Career Awareness Programs (CAP)
Qtech-Sol “Career Awareness Programs (CAP)” are comprehensive course that provides opportunities for students to learn more about the relationship between education and career opportunities, thus supporting them in making positive choices that will affect their future. As the skilled labor gap grows, the conversation around educational gaps and skills gaps is growing as well. Career awareness is a crucial and early step is needed for student to develop their career interests. We empower students to become career ready, with exposure to jobs that align with their interests and aptitudes
Our Job Focused Certificate courses provides opportunities for career exploration. It provides exposer to students to new ideas, career paths, and experiences in the working world and offers solution to close the skills gaps. These are the skills that are not always taught within a traditional classroom setting. We provide an opportunity for students to learn about a clinical science occupation or profession that best fits to your education background. Our self-paced interactive and student-driven Career Awareness courses provides access to current information with wide range of career options for beginners and advanced learners. The student will adapt a four step inquire process commonly used in career planning; knowing yourself; exploring opportunities; making decisions and setting goals; and achieving goals and making transitions.
Qtech-Sol Career Awareness Courses
The Students at Qtech-Sol will have the opportunity to participate in the work simulated tasks as exercises focusing the job, which provides them with a better understanding of work, its conditions, salaries, future, career pathways for the job that interest them. For additional information, please follow the links below to learn about the domain and career pathways.
CLINICAL RESEARCH COURSES
CLINICAL RESEARCH ASSOCIATE
CRA Certification
A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support the progress of clinical trials.
ClINICAL TRIALS MANAGEMENT
Training and Internship Program
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.
ADVANCED CLINICAL TRIALS ASSOCIATE
Research and Management
This program is designed by industry experts for students and young professionals. The training provides in-depth knowledge of the roles and responsibilities of the Clinical Research / Clinical Study Manager, including the theoretical aspect of the field and exposure to variety exercises based on industry requirements.
CLINICAL TRIALS PROJECTS
CRA duties and tasks performed
A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support the progress of clinical trials.
Clinical Research Associate
Skill-Based-Lessons
This Lesson based programs is designed by industry experts for students and professionals. 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. It contains 9 set of chapters.
DRUG SAFETY - PHARMACOVIGILANCE COURSES
A Drug Safety / Pharmacovigilance Associate (DSA/ PVA) also know as Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis of existing and new drugs…
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.
ADVANCED DRUG SAFETY ASSOCIATE
Pharmacovigilance
Their primary role of a Drug Safety professional is to identify safety and risk information, evaluate and report with regulatory authorities. The training program provides in depth knowledge of roles and responsibilities of Drug Safety / Pharmacovigilance Specialist including theoretical aspect of the field and exposure to variety exercises based on industry requirements.
A Drug Safety / Pharmacovigilance Associate (DSA/ PVA) also know as Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis of existing and new drugs…
Drug Safety Associate
Skill-Based-Lessons
This Lesson based program is designed by industry experts for students and professionals. 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. It contains 8 set of chapters.
CLINICAL DATA MANAGEMENT COURSES
CLINICAL TRIALS DATA MANAGEMENT
CDM Certification
A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.
CLINICAL SAS PROGRAMMING
Training and Internship Program
The Clinical Trial SAS 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.
CLINICAL SAS FUNCTIONAL PROGRAMMING
Data Analytics and Reporting
The Clinical Trial SAS Functional Programming (CDOT) provides learnings required to apply regulations, governance and procedures for analysis, monitoring and reporting clinical data using SAS Software.
BASIC SAS PROGRAMMING
Base-Sql-Macros
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.
ADVANCED SAS PROGRAMMING
Stat and Graphs
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
CAREER TRANSITION ASSISTANCE PROGRAM
CAREER TRANSITION ASSISTANCE PROGRAM
Qtech-Sol is a Clinical Science Professional Development Center (Since 2000) supporting fresh students and experienced professional looking for career change and looking to get back to workforce. We help students who are looking for career pathways in clinical science domain in and as Drug Safety Associate (DSA), Pharmacovigilance specialist (PVA), Clinical Research Associate (CRA), Clinical Monitor, Clinical Research Coordinator (CRC), Clinical Trial Assistant (CTA), Clinical Trial Project Manager, Clinical Research Data Management (CDM), Clinical SAS Programmer (SAS) and Healthcare business titles.