Welcome to Delta Clinical Research

Best Clinical Research Course and Pharmacovigilance training with 100% Job Guarantee from top training institute Pune. Learn skills to work as CRA, CRC, PV, CDM, Medical Coder, Scientific writing, Drug Safety Associate, Medical Data Executive and more.

Delta Clinical Research is known for Best Clinical Research Course and Pharmacovigilance Training Institute in Pune designed and developed by Clinical Research Training experts. We offer an exclusive platform to dream up a successful career and grow in the field of innovation and technology with the help of extensively altered Clinical Research Course by Research scholars. The learning scope covers Clinical Research Training (CTM), Pharmacovigilance Training (PV), Regulatory Affairs, Clinical Data Management, Medical Writing and Medical Coding course in Pune from experienced industry experts.

Career in Clinical Research is the best choice for students of life science stream and enthusiastic towards research. Our Clinical Research training program have been rigorously designed to best suit those seeking to enter the field of clinical research, clinical data management, scientific writing & publications, regulatory, Pharmacovigilance, drug safety. To enroll for of this training course.

PG Diploma in Clinical Research Data Management & Pharmacovigilance

Pharmaceutical industry valued at Rs. 900 billion is transforming and growing at a blistering annual pace at the rate of 12-14 percent in India. India is also coming up as a global outsourcing hub in the arena of drug development and research. In addition, India has started the pharmacovigilance Programme in 2010.

Effective and efficient Pharmacovigilance and Clinical Data Management are critical for successful outcomes in clinical research, drug marketing, and a mandated regulatory requirement as well. All this has led to explosive demand for trained and skilled personnel in this field. This Programme aims to train professionals in pharmacovigilance and clinical data management by imparting knowledge and skillsets related to drug safety and total data quality in all phases of clinical trials including post-marketing surveillance

Required For All Programs
We are ISO 9001: 2015 Certified
Our Clinical Partners
Delta Biospecimens
MedTrial Solution
Osaiway Research

Clinical Research Career Opportunities

Clinical Research Coordinator

Coordinate clinical trials,Ensure compliance and documentation and Manage stakeholder communication

CDM & e-TMF

Oversee clinical data collection, Maintain data integrity, Work with electronic data systems,Manage electronic trial documentation, Ensure regulatory compliance, Facilitate document access

Pharmacovigilance Specialist

Monitor and report drug safety, Analyze adverse events data, Ensure regulatory compliance

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Our Courses

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Post Graduate Diploma in Pharmacovigilance

Pharmacovigilance is the process of identifying and responding to drug safety issues and has grown considerably as a discipline over the past 10 to 15 years. We know that, Medicines and vaccines have transformed the prevention and treatment of diseases. In addition to their benefits, medicinal products may also have side effects, some of which may be undesirable and / or unexpected. Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem.

The pharmacovigilance industry are essentially the same as those of regulatory agencies; that is to protect patients from unnecessary harm by identifying previously unrecognised drug hazards, elucidating pre-disposing factors, refuting false safety signals and quantifying risk in relation to benefit.
Post Graduate Diploma in Pharmacovigilance is blended (Online + Offline) program in pharmacovigilance provides you basic & advance knowledge in pharmacovigilance principles and operations. The program also provides training on pharmacovigilance systems, global safety standards, guidelines and regulations & hands on training related to pharmacovigilance. The training curriculum is fully designed by expert faculty and is appropriate for candidates who wish to enter the pharmacovigilance sector.

  • Eligibility: B.Pharm / M. Pharm / Life science/ Medical graduates and post graduates
  • Duration: 6 Months ( 4 Months Theoretical + 2 Months Practical Internship )
  • Placement: 100% placement assistance
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Post Graduate Diploma in Clinical Data Management

Clinical Data Management (CDM) covers the process of collecting, validating, and preparing the data towards statistical analysis for clinical trials. This starts with setting up a clinical data collection tool(s) or a clinical database based on study protocol to collect and store data. The goal is to gather as much of such data for analysis as possible that adheres to federal, state, and local regulations.

The field of clinical data management (CDM) has come about due to demands from both the pharmaceutical industry and the regulatory authorities. As the drive to “fast-track” the development of pharmaceutical products continues to accelerate, regulatory entities have responded by requiring quality-assurance standards to be met in collecting the data used in the drug evaluation process.
Post Graduate Diploma in Clinical Data Management is a blended (Online + Offline) training course intended to deliver training from knowledge in clinical research, ICH GCP guidelines and advance clinical data management. In this program we aim to provide you an deep knowledge and pleasant learning experience so as to transform you into a competent, proficient and successful professional who is highly employable and equipped to perform in your clinical data management career.

  • Eligibility: Life science/ Medical/ Pharma graduates and post graduates
  • Duration: 6 Months ( 4 Months Theoretical + 2 Months Practical Internship )
  • Placement: 100% placement assistance
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Post Graduate Diploma in Clinical Research

Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical research is different from clinical practice. In clinical practice established treatments are used, while in clinical research evidence is collected to establish a treatment.

The Post Graduate Diploma in Clinical Research has been perfectly structured by expert faculties of JCL themselves and thus comprehensive coverage and understanding of the industry and its functional areas is promised. The Offline & Online live interactive course has its own advantages which are definite to benefit one to all participants. We targets to teach, train and polish aspirants in Clinical Research professionals with clear understanding and complete knowledge of this industry and its working.

  • Eligibility: Life science/ Medical/ Pharma graduates and post graduates
  • Duration: 1 Year ( 6 Month Theory + 6 Month Paid Internship) 6 Month ( 3 Month Theory + 3 Month Internship)
  • Placement: 100% placement assistance