Post Graduate Diploma in Clinical Trials Management

Cliniminds
Online

Rs 50,000
+ VAT
You can also call the Study Centre
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Important information

  • Post Graduate Diploma
  • Online
  • Bhopal
  • Duration:
    1 Month
Description

To provide a comprehensive introduction to the clinical research process, conduct & management of clinical trials. Learn the skills, knowledge and competencies of a candidate for the Clinical Research Associate and other key positions. Become more familiar with roles/jobs as part of the study team. Extensive Knowledge & application in different aspect s of Clinical Research

Important information
Venues

Where and when

Starts Location
On request
Bhopal
Cliniminds Bhopal 62, Madhu Chambers, Zone II, MP Nagar, 462011, Madhya Pradesh, India
See map

Frequent Asked Questions

· Requirements

MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B.Pharma, Graduate/Post Graduate Degree in Life Sciences, Pharmacology, Pharmacy, Medical Laboratory, Biochemistry, Microbiology, Biotechnology and all professionals working with Pharmaceutical companies, CROs and hospitals.

Course programme

The program would cover:

- Clinical Research Introduction ,ICH GCP Principles & Terminology

- Healthcare Management Issues

- Introduction to Pharmaceutical Industry & Global Challenges

- Ethical Consideration in Clinical Trials

- Global Clinical Research Environment & Opportunities

- Regulatory Affairs

- Principles of Pharmacology & Drug Discovery & Development

- Roles & Responsibilities of Key Stakeholders

- Preparations & Planning for Clinical Trials

- Essential Documentation in Clinical Research & Regulatory Submissions

- Clinical Trials Project Planning & Management

- Study Start up Process

- Clinical Monitoring Essentials

- Compliance, Auditing & Quality Control in Clinical Research

- Organizational Behavior & Human Resource Management

- Financial Management

- Communication Skills & Personality Development

- Project

- Clinical Data Management, Biostatistics, Analysis & Reporting

- Medical & Scientific Content Writing

- Pharmacovigilance

- Bioavailability and Bioequivalence Studies

- Management of Cancer Clinical Trials

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