This
web seminar provides an excellent introduction to clinical research data
management, focusing on processes and their rationale, making it ideal for the
new data manager and other individuals who wish to learn basic clinical data
management functions.
- Identify the roles and responsibilities of the
Clinical Data Management (CDM) Research Team
- Discuss the protocol design and
development process and data management
- Recognize the CDM start-up
activities/documentation
- Discuss case report form design,
data tracking and collection, data entry and capture
- Discuss data review, validation, and
queries
- Recognize the rationale of the
MedDRA dictionary
- Discuss database lock and release
- Examine Adverse Event reporting and
reconciliation
- Apply suggestions for future study
- Sponsor/CRO staff with less than one year of
experience and whose function is to review, correct, enter, or manage data
- Individuals who desire a basic
understanding of the function of clinical data management
Denise
G. Redkar-Brown, MT
Click here for complete trainer
biographies
$735
Includes up to 20
participants at one site. All participants (up to 20) are eligible for
“Certificates of Attendance,” and accreditation, provided that accreditation
requirements are met. For groups larger than 20 or for additional sites, please
call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
Barnett International is accredited by the
Accreditation Council for Pharmacy Education as a provider of continuing
pharmacy education. Participants will
receive 2 hours (0.2 CEUs) of continuing education credit for full
participation, including the completion of a pre-test, post-test, and program
evaluation. Barnett International will
issue a receipt of completion for earned CEUs within three weeks of program
completion. ACPE#: 0778-0000-17-038-L01-P.
Released: 2/17.
Hold
this course at your company! For more information, contact Naila Ganatra at +1
215.413.2471.