Advanced Diploma in Clinical Research (ADCR)
Dedicated to Excellence in Training
At SRC, we offer an affordable Advanced Diploma program in Clinical Research, designed to provide students with up-to-date knowledge and effective teaching methods. This four-month course equips learners with the necessary skills to excel in clinical research careers.
SRC introduces an innovative approach to learning, allowing students to practically apply the theoretical knowledge and skills they acquire during the Clinical Research courses in real-world industry settings. Embark on a career in a Contract Research Organization (CRO) with confidence!
What We Teach
The Advanced Diploma in Clinical Research program at SRC provides healthcare professionals with a comprehensive learning experience, covering the following essential topics:
Clinical Research
In-depth overview of the clinical research process, including the phases of clinical trials.
Good Clinical Practice (GCP) guidelines, ethical considerations, and regulatory submissions.
Practical knowledge in protocol development and trial management.
Clinical Data Management (CDM)
Techniques for collecting and managing clinical data.
Designing Case Report Forms (CRFs) and validating data for regulatory compliance.
Database creation, quality control, and regulatory standards in clinical research.
Pharmacovigilance
Drug safety monitoring and adverse event reporting.
Risk management and compliance with ICH, FDA, and EMA guidelines.
Formulating risk mitigation strategies and safety data collection.
Regulatory Affairs
Insights into global regulatory requirements for clinical trials and product approvals.
Communicating with regulatory bodies like FDA and EMA.
Ensuring compliance with legal frameworks and international laws in the pharmaceutical industry.
Learning Objectives
Gain a deep understanding of:
Phases 0 through 5 of clinical trials.
Differences between clinical research and medical care.
Key aspects of trial design, data management, and safety monitoring.
Fundamentals of regulatory affairs and Good Clinical Practice (GCP).
FAQs About ADCR
What skills will I gain from the ADCR program?
The program equips you with comprehensive knowledge of clinical trials, regulatory affairs, pharmacovigilance, and clinical data management. You’ll develop skills like protocol writing, trial design, and safety monitoring.
What is the duration of the ADCR program?
The ADCR course is four months long, with daily live sessions, hands-on assignments, and access to class recordings.
Who is eligible?
Graduates and postgraduates in life sciences, pharmacy, or medical sciences like MBBS, BDS, BAMS, and BHMS are eligible to join.
Do you offer placement support?
Yes, SRC offers 100% placement assistance. Past students have secured roles such as Clinical Research Coordinators (CRCs), Drug Safety Associates, and Jr. SAS Programmers.
How are the online ADCR classes conducted?
Classes are conducted via Zoom or Google Meet, with recordings available for lifetime access. Students receive e-notes and assignments.
What sets SRC apart in clinical research training?
SRC’s curriculum combines practical projects with strong industry connections, preparing students for successful careers in clinical research.
How can I enroll in the ADCR program?
Visit SRC’s official website to complete the admissions process or contact the admissions department for assistance.
