Clinical Research

Clinical Management

Your First Step In The World Of Clinical Management

The clinical research industry is one of the largest and fastest-growing industries in the world. This global market funds, performs and disseminates medical research. It operates at the intersection of healthcare and business.

Clinical research is a branch of healthcare science that deals with the study of the safety and effectiveness of new medications, devices, diagnostic products, and treatment regimens intended for human use. An advance PG Diploma in clinical research offers to entail the candidate with knowledge and practically important information about the industry, working modalities, trial methodologies, drug development, post-marketing safety checks, and all other important aspects.

Introduction to Clinical Research

what is Clinical Research?

Clinical Research is a branch of healthcare that deals with the trials of new drug. This research includes trials on healthy human beings and the patients at initial stage. It’s done to decide a line of treatment for deadly diseases. Clinical research is conducted at various research and medical centers. With the help of new drugs professionals can improve the health of a patient

Novel research studies are structured and comprise of a precise study protocol They are carried out in certain conditions. Firstly, they must aim to increase medical knowledge. Secondly, they must be carried out by qualified and trained clinical research professionals. These professionals take all essential measures to protect volunteers who lend themselves to research. Later, they get the approvals of the regulatory bodies and take all the necessary legal and ethical steps. Therefore clinical research field has a lot of growth potential for healthcare professionals.

Scope of Clinical Research

India is the global hub of clinical trials. So, Many MNC's are setting up research centers in India. This is because clinical trials and studies are an integral part of clinical research. Clinical research determines the safety and effectiveness of medicines, devices, and treatment. The safety and effectiveness of medicines and treatments are carried out before their availability in the market. Thus, there is a huge demand for trained clinical research professionals. The demand for professionals is not only in India but worldwide too. For example, Clinical Research provides excellent job opportunities in USA, Europe, Singapore and India. There are more than 2.5 Lakh opportunities worldwide in clinical research. Furthermore, the global clinical trials market size is expected to reach USD 68.9 billion by 2026. It is projected to expand at a CAGR of 5.7% during the forecast period. Therefore, there is a huge scope for clinical Research in the Coming Year.

What is Clinical Research Courses Eligibility & Duration?

The duration of Clinical research courses at Delta Clinical Research Training Institute is 3 months. Candidates should have a minimum of 55% in their graduation. Candidates holding the following degrees are eligible to apply for this course:

  • Any degree in Life Science or Bio Science
  • Any degree in Medicine
  • Any degree in Pharmacy or Pharmaceutical Sciences
  • Any degree in Pharmacy or Pharmaceutical Sciences

Admission Process:

Candidates can easily apply through our website for Clinical Research Courses with 100% Internship assistance. Admission officers will review your application and contact you for further process.

At Delta Clinical Research Training Institute, we have simplified the admission process for our clinical research training program to ensure a seamless experience for aspiring professionals like you. With our user-friendly online application system and dedicated admission officers, we are committed to guiding you every step of the way. Get ready to embark on a rewarding career in clinical research with our comprehensive admission process.

  • Step 1 : Online Application
  • Step 2 : Application Review
  • Step 3 : Contact and Further Procers
  • Step 4 : Enrolment and Confirmation
  • Step 5 : Placement Assistance

Salaries After Clinical Research Courses

A career in clinical research can provide attractive salary prospects for professionals at various levels. Entry-level positions, such as clinical research coordinators or junior CRAS, typically offer starting salaries ranging from Rs 1.8 LPA to Rs 4 LPA. As professionals gain experience and advance in their careers, salaries tend to increase. Mid-level roles, such as senior CRAS or project managers, can earn between Rs 6LPA and Rs 10LPA, while senior management or executive positions, such as director of clinical operations or vice president of clinical research, can command salaries exceeding Rs12LPA or more. However, it is important to note that actual salary figures can vary based on factors such as industry sector, geographic location, and level of education

Career Opportunities In Clinical Research

Clinical research is the most important stream of healthcare science. There is a huge demand for clinical research professionals in India since the early 2000's However, there is a lack of awareness of the clinical research industry. As a result, there is a huge gap in the demand and supply of trained professionals. At the same time, the clinical research industry is booming. Thus, the clinical research industry requires several trained professionals.

Given below are the career opportunities in the Clinical Research Industry:
  1. Clinical Research Associate
  2. Clinical Research Co-Ordinator Clinical Trial Assistant
  3. Medical Coder
  4. Medical writer
  5. PV coordinator PV Associate
  6. Clinical Data Manager
  7. Research Associate
  8. Site Manager-CR
  9. Regulatory Affairs Associate
  10. Clinical Project Manager
  11. Drug Safety Officer

Oncology Clinical trials Training

Management and Monitoring of oncology clinical trials requires specialized training at the level of project manager, Clinical Research Associate, and Clinical Research Coordinator. Oncology Clinical Trials Training (OCTT) is a skill development program with a primary focus on the Management of Oncology Clinical Trials. It captures all the critical aspects of oncology clinical trials al cot great benefit to the personnel who wish to be competent for the domain of oncology clinical trials.

Program Highlights

  • Self-learning study modules/Matchbook course
  • Assignment based evaluation
  • Self-paced schedule (1-6 months)
  • Training Modules
  • Fundamentals of Oncology Clinical Trials
  • Oncology Clinical Trials Monitoring
  • Dummy Clinical Trial Monitoring Kit™MM
  • Unique practical training component through "mock hands-on training material"
  • Placement assistance through regular job postings (via WhatsApp)

Fees Structure

"For detailed information about our fees structure for the advanced PG Diploma in clinical research program, please reach out to our team." Course Duration Fee Structure
1. PG Diploma in Clinical Research/Clinical Trials Management 6 Month Theory + 6 Month Paid Internship with Oncology Study Delegation (Totally 1 year) 85,000-/
2. Certification in Clinical Research, Data Management and Pharmacovigilance. 3 Month Theory + 3 Month Internship (Totally 06 Month) 45,000-/

company goals

The Scope Of Clinical Research Today: Career prospects and job opportunities

Career prospect:

The future of clinical research is bright and limitless. A PG Diploma course in Clinical Research prepares students for careers in the healthcare field. In other words, this course provides the necessary skills and qualifications needed for the professional practice of clinical research. Students pursuing this course can make their career in the following:

  • Healthcare and pharmaceuticals
  • Biomedical engineering
  • Nutrition and public health
  • Analytics, and forensic sciences
  • Bioinformatics, and drug designing
  • Food and beverages

What are the job opportunities after an advance PG Diploma in clinical research?

The clinical Research Industry has grown worldwide at a remarkable pace in recent years. Therefore, once the students complete the course, they get several opportunities. Some such jobs are discussed below:

A clinical trial associate is a health care professional who works on the clinical trial team for a pharmaceutical company. The clinical trial associates perform administrative and clinical research/clinical trials tasks.

The Clinical Research Coordinator is the individual who oversees the research process for a clinical trial. The coordinator works closely with patients and medical staff to ensure timely study participants and all tests. The clinical research procedures and treatments are carried out in accordance with the study's protocol. The clinical research coordinator is responsible for the following tasks:
  • Matching research subjects with clinical trials.
  • Conducting pre-trial interviews and medical examinations of trial subjects.
  • Maintaining patient records, including patient consent forms.
  • Ensuring that all trial procedures are followed.

A senior clinical research associate has experience and knowledge in the field. Therefore, they provide the necessary expertise and guidance in clinical research. The role of the Senior Clinical Research Associate (SCRA) is to lead a team of research associates in conducting clinical trials. The SCRA is responsible for managing the clinical trial process and overseeing daily operations, including the study protocols, clinical trial budgets, and timelines.

The position is both a management and administrative role as they are required to manage the day-to-day operations of the clinical trials team clinical trials and oversee the planning of research.

Also read How to become a Clinical Research Associate?

A medical coder is a person who enters and codes medical billing data into an electronic form for a health care provider. The role of a medical coder is to make sure the medical record is in order and complete. This can require gathering data from other sources, coding information into a format that makes sense, and creating the final file.

A medical writer is a professional who writes health-related texts. Often, they are the person that conveys scientific information to patients and doctors by translating research findings into language accessible to all. Medical writers are responsible for the accuracy and completeness of medical documents, including patient consent forms, medication information sheets, brochures, and more. Medical writers are responsible for creating text, images, and video content that is not only understandable but also compelling.

The role of a clinical trial writer is to design, write and edit the technical content for a clinical trial. This includes formulating study protocols and procedures, such as writing scientific manuscripts and therapies. Clinical trial writers can also help individuals or organizations conduct research studies on the effectiveness of medical treatments and interventions. They are responsible for managing the scientific team and timelines; writing the patient information booklet, consent forms, and other related clinical trial documents.

Features of our advance PG Diploma in clinical research: What do you get?

Well-structured courses at affordable pricess

Examination and certifications

100% internship and 100% placements for all students

Group Discussions, Mock Interviews, and Aptitude Preparations

Provision of modern infrastructures

A provision of lifetime support, which means that the student is guaranteed a life-long course of study. The provision of life support in advance PG Diploma in clinical research course is the requirement by universities to offer students the opportunity to extend their courses

beyond the current academic year. This idea is to ensure that students have the support they need to continue their academic and professional growth during their lifetime.

Topics Covered Under This Diploma Program

The entire course of advance PG Diploma in clinical research covers all the important and necessary modules, some of which are discussed below:

A clinical trial is a research study in which one or more experimental therapies, nutraceuticals, and other types of interventions are tested for safety and effectiveness. In other words, clinical trials can be designed to test pharmaceuticals, medical devices, procedures, diagnostic tests. The duties of a clinical research associate during clinical trial operations typically include planning, organizing, conducting, and analyzing laboratory experiments for study subjects to provide them with the most effective treatment.

Clinical data management is the study of collecting, analyzing, and reporting clinical trial data. This clinical research course can be broken down into three categories: preclinical, clinical trials, and epidemiologic studies. The study of clinical data management is necessary to ensure the safety of participants and adherence to ethical principles.
Also read Clinical Data Management- Everything you need to know about the course

Pharmacovigilance is the process of monitoring drug safety and protecting human health during clinical trials. It involves gathering, analyzing, and disseminating information about adverse events that occur during a trial in surveillance after the marketing authorization has expired. The study of this course is important because it enables the student to identify factors that may have led to the adverse events, and take appropriate corrective actions. Under this study, the pharmacist undertakes the responsibility of ensuring that drugs do not harm patients in clinical trials.

Medical writing is a type of professional communication that focuses on the accurate and persuasive documentation of medical information. It includes the production and dissemination of health-related materials such as papers, books, conferences, and workshops. In addition, medical writing is concerned with what a patient might want to know about their condition or care. PG diploma clinical research covers the following topics:

  • Patient safety and quality of care
  • Patient communication
  • Evidence-based medicine
  • Accurate and unbiased data study

Soft skills are the non-technical skills that complement a person's technical skill set, such as communication and leadership. Clinical research professionals should have a strong understanding of the profession and its norms to be effective in their work. The soft skills for a clinical research professional include creativity, empathy, and as already stated, leadership, and communication.

Methodology, Program Structure, Focus, and Faculty