Read the relevant guidelines for clinical research along with information on the roles and responsibilities of the Clinical Research Coordinator (CRC) in a clinical trial.
The demand for this Course Clinical Trials is expected to have reached a market value of $64B by 2020 compared to the current market value of $38.4B. The market is expected to reflect CAGR of 9% between 2015 and 2020. Actually, ClinicalTrial.gov lists more than 200,000 trials worldwide, providing a range of career options in clinical trial operations and related fields.
The Clinical Research Coordinator (CRC) serves as the key contact channel between the sponsor and the researcher site. The CRC therefore plays a crucial role in the smooth and efficient execution of a clinical trial.
The “Certification Training for Clinical Research Director (CTCRC)” course allows learners to gain an in-depth understanding of the primary principles and processes of clinical research, as well as the comprehensive scope of all positions and responsibilities. The Clinical Research Coordinator undertakes to test at the Investigator Site. See the Curriculum for details. This course will allow clinical research applicants and working professionals to succeed in their careers in clinical research operations as Clinical Research Coordinator (CRC) or clinical trial coordinator (CTC).
Module 1: Introduction to Clinical Research
Module 2: Evolution of Ethical Research principals, Regulations and Guidelines
Module 3: Essential Clinical Trial Documents
Module 4: Clinical Study Process
Module 5: Ethics Review Board (ERB)
Module 6: Roles and Responsibilities of Investigator
Module 7: Roles and Responsibilities of Sponsor
Module 8: Roles and Responsibilities of Clinical Trial Monitor
Module 9: Informed Consent Process
Module 10: Serious Adverse Event (SAE)
Module 11: Maintenance of Source Document
Module 12: IND/ NDA/ ANDA/ AADA
Module 13: Clinical Research Coordinator (CRC) – An Introduction
Module 14: 9 Major Roles and Responsibilities of a CRC – Before Initiation of Clinical Trial Study
Module 15: 12 Major Roles and Responsibilities of a CRC – During Clinical Trial Study
Module 16: 2 Major Roles and Responsibilities of a CRC – After Completion/ Termination of Clinical Trial Study Clinical Trials Terminology Assessment through Online Exam
Length: 12 weeks
Timings: Self Paced
Effort: 55 hrs. approx
Skill Level: All
Includes: LifeTime Access
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