Indian Institute of clinical Research & Management (IICRM)offers the following courses looking at current demand in the market.
Indian Institute of clinical research & Management has expanded to provide individuals with additional training options via classroom / distance learning system providing flexible and affordable clinical research training via comprehensive training programs, education modules and interactive Webinars.
On-site services for institutions in need of clinical research training
Clinical Research & Management Courses
PG Diploma Artificial Intelligence in Clinical Research – 1 year
A Postgraduate Diploma (PG Diploma) in Artificial Intelligence (AI) in Clinical Research typically focuses on equipping students with specialized knowledge and skills at the intersection of AI and healthcare.
AI Researcher
Career Opportunities
- AI Researcher
- Clinical Trial AI Coordinator
- Clinical AI Researcher
PG Diploma in Clinical Research & Regulatory Affairs – 1 Year
Our PG Diploma in Clinical Research & Regulatory Affairs typically focuses on providing specialized knowledge and skills related to conducting clinical trials and managing clinical research projects.
Advanced Diploma in Clinical Research & Pharmacovigilance – 6 month
PG Diploma in Clinical Research & Pharmacovigilance typically focuses on providing specialized knowledge and skills related to conducting clinical trials..
PG Diploma Artificial Intelligence in Clinical Research – 1 year
A Postgraduate Diploma (PG Diploma) in Artificial Intelligence (AI) in Clinical Research typically focuses on equipping students with specialized knowledge and skills at the intersection of AI and healthcare.
PG Diploma in Pharmacovigilance
A Postgraduate (PG) Diploma in Pharmacovigilance is a specialized program focused on the science and practice of monitoring and assessing the safety of pharmaceutical products (drugs, vaccines, biologics, etc.) post-approval
M.Sc in Clinical Research 2 year.
A Master of Science (M.Sc) in Clinical Research is typically a two-year graduate-level program that provides specialized knowledge and skills in clinical research methodologies, regulatory affairs, data management, and ethical considerations.
Diploma in Clinical SAS – 6 months
SAS is a powerful tool widely used in the pharmaceutical and biotechnology industries for managing, analysing, and reporting clinical trial data. SAS is a powerful tool widely used in the pharmaceutical and biotechnology industries
Diploma in Medical Coding - 6 months
Medical coding is the process of converting a patient's healthcare information, including medical procedures, diagnoses, necessary medical equipment, and medical services, from the physician's notes.
Job Prospects
Over the year 25,00000 jobs are available in this field
Career In Clinical Research
We offers a comprehensive Education and “Hands-On” Training of the clinical research process, the FDA regulations, GCP (Good Clinical Practice) and the International Conference of Harmonization (ICH) guidelines. Over 15000 people have successfully completed our program
- Clinical Research Associate
- Clinical Research Investigator
- Study Coordinator
- Data Manager
- Biostatistician
- Regulatory Affairs Manager
- Clinical Trials Auditor
- Clinical Projects Manager
- Clinical Research Manager
- Business Development Manager
- Drug Safety Associate
- Medical Writer
Eligibility for Training Program is
- Life Science and Health Care Graduates or Diploma in any Discipline
- B.Sc/M.Sc.,Biotechnology, Microbiology, Genetics, Biochemistry, DMLT, MLT
- M.B.B.S.M.D.,MS.
- B.D.S.,M.D.S.,B.V.SC, M.V.Sc, B.PTh, M.PTh, OPTh, ANM, GNM.
- B.H.M.S., B.A.M.S, B.U.M.S, B.Sc Nursing
- B. Pharma, M.Pharma, D.Pharma
- For SAS : B.C.A, B.com, BCCA,B.E. Any Other Graduates.
- Highly interested participate in the final year can also apply.
Course Description
An interactive program providing distance and classroom training for the clinical research professional, begins with the history of legislation and regulations that govern clinical research and an overview of drug, biologic, and device development. Course participants develop a thorough knowledge base of Good Clinical Practices and International Conference of Harmonization guidelines (E6, E2A), gaining a solid understanding of clinical trial development and management.
This course is designed to provide a brief overview of clinical research, terminology, and acronyms followed by a comprehensive review of FDA GCP and ICH GCP (E6). It also reviews the fundamental elements involved in coordinating a clinical trial from the investigator’s perspective. It includes practical tips and suggestions that can be applied to promote a GCP and HIPAA compliant clinical trial, including preventative measures and problem solving techniques of some of the most common GCP non-compliance issues.
Assistance with job placement & resume preparation.
Placements
IICRM has its proven track record of placement. The placement cell of IICRM proven that no one in the industry can defeat them in placement support.
IICRM is serving as a catalyst between the institute and industry. IICRM’s students are working with the following companies
