COURSE

Diploma In Clinical Research

𝐎𝐧𝐥𝐢𝐧𝐞

➥Duration – 3 Months

Theoretical Lectures on Zoom Meetings( Saturday & Sunday -2hr)

➥Training Topics – 07

➥Fees –Rs 40,000

➥One Time –Rs 38,000

SPECIAL OFFER

Early Bird (10 Student) 5000 Off

𝐎𝐟𝐟𝐥𝐢𝐧𝐞

➥Duration – 3 months

In–house lecture( Saturday & Sunday -2hr).

➥Training Topics – 07

➥Fees – Rs 40,000

➥One time – Rs 38,000

SPECIAL OFFER

Early Bird (10 Student) 5000 Off

Training Topics

Which Cover By ICRM

ICRM is an academy with a good reputation in the clinical research industry. We offer Full time, Part-time, and e-learning training modules in Clinical Research education.

3 Months

(Monday to Friday)

2 Hours

➥Modules – 11

➥Duration – 3 Months – Theoretical  (Lectures on Zoom Meetings)

➥Fees –Rs 40,000

➥One Time –Rs 38,000

Early Bird

(10 Students)

5000 Off

➥Modules – 11

➥Duration – 2 months – In–house lecture.

➥Internship – 1 Month

➥Fees – Rs 65,000

➥One time – Rs 63,000

Early Bird

(10 Students)

5000 Off

6 Months

(Saturday and Sunday)

3 Hours

➥Modules -11

➥Duration 6 Months – Theoretical   (Lectures on Zoom Meetings)

➥Fees – Rs 50,000

➥One Time – Rs 48,000

Early Bird

(10 Students)

5000 Off

➥Modules – 11

➥Duration – 4 months – In–house lecture.

➥Internship – 2 Month

➥Fees – Rs 75,000

➥One time – Rs 72,000

Early Bird

(10 Students)

5000 Off

COURSE

Advanced Diploma In Clinical Research

𝐎𝐧𝐥𝐢𝐧𝐞

➥Duration 6 Months

Theoretical Lectures on Zoom Meetings( Saturday & Sunday -2hr)

➥Training Topics -10

➥Fees – Rs 75,000

➥One Time – Rs 72,000

SPECIAL OFFER

Early Bird (10 Student) 5000 Off

𝐎𝐟𝐟𝐥𝐢𝐧𝐞

➥Duration – 6 months

In–house lecture( Saturday & Sunday -2hr).

➥Training Topics – 10

➥Internship – 1 Month

➥Fees – Rs 75,000

➥One time – Rs 72,000

SPECIAL OFFER

Early Bird (10 Student) 5000 Off

𝐓𝐫𝐚𝐢𝐧𝐢𝐧𝐠 𝐓𝐨𝐩𝐢𝐜𝐬

Which Cover By ICRM

ICRM is an academy with a good reputation in the clinical research industry. We offer Full time, Part-time, and e-learning training modules in Clinical Research education.

HURRY UP!

THE CLOCK IS TICKING
AND THE SEATS ARE LIMITED

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P E R S O N A L

$19.99

T E A M

$29.99

ULTIMATE

$49.99

LEARNING MODULES

CLINICAL RESEARCH

Clinical research is a scientific study that involves humans.

Individuals volunteer to participate in carefully conducted studies that ultimately uncover improved methods and knowledge on screening, diagnosis, treatment, and prevention of disease.

ETHICS AND GUIDELINES IN CLINICAL RESEARCH

Ethical strategies ensure the integrity of the research results, they also protect the safety of patients who volunteer to participate in the trials.

Ethical parameters help to prevent participants from being exploited or treated unfairly by the research team.

PHARMACOLOGY AND DRUG DEVELOPMENT

The discipline of clinical pharmacology helps healthcare professionals develop a deep understanding of numerous topics that are essential to the drug development process such as biochemistry, drug metabolism, pharmacokinetics (PK), pharmacodynamics (PD), pharmacometrics (modeling and simulation), pharmacogenomics, human toxicology, drug interactions, and more.

Opportunities

  • Clinical Pharmacologist
  • Medical Advisor
  • Medical Coding

MEDICAL WRITING

Medical writing is a profession dedicated to the communication of medical, scientific, and health information, including clinical research reports, consumer (patient) information, and the development of clinical trial documents that are protocol, Informed Consent Documents, subject Diaries, etc.

Opportunities

  • Medical Writer
  • Content Writer
  • Medical Data Reviewer
  • Safety Medical Writer

CLINICAL TRIAL MANAGEMENT

Clinical Trial management focuses on planning and organizing a project and its resources. This includes identifying and managing the lifecycle to be used, applying it to the user-centered design process, formulating the project team, and efficiently guiding the team through all phases until project completion.

Opportunities

  • Clinical Research Investigator
  • Clinical Research Coordinator
  • Clinical Research Associate
  • Clinical Trial Assistance
  • Project Coordinator
  • Project Manager

CLINICAL DATA MANAGEMENT

Clinical data management(CDM) is the process of collecting and managing research data in accordance with regulatory standards to obtain quality information that is complete and error-free.

The goal is to gather as much such data for analysis as possible that adheres to federal, state, and local regulations.

Opportunities

  • Clinical Data Analyst
  • Clinical Data Manager
  • Data Coordinator
  • Clinical Data Entry
  • Clinical Data Reviewer
  • Project Data Manager

BIOSTATICS

It is a field of clinical research that helps in collecting, analyzing, presenting, and interpreting data.

It helps make decisions concerning the drug’s efficacy, interaction, and line of treatment.

Opportunities

  • Clinical Database Programmer
  • Biostatistician

QUALITY ASSURANCE

Quality Assurance ensures that clinical trials are performed to meet the requirements of Good Clinical Practice, (GCP). This is an international ethical and scientific quality standard for the design, conduct, recording, and reporting of clinical studies that involve human participants.

Opportunities

  • Quality Assurance Associate
  • Clinical Trial Auditor
  • QA Manager
  • QA Lead

QUALITY CONTROL

Quality control (QC) in clinical trials means the procedures that ensure the protection of human subjects from research risk, the reliability of the data, and thereby assuring internal consistency.

Opportunities

  • Quality Control Specialist
  • Quality Control officer
  • Executive Quality Control

SYSTEMS IN CLINICAL TRIAL

Tools/Applications that manage all of the activities related to the setup, conduction, and closeout of clinical trials, including planning, preparation, tracking, monitoring, compliance, and reporting

Opportunities

  • eTMF Specialist
  • EDC database developer

REGULATORY AFFAIRS

The regulatory affairs (RA) department of a pharmaceutical company is responsible for obtaining approval for new pharmaceutical products and ensuring that approval is maintained for as long as the company wants to keep the product in the market.

Opportunities

  • Regulatory Affairs Associate
  • Regulatory Project Manager
  • Compliance Officer

PHARMACOVIGILANCE

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other medicine/vaccine-related problem.

Opportunities

  • Drug Safety Associate
  • Case Processing Manager
  • Drug Safety Specialist
  • Pharmacovigilance Team Lead
  • Safety Associate Trainee

SOFT SKILL DEVELOPMENT

Soft skills include attributes and personality traits that help employees interact with others and succeed in the workplace.

Opportunities

  • Business Development Manager
3 - Months

ONLINE

OFFLINE

3 - Months

ONLINE

OFFLINE

3 - Months

    𝟑 - 𝐌𝐨𝐧𝐭𝐡𝐬

    ONLINE

    • 🕮 Modules – 11
    • 🕮 Duration - 3 months – Theoretical (Lectures on Zoom meetings)
    • 🕮 Fees – 40,000
    • 🕮 One time – 38,000
    • 🕮 Early Bird (10 students) – 5 thousand off

    OFFLINE

    • 🕮 Modules – 11
    • 🕮 Duration - 2 months – In–house lecture.
    • 🕮 Internship - 1 Month
    • 🕮 Fees – 65,000
    • 🕮 One time – 63,000
    • 🕮 Early Bird (10 students) - 5 thousand off