One Day Online Training in Clinical Project Management

Date: March 17, 2025
Time: 10 AM – 4 PM EST

Clinical trials are highly regulated multi-dimensional projects that require constant interactions between the regulators and the sponsors, investigators, other personnel, and even patients involved in the conduct of a given trial. There are many diverse tasks involved in the conduct of a clinical trial starting from the development of a clinical trial protocol, finding and starting clinical trial sites, filing of an IND or IDE application, approvals from IRBs, numerous documents need to be collected to demonstrate compliance with regulations; managing supplies, collecting data, writing reports, and many other things. Clinical project managers need to understand, implement, and trouble-shoot practically all aspects of the clinical trial under them. Clinical project managers have to build teams and have clear perspective of what may be needed for assuring compliance with FDA requirements of a given clinical trial at all times. This one-of-a-kind program will train you in regulatory affairs, clinical operations, monitoring, patient recruitment and retention, planning, medical writing, safety monitoring and practically all major aspects of running a clinical trial.

Why should you attend:
If you are looking to work in the clinical trial industry as a clinical research associate, a clinical project manager, a regulatory affairs expert, an investigator, a coordinator, a nurse, an ethicist, or any of the myriad roles needed to run a clinical trial, this boot-camp is for you. This is the only course of its kind that covers practically all aspects of conducting a clinical trial from a sponsor, physician investigator, regulators and CRO perspective. Students will be required to work as a team and apply the techniques learned in the classes for developing their respective project plans. This one day training is run by experts working in the clinical trial industry to provide a first-hand overview of the practical aspects of conducting a clinical trial. Practical tips for management of a clinical trial project will be provided using case studies from the presenter’s personal experience. If you are aspiring to be a clinical project manager, are sponsoring a clinical trial, supervise clinical trial operations, or would like to become a clinical site, this training is a must for you.

Areas Covered in the Session:

Good Clinical Practices (GCP)
Setting up the Clinical Trial Team and Clinical Site
Clinical Trial Documentation Practices
Introduction to Project Management for Clinical Trial Professionals
Tools for Project Managers
Monitoring of Clinical Trials
Practical Issues with Clinical Project Management

Speaker: Mukesh Kumar

PhD, RAC | CEO, FDAMap

For more info, fill the box below. We will contact you within 24 hrs.

Workshop Fee

Single Registration

$799

Group Registration (5 Persons)

$2599

Group Registration (10 Persons)

$3999

Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.

Terms & Conditions to register for the Webinar

Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com

Payment

We accept credit card, debit card, and PayPal.

Cancellations & Substitutions:

Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.

On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.

Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.

In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.