CLINICAL RESEARCH PROJECT MANAGEMENT AND TRIAL MONITORING
About Us:
PRIVATE CAREER SCHOOL
(Approved by NJ Dept. of Education and Dept of Labor & Workforce Development)
Qtech-Sol Professional Development Center (QPDC) certificate programs are backed and approved by New Jersey Department of Education (DOE) and the Department of Labor and Workforce Development (DOL). We primarily focus on Clinical Research and Trials, Drug Safety-Pharmacovigilance, SAS Data Analytics, and Reporting, Clinical Research Data Management, Clinical Research project Management and Healthcare Business Analysis.
Details:
Qtech-Sol is looking for aspirant students interested and looking to gain experience as practicum needed for Clinical Science Careers. This Clinical Research Project Management and Trial Monitoring (CRPM) program is offered for first 10 selective students subject to interview performance, GPA and meeting eligibility requirements. This is domain-based unpaid practicum, allowing student to gain the experience needed. The learning is tailored per job title and duties as assigned by industry. Practicum learnings of the job is delivered with mix of presentation, quizzes, short description questions and various job specific exercises, along with solutions. At the end the student is subject to take a final exam for certification and recommendations. The learning gained allows the student to apply for various job titles as listed below. Get hands-on required to perform as Clinical Research Project Manager (CRM) with various Pharmaceuticals, Research Hospitals and Clinical Research Organizations (CROs).
Role of Clinical Research Project Manager (CRM)
Clinical Project Manager – Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. Works with Clinical Research Teams, Plan, direct, or coordinate clinical research projects. May also evaluate and analyze clinical data. The job of a project manager is to plan and oversee all aspects of a project, and to meet the project’s goals on time and within budget. It will require you to organize people, tasks and resources to bring about a successful conclusion.
Post Training Support (PTA)
Upon evaluation of submitted tasks a course completion certificate, recommendations and student performance report is shared. Post Training Assistance program is offered for job readiness and this program includes resume preparation, narratives mock session and referral as Intern.
Program Details
https://qtech-solutions.com/program/clinical-research-project-management-and-trial-monitoring-crpm/
Who is Eligible / Education:
Junior and Senior students pursuing,
Associate degree or Above, with Science Major. Biology, Chemistry, Microbiology, Biochemistry, Biotechnology, Clinical Research, Biomedical Sciences, Medicine, Nursing, Pharmacy, Public Health, Pharmacology, Toxicology, Psychology, Sociology or Healthcare Administration
Career Pathway Prospects:
The following is list of Clinical Research job titles as hired by clients based on highest education and experience.
- Clinical Research Associate-Level I & II
- Clinical Research Associate – Level III
- Clinical Research Specialist
- Clinical Program Manager
- Clinical Trial Manager
- Clinical Study Manager
- Clinical Site / Project Manager
Program Duration:
14 Weeks / 335 Hours (Need to Spend min 2-3 hours/ day)
Schedule:
Program Start Date: 12-30-2020 (mm-dd-yy)
Program End Date: 04-14-2021 (mm-dd-yy)
Note: Apply along with your resume to Qtech-Sol Human Resource Division at qpdc@qtech-solutions.com
Applicant student will be called for interview for discussion and next steps.
Contact:
Program Director
Qtech-Sol Professional Development Center
3 Executive Drive, Suite 320
Somerset, New Jersey USA 08873
Phone: +91 95362 27722 (INDIA)
+1 732.207.4564 (USA)
Email: qpdc@qtech-solutions.com
Web : www.qtech-solutions.com