Oracle Health Sciences Training Course Catalog

July 2014

Oracle Health Sciences Training Course Catalog

2

Oracle Health Sciences Course List ............................................... 3

Oracle Health Sciences InForm and InForm Direct Training ........ 7

Suggested learning paths for SaaS customers .............................. 7

Suggested learning paths for Enterprise Adoption customers ........ 8

Online options for InForm and InForm Direct end-user training ...... 9

Classroom and Live Virtual Class training .................................... 10

Online Training ............................................................................ 13

Oracle Health Sciences Central Designer Training ..................... 17

Suggested learning paths ............................................................ 17

Classroom training ....................................................................... 18

Live Virtual Class Training ........................................................... 18

Online training .............................................................................. 19

Oracle Health Sciences Central Coding Training ........................ 20

Classroom Training ...................................................................... 20

Online Training ............................................................................ 20

Oracle Health Sciences IRT on Demand Training ....................... 21

Online training .............................................................................. 21

Oracle Health Sciences ClearTrial Training ................................. 22


Online Training ............................................................................ 23

Oracle Health Sciences Clintrial Training .................................... 24

Suggested learning paths ............................................................ 24


Oracle Health Sciences Empirica Signal Training ....................... 28

Classroom & Live Virtual Class Training ...................................... 28

Online Training ............................................................................ 30

Oracle Health Sciences Mobile Clinical Research Associate ..... 31

Online Training ............................................................................ 31

Oracle Health Sciences Oracle User Management Tool.............. 32

Online Training ............................................................................ 32

Oracle Health Sciences Argus ...................................................... 33

Classroom and Live Virtual Class Training ................................... 33

Online Training ............................................................................ 34

3

Oracle Health Sciences Course List

Oracle Health Sciences InForm courses Classroom Online Live Virtual

Class*

InForm New Features Courses InForm for Sponsor Users InForm for Site Users InForm for Sponsor Users (Japanese) InForm for Site Users (Japanese) InForm for Sponsor Users (Investigator Meetings) InForm for Site Users (Investigator Meetings) InForm for Principal Investigators (Investigator Meetings) InForm for Principal Investigators (Signature)

InForm PI Signature (Japanese) InForm for Principal Investigators (Data Entry and Signature)

InForm PI Data Entry and Signature (Japanese) InForm Ad Hoc Reporting for Cognos InForm Train the Trainer InForm―View Only InForm View Only (Japanese) InForm Direct On Demand for Sponsor Users Installing and Setting up InForm Studies and Reporting Releasing an InForm Study InForm User Management InForm Data Viewer / Partial SV Workshop

* A Live Virtual Class allows you to take a course anywhere you have an internet connection and eliminates the need for expensive travel. With the latest in collaborative technology, top instructors, cutting-edge curriculum, and hands-on labs, our Live Virtual Classes offer an exciting combination of traditional content and interactive learning.

4

Oracle Health Sciences Central Designer courses Classroom Online Live Virtual

Class

Using Central Designer Central Designer Rules Workshop Central Designer Administrator Central Designer Train the Trainer

Oracle Health Sciences Central Coding courses Classroom Online

Using Central Coding Managing Central Coding

Oracle Health Sciences IRT On Demand courses Classroom Online

IRT On Demand for Depot Users/Drug Destruction Facilities

IRT On Demand for Drug Supply Managers IRT On Demand for Site Users IRT On Demand for Study Teams

Oracle Health Sciences Clintrial courses Classroom Online

Using Clintrial Enter, Manage, and Retrieve Clintrial Design Clintrial Admin Writing Rules and Derivations in Clintrial Design Using PL/SQL in the Clintrial Environment Using and Setting Up Clintrial Resolve Using Clintrial Lab Loader Using Clintrial Classify Understanding Concepts in Clintrial MultiSite

5

Oracle Health Sciences ClearTrial courses Classroom Online

ClearTrial Plan and Source End User ClearTrial Track for End Users ClearTrial Role-based Plan ClearTrial End User Train-the-Trainer

Oracle Health Sciences Empirica Signal courses Classroom Online

Empirica Signal Jumpstart Empirica Signal Data Mining Results Empirica Signal Data Mining Runs Empirica Signal Reporting Empirica Signal Signal Management Empirica Signal Topics

Oracle Health Sciences Mobile Clinical Research Associate

Classroom Online

Mobile Clinical Research Associate End User Mobile Clinical Research Associate Setting up Alerts Admin

Mobile Clinical Research Associate Setting up Trip Reports Admin

Oracle Health Sciences Oracle User Management Tool

Classroom Online

Oracle User Management Tool for InForm Site and User Management

6

Oracle Health Sciences Argus Classroom Online Live Virtual Class

Argus Standard Edition Implementation Fundamentals

Argus Standard Edition Processing Safety Cases

Argus Standard Edition Jumpstart Oracle Argus Insight Data Mart

7

Oracle Health Sciences InForm and InForm Direct Training

Suggested learning paths for SaaS customers

Classroom course sequence CRC PI Sponsor Users Format Duration *

InForm for Sponsor Users** Classroom, Live Virtual

Class 1 day

Investigator Meetings InForm for Site Users InForm for Sponsor Users InForm for Principal Investigators

Classroom

1 day total

½ day ½ day 1 hour

InForm Ad Hoc Reporting (Not applicable for InForm Direct users)

Classroom, Live Virtual

Class 1 day

InForm Train the Trainer Classroom 3 days

InForm Data Viewer / Partial SV Workshop


Class 1/2 day

Releasing an InForm Study Classroom, Live Virtual

1/2 day

OR - Online course options

InForm for Site Users Online 2 hours

InForm for Sponsor Users Online 3 hours

InForm for Principal Investigators

(Signature) *** Online 1 hour

InForm for Principal Investigators

(Data Entry and Signature) *** Online 1 hour

InForm―View Only Online 1 hour

InForm User Management Online 2 hours

* Online training is self-paced, so durations given are approximate. ** You may substitute the appropriate online course. *** Principal Investigators should choose the Classroom or online course most closely associated with their responsibilities. .

8

Suggested learning paths for Enterprise Adoption customers

Course sequence Sponsor

Users Study

Designers IT Admins Format Duration

InForm for Sponsor Users Classroom,Live Virtual

Class, Online

½ day 1 day

(Online 2 hours)

InForm Ad Hoc Reporting (Not applicable for InForm Direct users)


Class

1 day 1 days

InForm Train the Trainer Classroom 3 days

Using Central Designer Classroom 2 days

Central Designer Rules Workshop Classroom 2 days

Central Designer Administraor Online 1 hour

Installing and Setting up InForm Studies and Reporting

Classroom 2 days

Releasing an InForm Study Classroom Live Virtual

Class 1/2 day


Suggested learning paths for InForm adoption in APAC

Course Sequence Format Duration

InForm Direct for Sponsor Users

Classroom, Live Virtual Class,

and Online 1 day

Using Central Designer Classroom 2 Days

Central Designer Rules Workshop Classroom 2 Days

Releasing an InForm Study Classroom ½ day

Central Designer Administrator Online 1 hour

InForm Ad Hoc Reporting* Classroom, Live Virtual Class

1 day


* Not required for InForm Direct adoption

9

Online options for InForm and InForm Direct end-user training

Training for Site Users CRC PI Sponsors Format Duration

InForm for Site Users Online 1 hour

InForm for Principal Investigators (Signature)

Online 1 hour

InForm for Principal Investigators (Data Entry and Signature)

Online 2 hour

Training for Sponsor Users

InForm for Sponsor Users Online 2 hours

InForm―View Only Online 1 hour


10

Classroom and Live Virtual Class training

Oracle Health Sciences InForm for Sponsor Users

OBJECTIVE Use Oracle Health Sciences InForm to perform typical site and sponsor tasks

associated with clinical data in Oracle Health Sciences InForm studies.

AUDIENCE Clinical study professionals who are responsible for entering, validating, and reviewing

clinical data in Oracle Health Sciences InForm studies

LENGTH 1 day classroom, 1 day LVC

ATTENDEES Maximum 16 for Classroom, Maximum 14 for Live Virtual Class

The following three courses are offered together at investigator meetings only:

Oracle Health Sciences InForm for Site Users (Investigator Meeting)

OBJECTIVE Use Oracle Health Sciences InForm to perform typical site tasks associated with

entering clinical data in Oracle Health Sciences InForm studies.

AUDIENCE Clinical study professionals who are responsible for entering and editing clinical data in

Oracle Health Sciences InForm studies

ATTENDEES Maximum 20

Oracle Health Sciences InForm for Sponsor Users (Investigator Meeting)

OBJECTIVE Use Oracle Health Sciences InForm to perform typical sponsor tasks associated with

clinical data in Oracle Health Sciences InForm studies.

AUDIENCE Clinical study professionals who are responsible for validating and reviewing clinical

data in Oracle Health Sciences InForm studies


Oracle Health Sciences InForm for Principal Investigators (Investigator Meeting)

OBJECTIVE Use Oracle Health Sciences InForm to accomplish typical tasks performed by principal

investigators (PIs) while overseeing a clinical study.

AUDIENCE Clinical study professionals who are responsible for reviewing clinical data

ATTENDEES N/A

Note: When courses are booked for training at Investigator Meetings the price will be based on the number of days the trainer(s) attend(s) the meeting. If no schedule is available at the time of order, the cost will be estimated at 1 day per course up to a maximum of 2 days.

11

Oracle Health Sciences InForm Ad Hoc Reporting for Cognos

OBJECTIVE Use Oracle Health Sciences InForm reporting to produce reports on clinical data.

AUDIENCE Clinical study professionals who are responsible for producing study reports

LENGTH 1 day classroom, 1 day LVC


Oracle Health Sciences InForm End User TraintheTrainer

OBJECTIVE Prepare trainers to deliver Oracle Health Sciences InForm Site and Sponsor Training.

AUDIENCE Client trainers

LENGTH 3 days

ATTENDEES Maximum 8 (recommended minimum 4)

Releasing an Oracle Health Sciences InForm Study

OBJECTIVE Prepare an Oracle Health Sciences InForm study for release into a production

environment.

AUDIENCE Database administrators, network administrators, systems engineers and

administrators

LENGTH ½ day


Installing and Setting up Oracle Health Sciences InForm Studies and Reporting

OBJECTIVE Install Oracle Health Sciences InForm and its reporting and analysis module.

AUDIENCE Administrators, system engineers

LENGTH 2 days


12

InForm Data Viewer / Partial SV Workshop

OBJECTIVE Use Oracle Health Sciences InForm to perform typical sponsor tasks associated with

the Data Viewer Tool and Partial Source Verification settings in Oracle Health

Sciences InForm studies.

AUDIENCE Clinical study professionals who are responsible for validating, and reviewing clinical

data in Oracle Health Sciences InForm studies

LENGTH 0.5 days


13

Online Training

Oracle Health Sciences InForm New Features Presentations for Site Users

OBJECTIVE To provide an overview of the new features and functionality in Oracle Health Sciences

InForm for certified site users.

AUDIENCE This presentation is available to site users who are upgrading from a later version of

Oracle Health Sciences InForm and have previously taken a certification course.

LENGTH Varies

Oracle Health Sciences InForm New Features for Sponsor Users

OBJECTIVE To provide an overview of the new features and functionality in Oracle Health Sciences

InForm for certified sponsor users.

AUDIENCE This presentation is available to sponsor users who are upgrading from a later version

of Oracle Health Sciences InForm and have previously taken a certification course.

LENGTH Varies

Oracle Health Sciences InForm for Site Users

OBJECTIVE Use Oracle Health Sciences InForm to accomplish typical site tasks performed while

running a clinical study.

AUDIENCE Clinical study professionals who enter and update data and respond to queries

LENGTH 1 hour

Oracle Health Sciences InForm for Sponsor Users

OBJECTIVE Use Oracle Health Sciences InForm to accomplish typical sponsor tasks performed

while running a clinical study.

AUDIENCE Clinical study professionals who audit and query data and sign data entry forms

LENGTH 2 hours

14

Oracle Health Sciences InForm for Sponsor Users (Japanese)

OBJECTIVE This course certifies Japanese speaking clinical research associates (CRAs) in the use

of the InForm application.

AUDIENCE Japanese speaking Clinical Research Associates and Sponsors

LENGTH 2 hours

Oracle Health Sciences InForm for Site Users (Japanese)

OBJECTIVE This course certifies Japanese speaking clinical research coordinators (CRCs) in the

use of the InForm application.

AUDIENCE Japanese speaking Clinical Research Coordinators

LENGTH 1 hours

Oracle Health Sciences InForm for Principal Investigators (Signature)

OBJECTIVE Use Oracle Health Sciences InForm to accomplish typical tasks performed while

overseeing a clinical study.

AUDIENCE Clinical study investigators who are responsible for signing forms

LENGTH 1 hour

Oracle Health Sciences InForm PI Signature (Japanese)

OBJECTIVE This course certifies Japanese speaking Principal Investigators (PIs) in the use of the

InForm application.

AUDIENCE Japanese speaking Principal Investigators who sign CRFs and case report books

LENGTH 1 hour

15

Oracle Health Sciences InForm for Principal Investigators (Data Entry and Signature)

OBJECTIVE Use Oracle Health Sciences InForm to accomplish typical tasks performed while

overseeing a clinical study.

AUDIENCE Clinical study investigators

LENGTH 2 hours

Oracle Health Sciences InForm for PI Data Entry and Signature (Japanese)

OBJECTIVE This course certifies Japanese speaking Principal Investigators (PIs) in the use of the

InForm application.

AUDIENCE Japanese speaking Principal Investigators who do data entry and sign CRFs and case

report books.

LENGTH 2 hours

Oracle Health Sciences InForm—View Only

OBJECTIVE Use Oracle Health Sciences InForm to view data while working on a clinical study.

AUDIENCE Clinical study professionals who only need to view information

LENGTH 1 hour

Oracle Health Sciences InForm View Only (Japanese)

OBJECTIVE This course certifies Japanese speaking clinical specialists in viewing subject records

using the InForm application.

AUDIENCE Japanese speaking clinical specialists who view subject data

LENGTH 1 hour

Oracle Health Sciences InForm User Management

OBJECTIVE Perform site and user administration through the InForm user interface.

AUDIENCE New and experienced users of InForm GTM or InForm Direct tasked with performing

user administration activities.

LENGTH 2 hours

16

Oracle Health Sciences InForm Direct On Demand - Oracle Health Sciences InForm GTM 5.5

OBJECTIVE Use InForm Direct On Demand to accomplish typical tasks performed while running a

clinical study

AUDIENCE Clinical Research Associates and Sponsors

LENGTH 2 hours

17

Oracle Health Sciences Central Designer Training

Suggested learning paths

Course sequence CDM Designers,

Programmers Admin Format Duration

InForm for Sponsor Users Classroom

Online 1 day

2 hours InForm Ad Hoc Reporting

Classroom LVC

1 day Installing and Setting up InForm Studies and Reporting Classroom 2 days

Using Central Designer Classroom 2 days

Central Designer Rules Workshop Classroom 2 days

Releasing an InForm Study Classroom, LVC 1/2 day

Central Designer Administrator Online 2 hours Central Designer Train the Trainer

Classroom, LVC

2 days

18

Classroom training

Using Oracle Health Sciences Central Designer

OBJECTIVE Use Oracle Health Sciences Central Designer to create, validate, and deploy studies to Oracle Health Sciences InForm.

AUDIENCE All study designers

LENGTH 2 days


Oracle Health Sciences Central Designer Rules Workshop

OBJECTIVE Create data-entry rules for Oracle Health Sciences InForm using Oracle Health Sciences Central Designer.

AUDIENCE Programmers and study designers who are responsible for creating data entry rules for Oracle Health Sciences InForm using Oracle Health Sciences Central Designer.

LENGTH 2 days



Oracle Health Sciences Central Designer Train the Trainer

OBJECTIVE By the end of this course you will be able to deliver two Central Designer training sessions, using the topics provided, that meet the training structure profile.

AUDIENCE Anyone who needs to deliver Central Designer training.

PRE – REQUISITS

Before taking this course you should have successfully completed the InForm Sponsor

course (online or instructor led), Using Central Designer, and Central Designer

Administration (online) courses.

LENGTH AND ATTENDEES

4 days (up to 8 attendees), 5 days (up to 12 attendees), 2 days for Live Virtual Class (up to 4 attendees)

19

Online training

Oracle Health Sciences Central Designer Administrator

OBJECTIVE Perform Oracle Health Sciences Central Designer administration.

AUDIENCE Oracle Health Sciences Central Designer administrators

LENGTH 2 hours

20

Oracle Health Sciences Central Coding Training

Classroom Training

Managing Oracle Health Sciences Central Coding

OBJECTIVE Set up and administer Oracle Health Sciences Central Coding by

Creating and managing roles, work teams, and user accounts

Managing coding dictionaries

Creating and managing synonym lists, stop word lists, autocoding algorithms, coding

definitions, and assignment rules

Working with administrative reports

Managing system configuration options, job queues, and coding requests

AUDIENCE Coding specialists who perform system setup and administration tasks

LENGTH 1 day


Online Training

Using Oracle Health Sciences Central Coding

OBJECTIVE Use Oracle Health Sciences Central Coding to code clinical data using

Synonyms, stop words, and coding algorithms

Assignment rules

Interactive coding requests using the Coding Browser feature

Coding queries

AUDIENCE Coding specialists

LENGTH 1 hour

21

Oracle Health Sciences IRT on Demand Training

Online training

Oracle Health Sciences IRT On Demand for Depot Users/Drug Destruction Facilities

OBJECTIVE Use Oracle Health Sciences IRT On Demand to enter and edit data, record supply

information, create and run reports, and set up and manage supplies.

AUDIENCE Depot users/drug destruction facilities

LENGTH 2 hours

Oracle Health Sciences IRT On Demand for Drug Supply Managers


information, and report damaged or missing supplies.

AUDIENCE Drug supply managers

LENGTH 2 hours

Oracle Health Sciences IRT On Demand for Site Users



AUDIENCE Site users of Oracle Health Sciences IRT On Demand

LENGTH 2 hours

Oracle Health Sciences IRT On Demand for Study Teams



AUDIENCE Clinical research coordinators (site users)

LENGTH 2 hours

22

Oracle Health Sciences ClearTrial Training


ClearTrial Plan and Source End User

OBJECTIVE Use Oracle Health Sciences ClearTrial Plan and Source to input plan assumptions,

budget, and forecast clinical studies

AUDIENCE Clinical study professionals who are responsible for planning, creating study budgets,

assessing resourcing needs, and analyzing multiple study scenarios.

LENGTH 2 days


ClearTrial Track End User

OBJECTIVE Use Oracle Health Sciences ClearTrial Track to prepare a study plan for project and

financial tracking

AUDIENCE Clinical study professionals who are responsible for tracking and assessing on-going

study progress

LENGTH ½ day


ClearTrial Role-based Plan

OBJECTIVE Utilize key features in the Oracle Health Sciences ClearTrial software to input plan

assumptions and forecast clinical studies

AUDIENCE Clinical study professionals who are responsible for planning, creating study budgets,

assessing resourcing needs, and analyzing multiple study scenarios.

PREREQUISITE It is required that at least one user who has completed the full two-day Plan course be

present during this training

LENGTH 1 day


Oracle Health Sciences ClearTrial End User TraintheTrainer

OBJECTIVE Prepare trainers to deliver Oracle Health Sciences ClearTrial Plan and Source

Training.

AUDIENCE Client trainers

LENGTH 3 days

ATTENDEES Maximum 8

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Online Training

Oracle Health Sciences ClearTrial Plan and Source for End Users

OBJECTIVE To recognize and use the key features in Oracle Health Sciences ClearTrial Plan to input a plan, budget, and forecast clinical studies.

AUDIENCE Clinical study professionals who are responsible for planning, creating study

budgets, assessing resourcing needs, and analyzing multiple study scenarios

LENGTH 2 hours

24

Oracle Health Sciences Clintrial Training

Suggested learning paths

Course sequence Data-entry Operators

Data Managers

Designers, Programmers

Admin Format Duration

Using Clintrial Enter, Manage, and Retrieve Classroom 2 days

Clintrial Design Classroom 4 days

Clintrial Admin Classroom 1/2 day

Writing Rules and Derivations in Clintrial Design

Classroom 1 day

Using PL/SQL in the Clintrial Environment Classroom 3 days

Training for extended modules

*

Data Managers

Study Designers

Programmers Coders,

Dictionary Managers

Format Duration

Using and Setting Up Clintrial Resolve Classroom 1 day

Using Clintrial Lab Loader Classroom 1 day

Using Clintrial Classify Classroom 1 day

Understanding Concepts in Clintrial MultiSite

Classroom 2 days

* The need for training on the extended modules is based on your Clintrial configuration.

25

Classroom training

Using Oracle Health Sciences Clintrial Enter, Oracle Health Sciences Clintrial Manage, and Oracle Health Sciences Clintrial Retrieve

OBJECTIVE Use Oracle Health Sciences Clintrial Enter, Oracle Health Sciences Clintrial Manage,

and Oracle Health Sciences Clintrial Retrieve to perform data entry and data

management tasks, and to query the database.

AUDIENCE Clinical data managers, data entry operators, programmers, and study designers

LENGTH 2 days


Using Oracle Health Sciences Clintrial Design

OBJECTIVE Use Oracle Health Sciences Clintrial Design to

Create protocols and codelists

Define the structure of the Oracle Database tables

Create electronic representation of CRFs (study books), including dynamic blocks

and pages

Create flags and notes

Set up coding thesauruses

Transfer protocol accounts and codelists

Manage metadata through revision control and protocol release management

Work with PL/SQL packages

AUDIENCE Study designers, programmers, system administrators, and data managers

LENGTH 4 days


Using and Setting Up Oracle Health Sciences Clintrial Resolve

OBJECTIVE Use Oracle Health Sciences Clintrial Resolve to identify, track, review, resolve and

document discrepancies, and set up protocols.

AUDIENCE Study designers, programmers, data managers

LENGTH 1 day


26

Using Oracle Health Sciences Clintrial Lab Loader

OBJECTIVE Use Oracle Health Sciences Clintrial Lab Loader to

Batch load data into a lab loader protocol

Process the data

Transfer the data into a clinical data protocol

AUDIENCE Data managers, programmers

LENGTH 1 day


Using Oracle Health Sciences Clintrial Classify

OBJECTIVE Use Oracle Health Sciences Clintrial Classify to

Track, review, and find solutions for values that fail automatic coding

Build and test effective coding thesaurus algorithms

Create coding thesaurus protocols

Set up coding targets and coding related items in a clinical data protocol

AUDIENCE Coding experts, dictionary managers

LENGTH 1 day


Using Oracle Health Sciences Clintrial Admin

OBJECTIVE Use Oracle Health Sciences Clintrial Admin to perform administration tasks that

include

Creating user accounts and user groups

Assigning access rights to users and user groups

Setting system parameters and Oracle storage parameters

Monitoring database storage and space utilization

Viewing system administration reports

AUDIENCE System and database administrators

LENGTH ½ day


27

Understanding Concepts in Oracle Health Sciences Clintrial MultiSite

OBJECTIVE Use Oracle Health Sciences Clintrial MultiSite to

Set up sites, distribution, and replication

Configure sites in distribution and replication environments

Perform basic data entry operations in a replicated environment

AUDIENCE Designers, programmers

LENGTH 2 days


Writing Rules and Derivations in Oracle Health Sciences Clintrial Design

OBJECTIVE Create and test rules and derivations for Oracle Health Sciences Clintrial modules

AUDIENCE Designers, programmers, data managers

LENGTH 1 day


Using PL/SQL in the Oracle Health Sciences Clintrial Environment

OBJECTIVE Use PL/SQL to

Create stored functions and procedures

Create packages

Set up data checks

Write value changed procedures

AUDIENCE Clinical data managers, programmers, and study designers

LENGTH 3 days


28

Oracle Health Sciences Empirica Signal Training

Classroom & Live Virtual Class Training

Empirica Signal Jumpstart

OBJECTIVE Provides users with a general overview of data mining and Empirica Signal.

Specifically, it provides users with the skills necessary to navigate in Empirica Signal,

review data mining results, review case details, create and publish a case series, run

reports and save output view graphs and drill down to detail data and create a saved

list. This course also introduces two features in Empirica Signal that require

customer-specific implementation, Topics and Drug Profiles.

AUDIENCE This course is appropriate for new users of Empirica Signal; however, experienced

users may benefit from this training as well.

LENGTH 0.5 days


Empirica Signal Data Mining Results

OBJECTIVE Provides users with a general overview of data mining runs in Empirica Signal. Specifically, it provides users with the skills necessary to explore data mining results with advanced selection criteria options, select data mining runs with specific characteristics, and explore results graphically.

AUDIENCE This course is appropriate for users who need to review data mining results via results tables and graphs within Empirica Signal.

LENGTH 0.5 days


Empirica Signal Data Mining Runs

OBJECTIVE Provides users with an advanced overview of data mining runs in Empirica Signal. Specifically, it provides users with the skills necessary to rerun an existing data mining run, create MGPS data mining runs with subsets, with stratification, with database restrictions, and with custom terms, and create a logistic regression data mining run.

AUDIENCE This course is appropriate for users who need to create data mining runs within Empirica Signal.

LENGTH 0.5 days


29

Empirica Signal Reporting

OBJECTIVE Provides users with a general overview of the reporting capabilities of Empirica Signal. Specifically, it provides users with the skills necessary to run reports, save and publish report output, and create and publish report definitions, including line listings, summary reports and interactive reports.

AUDIENCE This course is appropriate for users who need to create and run reports within Empirica Signal. It is also helpful for users who need to create queries and understand query logic.

LENGTH 0.5 days


Empirica Signal Signal Management

OBJECTIVE Signal management is an optional feature in Empirica Signal that provides ongoing monitoring of safety signals by enabling users to view disproportionality analysis statistics for successive updates of safety data. Empirica Signal Signal Management training provides users with a general overview of the signal management capabilities of Empirica Signal.

AUDIENCE This course is appropriate for users who need to create and manage signals within Empirica Signal, as part of an ongoing drug safety review process.

LENGTH 0.5 days


Empirica Signal Topics

OBJECTIVE Topics is an optional feature in Empirica Signal that can be used to collect information, e.g., related to the investigation of a drug safety matter. A topic can help users, and optionally other members of their work team, manage an issue throughout its life cycle using a defined workflow, capturing relevant information and decisions. Empirica Signal Topics training provides users with a general overview of the topics features, based upon the sample topic workflow configuration. Specifically, it provides users with the skills necessary to add and work with topics, actions, and attachments; set up work teams and user permissions related to topics; and set up a topic workflow configuration.

AUDIENCE This course is appropriate for users who need to create topics and administer topic workflow configurations within Empirica Signal.

LENGTH 0.5 days


30

Online Training

Empirica Signal Jumpstart

OBJECTIVE This self-paced course provides users with a general overview of data mining and

Empirica Signal. Specifically, it provides users with the skills necessary to navigate in

Empirica Signal, review data mining results, review case details, create and publish a

case series, run reports and save output view graphs and drill down to detail data

and create a saved list.

AUDIENCE This course is appropriate for new users of Empirica Signal; however, experienced

users may benefit from this training as well.

LENGTH 3 hours

31

Oracle Health Sciences Mobile Clinical Research Associate

Online Training

Mobile Clinical Research Associate End User

OBJECTIVE Manage site visits and process trip reports using the Oracle Mobile CRA application on

an iPad or iPhone.

AUDIENCE New and experienced users of the Oracle Mobile CRA application.

LENGTH 1 hour

Mobile Clinical Research Associate Setting up Alerts Admin

OBJECTIVE Set up and configure alerts using the Oracle Business Intelligence Enterprise Edition

and using the Mobile CRA Administration web application.

AUDIENCE New and experienced administrators of the Oracle Mobile CRA application.

LENGTH 1 hour

Mobile Clinical Research Associate Setting up Trip Reports Admin

OBJECTIVE Set up and configure the components of trip reports using the Mobile CRA

Administration web application.

AUDIENCE New and experienced administrators of the Oracle Mobile CRA application.

LENGTH 1 hour

32

Oracle Health Sciences Oracle User Management Tool

Online Training

Oracle User Management Tool for InForm Site and User Management

OBJECTIVE Perform InForm site and user management functions in the Oracle User Management

Tool.

AUDIENCE New and experienced users of the Oracle User Management Tool.

LENGTH 2 hours

33

Oracle Health Sciences Argus

Classroom and Live Virtual Class Training

Argus Standard Edition Implementation Fundamentals

OBJECTIVE The goal of the Oracle Argus Implementation Boot Camp is to understand how to

implement and configure the products included in Oracle Argus Standard Edition

(Oracle Argus Safety, Oracle Argus Interchange, Oracle Argus Affiliate, Oracle Argus

Dossier, Oracle Argus Un-blinding), in addition to Oracle Argus Japan.

AUDIENCE Administrator, Application Developers, Architect, Business Analysts, Functional

Implementer, System Administrator, Technical Administrator, and Technical

Consultant

LENGTH 4 days

ATTENDEES Maximum 6

Argus Standard Edition – Processing Safety Cases

Objective By the end of this course, you will be able to navigate the Argus Standard Edition user interface, create cases and process them through a workflow, perform data reviews, code reviews, and medical reviews, and create, manage, and execute system searches.

Audience This course is for new users of Argus Standard Edition.

Length 3 days

attendees Maximum 10 for classroom, 6 for Live Virtual Class

Oracle Argus Insight Data Mart

Objective The goal of the Oracle Argus Insight Data Mart training course is to understand how Argus Safety Case information is processed by the Oracle Argus Insight Data Mart ETL.

Audience Administrator, Application Developers, Architect, Business Analysts, Functional Implementer, System Administrator, Technical Administrator, and Technical Consultant

Length 2 hours

attendees Maximum 10 for classroom, 6 for Live Virtual Class

34

Online Training

Argus Standard Edition Jumpstart

Objective By the end of this course, you will be able to navigate the Argus Standard Edition user interface, create cases and process them through a workflow, perform data reviews, code reviews, and medical reviews, and create, manage, and execute system searches.

Audience This course is for new users of Argus Standard Edition.

Length 4 hours

If you have questions or need additional information on training offerings, please email [email protected].

mailto:[email protected]

35

Oracle Health Sciences Course Catalog

July 2014

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Oracle Health Sciences Training Course Catalog

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