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PG Diploma in Clinical Research (PGDCR) consists of Clinical Research, Clinical Data Management, Pharmacovigilance & Clinical Trial Data Analysis Using SAS training for 7.5 months.
The module will give students extensive training specific to clinical research associate job responsibilities following industrial standards. All the requirements of the CRA will be taught, and real-time project or on-the-job training will also be provided.
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This module will provide aspirants with a solid understanding of the main issues in the design and interpretation of clinical trials. The module will outline the fundamental principles of comparative clinical trials in investigating effectiveness, efficacy and safety of treatments; and compare the benefits of clinical trials in comparison to alternative study designs.
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This module will cover issues relating to the on-going monitoring of the data in a study in order that sufficient data are available to answer the trial’s question reliably without recruiting more patients than necessary, or exposing them to unacceptable risks. The module will therefore focus on the ethical context of decisions about whether or not to continue entering Patients into trials.
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Module will enable aspirants to understand issues surrounding the risks and benefits of drug use in humans including the cause, manifestations and consequences of adverse drug effects (ADEs), the manner in which these are detected and monitored, and the related historic and legal frameworks.
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SAS training that is designed to train students in applying SAS programming skills to clinical trials. The SAS Clinical training imparts the knowledge and skills required to ensure that clinical data is maintained as per prescribed standards so as to support strategic analysis.
The eligibility criteria for the Post Graduate Diploma in Clinical Research (PGDCR) program are that the Candidates should have completed their graduation degree in any of the following fields: a) Science (e.g., Biochemistry, Microbiology, Genetics, Biotechnology, Botany, Zoology) b) Medicine (e.g., MBBS, BDS, BPT, BAMS, BHMS, BUMS) c) Pharmacy or Pharmaceutical Sciences(e.g B.Pharm, Pharm.D).
After completing a PG Diploma in Clinical Research, graduates can work in various roles such as Clinical Research Associate, Clinical Data Manager, Biostatistician, Clinical SAS Programmer, Pharmacovigilance Specialist, and many more in pharmaceutical and healthcare companies.
Our 7.5-month program PG diploma in clinical research covers major domains like Clinical Research, Clinical Data Management, Pharmacovigilance, Regulatory Affairs, and Clinical SAS. Students benefit from practical, hands-on training and gain expertise in using EDC software like Clinevo and Saftey Database—a valuable advantage for our students!
The PG Diploma in Clinical Research programme at BCRI includes domains like Clinical Research (CR), Clinical Data Management (CDM), Clinical SAS (SAS), Regulatory Affairs (RA), Pharmacovigilance and Drug Safety (PV), Professional and Career Development (PCD), Practical Training and Internship (PTI).
Certainly! Completing the Post Graduate Diploma in Clinical Research (PGDCR) equips graduates with a robust set of practical skills and competencies that enhance their employability in the clinical research job market. Here are the key areas where PGDCR graduates with BCRI benefits, students learn to handle patient recruitment, data collection, adverse event monitoring, and protocol adherence. Understanding regulatory guidelines is crucial. PGDCR covers topics related to Good Clinical Practice (GCP), ICH guidelines, and local regulations. PGDCR imparts skills in clinical data management, including data entry, validation, and quality control, and learns to use statistical tools for data analysis.
Certainly! In a Post Graduate Diploma in Clinical Research (PGDCR) program, students typically gain hands-on experience through various avenues: like Electronic Data Base Capture (EDC) in clinical data management, Safety Data Base in pharmacovigilance, Case processing, Narrative writing, Statistical Analysis Software (SAS) etc..
Yes, on Successful completion of PG diploma in Clinical Research course, we do have 100% placement Support on successful completion of the course. Each student is entitled to placement assistance. Our placement officer is dedicated to finding a suitable opportunity for each student. We are proud to state within a short duration we have been successful in placing our students in the field of clinical operations as CRCs and process coordinators, as drug safety associates in Pharmacovigilance departments, QA personnel in medical writing departments and as Jr. SAS programmers.
Students who have completed a course in clinical research from any other organization may approach us for internship assistance.
We cannot guarantee that a company will hire you, as it is based on your performance during an interview. However, we do provide 100% placement assistance. till date, we have 100% Placement record.
The duration of the Post Graduate Diploma in Clinical Research (PGDCR) program typically is 7.5 months. However,this may vary slightly depending on the add on. During this period, students gain in-depth knowledge about clinical research methodologies, regulations, and hands on experience. PGDCR a valuable program for those interested in pursuing a career in the clinical research industry.
Trainers with extensive experience and expertise in the field of clinical research contribute significantly to the quality of education. We have trainers with high industry experience and research backgrounds. A well-structured curriculum that covers essential topics in clinical research, including regulatory, data management, and practical skills, is a hallmark of our reputable institution. BCRI organizations often incorporate hands-on training, practical exercises, and internship opportunities to ensure that students gain real-world experience in clinical research settings.
A student with a Postgraduate Diploma in Clinical Research (PGDCR) can explore a variety of job roles within the clinical research industry as Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Manager (CDM), SAS Programmer, Clinical Trial Manager (CTM), Drug Safety Associate (DSA), Regulatory Affairs Specialist, Medical writer, Site Management Organization (SMO) Coordinator etc.
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