Track follow-up tasks
In CTMS, you can view the meeting or event's follow-up in a dedicated interface to monitor the progress of tasks assigned during meetings or events. You can view task descriptions, assignees, due dates, and statuses to ensure responsibilities are clear and actions are completed on time, supporting accountability and smooth follow-through.
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Access the study management page in one of the following ways:
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In the CTMS application header, select the DASHBOARD tab and then select the study dashboard of your interest.
Figure 1. Accessing study management from dashboard
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In the CTMS application header, select the STUDY MANAGEMENT tab. Then from the Study Data List table, select the study name of your interest.
Figure 2. Accessing study management from study data list
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From the left pane, select Communication Management > Follow-up Tasks Tracking.
Figure 3. Accessing follow-up tasks
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On the page that opens, locate the needed task, and select its meeting or event ID. Then do any of the following.
Figure 4. Managing follow-up tasks
If required, you can preview the meeting or event details by selecting Preview
option, and on the page that opens,
analyze the meeting or event details as explained in the following table.
Figure 5. Previewing meeting
Element
Details
Business Type*
Represents the meeting or event's category or type.
Add it into the calendar
Represents whether the meeting or event is added to your calendar.
If the toggle is switched on, the scheduled meeting or event also appears in the calendar of the email account linked to your CONFORM profile. For example, if your registered email is a Microsoft account, the meeting will be visible in your Teams calendar.Title / Topic*
Represents the title of the meeting or event to be discussed.
Site Code*
When the Business Type is Site Communication, then this field represents the code of the site related to the meeting or event.
Site Name
Represents the autopopulated name of the site.
PI
Represents the autopopulated name of the site's PI.
Required Attendees/Participants*
Represents the participants who are required to attend the scheduled meeting or event and their associated details like, name, role, phone number, and email.
Add Optional Attendees/Participants
Represents the optional participants of the scheduled meeting or event and their associated details like, name, role, phone number, and email.
Start Time*
Represents the date and time the meeting or event begins.
End Time*
Represents the date and time the meeting or event ends.
Duration*
Represents the total meeting or event duration.
Timezone*
Represents the meeting or event's time zone.
Periodical
Indicates if the meeting recurs periodically.
For example, if the meeting needs to be conducted weekly or monthly, this setting ensures that the meeting is scheduled to occur at those intervals instead of being a one-time event.
Frequency
If it is a recurring meeting or event, that is Yes is selected in the previous field, then this field specifies when the meeting or event is expected to recur:
Indicates that the meeting occurs daily. When selected, the following options appear:
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Everyday: select to specify that the meeting occurs every day.
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Every Weekday: select to specify that the meeting occurs only on the weekdays and not on the weekends, that is Saturday and Sunday.
Indicates that the meeting or event must be performed on a particular day every week. Once selected, it specifies if the particular day is Monday, Tuesday, Wednesday, Thursday, Friday, Saturday, or Sunday.
Indicates that the meeting or event is conducted once per month. If selected, the following options appear:
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Every [a digit] Day of every month: a numeric input field where the user has specified the exact day of the month (such as, "2" for the 2nd day of each month).
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Every First [a weekday] Day of every month: a day of the week indicating that the activity occurs every first Monday, Tuesday, and so on of every month.
Communication Method*
Indicates either Phone or Email as the communication method.
Location*
Represents the meeting or event location.
Agenda
Displays the meeting or event's discussion points or objectives.
Upload Files
Displays any uploaded and attached material or documents to review or discuss in the meeting.
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In the Task List table that appears, the task row is now editable, enter the details as explained in the following table.
Figure 6. Updating follow-up task
Tip
In the following table, mandatory elements are marked with an asterisk (*).
Element
Details
Task ID
Represents the system-generated sequential number to uniquely identify each task in the list. It is automatically assigned and not editable by the user.
Task Description*
Enter a short summary of the task that needs to be completed.
Assign to*
Select the Role Category or Assignee option to choose the personnel responsible for the task.
Role Category
If you have chosen Role Category in the previous field, then here select the role (PI, CRC, CRA, and so on) that must complete the task.
Assignee
If you have chosen Assignee in the Assign to field, then here select the personnel who is responsible for completing the task.
Due Date*
Select the deadline by which the task should be completed.
Status*
Select the current progress of the task: Not started, On-going, or Completed.
Save
Select
to update the task.Cancel
Select
to dismiss your changes without saving.
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Once you have previewed the required details and saved your updates, the task is managed.
A person responsible for overseeing and conducting the research study at a specific investigational site or multiple sites, depending on the study's design. The role of a PI is multifaceted and involves various responsibilities, such as study oversight, protocol adherence, participant recruitment and informed consent implementation, regulatory compliance, and so on.
In the eClinical system, the Principal Investigator (PI) role that is assigned to a person who oversees the data entering and signs off subjects—gives authorized confirmation that all the entered data is valid and follows the industry standards. The responsibilities of PI can vary depending on study requirements.
A person responsible for the successful planning, execution, and management of clinical trials. The CRC’s scope of work might include study preparation, site setup, patient recruitment, regulatory compliance control, data collection, and more.
In the eClinical system, the Clinical Research Coordinator (CRC) user role is granted to a person who works on a site with subjects and is responsible for entering data to EDC, ensuring the data is entered correctly according to all requirements, and answering queries from data managers on any questionable data pieces.
A person responsible for overseeing and monitoring a clinical trial to ensure it is conducted in compliance with regulatory standards and protocols. The CRA’s scope of work might include protocol review, site selection and initiation, monitoring, data entry control, and more.
In the eClinical system, the Clinical Research Associate (CRA) user role is assigned to a person who works with the sites, and in EDC, mainly has to make sure that the entered data is truthful to the source document. CRA checks the source document in a process called source data verification and ensures that everything entered by the clinical research coordinators is valid to avoid any discrepancies caused by human errors.