHARMACOVIGILANCE

Are you passionate about drug monitoring or surveillance and keen about safety of patients, this career pathways will interest you. Do you have a degree in medicine, pharmacy or nursing? Well, this career path and plan is perfect for you. At Qtech, we strive to achieve your career goals and make you successful.

DRUG SAFETY

Drug safety is the main aspect of medical therapy that can play a major role in deciding which drug should be given to a patient. Pharmacovigilance (PV or PhV), also known as drug safety, is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products.

New Jersey Department of Education

Programs offered

We offer 4 programs, click below to learn more about each program.

CLASS-A (Approved and Reviewed by PTIB BC) - SBP Delivery Model

This program is being reviewed for approval by the Private Training Insitututions Branch (PTIB) of the Ministry of Advanced Education, Skills & Training, Canada.

Drug Safety-Pharmacovigilance Data Management (DSPM) - Package

US-DOE Programs (Approval of PTIB, BC Not required) - SIP Delivery Model

Below programs does not require approval by the Private Training Institutions Branch (PTIB) of the Ministry of Advanced Education, Skills & Training., based on the fee and duration of the course. As such, PTIB did not review these program.

Drug Safety Skill-Based-Lessons (DSSB) - Entry
Drug Safety-Pharmacovgilance Associate (DSAT) - Certificate
Advanced Drug Safety (ADPP) - Advancement

The Role of Drug safety professional

Drug safety associate or assistants work in the medical industry to monitor the safety of medicines and to assess and prevent adverse reactions in patients. A pharmacy safety profession (also known as pharmacovigilance) can include working with clinical research organizations conducting trials, biotechnology companies, pharmaceutical companies, or government agencies such as the National Institutes of Health (NIH). Drug safety assistants need excellent research skills, a solid medical or biological science background, and a deep understanding of the Food and Drug Administration (FDA), European Medicines Agency (EMA) guidelines and regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether a particular drug is safe.

Job titles you can apply after training
Drug Safety Associate Drug Safety Assistant
Pharmacovigilance Associate Adverse Event Monitor
Medical Case Evaluator Local Safety Manager (LSM)
Drug Safety Manager Medical Record Extractor
Medical Reviewer Therapeutic Area Lead
Global Drug Safety Specialist Patient Safety Quality Manager

CLINICAL DATA MANAGEMENT AND SAS

Are you passionate about clinical data analysis and reporting, research, database design, data analysis and modeling, and want to be part of a clinical research team to support clinical trials? This career path is best for you. You must have an bachelor's degree in statistics, mathematics, computer science, biotechnology, medicine or healthcare administration to qualify. At Qtech, we strive to achieve your career goals and make you a successful clinical data manager or SAS data analyst.

Clinical Study and Trials

Clinical research is medical research that involves people. Clinical trials are research conducted on people to evaluate medical, surgical, or behavioral interventions. Researchers have discovered whether new therapies / new drugs, diets, or medical devices are safe and effective for people. Often, clinical trials are used to find out whether new therapies are more effective and / or have fewer harmful side effects than standard therapies. Clinical trials of drugs are often described in terms of their stage. (I, II, III and IV)

New Jersey Department of Education

Programs offered

We offer 4 programs, click below to learn more about each program.

US-DOE Programs - (Approval of PTIB, BC Not required) - SIP Delivery Model

Below programs does not require approval by the Private Training Institutions Branch (PTIB) of the Ministry of Advanced Education, Skills & Training., based on the fee and duration of the course. As such, PTIB did not review these program.

Clinical Trial SAS Data Analysis & Reporting (CDAR) - Package

Clinical Research Data Management (CDMT) - Certification
Basic SAS Programming - Base, Sql, Macros (BSAS)
Advanced SAS Programming - Stat and Graphs (SSAS)

Role of Clinical Data Manager

Clinical Data Coordinators handle clinical information like patient records, appointments, studies, and other official documents. Their role is coordinating activities which relate to clinical administrative tasks and recording data for study and validation.

Clinical data managers are responsible for collecting data from a variety of medical research projects, such as clinical and pharmaceutical trials. They work collaboratively to make sure data is collected, managed and reported clearly, accurately and securely.

Role of Clinical SAS Programmer

SAS is widely used in clinical trial data analysis in pharmaceutical, biotech and clinical research companies. SAS programmers play an important role in clinical trial data analysis. In addition to doctors and clinicians who collect clinical trial data, the group conducting data analysis includes statisticians, clinical data managers (CDMs) and SAS programmers. Statisticians provide the ideas and methods of the data analysis, clinical data managers manage the collected data and control the data quality. In between, SAS programmers implement the analysis methods on the collected data and provide the study summary tables, data listing and graphs to the statisticians and for clinicians to write study report.

CDM Job titles qualified after training
Clinical Data Manager Clincial Data Research Specialist
Clinical Data Analyst Case Report Form Designer
Data Quality Manager Clinical Business Analyst
SAS Job titles qualified after training
Clinical SAS Programmer SAS Data Analyst
SAS Data Modeling Biostatistician
Program Manager Clinical Data Scientist

Contact

Qtech Solutions Inc

2250 Boundary Road, Unit # 208
Burnaby, BC - V5M 3Z3
CANADA

Phone: 604.757.7733
Mail: qpdc@qtech-solutions.ca