Ritu Verma is a qualified professional, who works in Natus Medical Incorporated main office of which is in 1160. as a Head of Clinical Affairs from 2018. Ritu gained professional experience in more than seven positions at different companies. Ritu Verma went to the San Francisco State University and received education from 2012 to 2012. This expert has such professional qualifications as Certification In Medidata Rave Study Design and Build Essentials., Certification In Medrio Study Design and Build Essentials., and Certification In Eclinical Os (Merge) Study Design and Build Essentials.. San Francisco, California is the city, where this person was lastly known to live. This professional's e-mail and phone can be easily accessed through SoftwareOfficial by request.
Name variants:
Ritu Verma
Last updated Jun 14, 2024
Contact Information
Last Update
Jul 4, 2022
Email
ri**@yahoo.com, ri**@cardiokinetix.com
Location
San Francisco, CA
Company
Natus Medical Incorporated
Workplace
Head of Clinical Affairs
Work History
Head of Clinical Affairs
6701 Koll Center Pkwy SUITE 120, Pleasanton, CA 94566
Jan 30, 2018 — May 2019
Advisory Board Member
5201 Great America Pkwy Suite #320, Santa Clara, CA
from Jan 2019
Director; Clinical, Etechnology and Process Optimization
7555 Gateway Blvd, Newark, CA 94560
Jul 2017 — Dec 2017
Director, Clinical Affairs
925 Hamilton Ave, Menlo Park, CA 94025
Providing leadership to multiple direct reports while overseeing the day to day coordination, management & operational aspects of multiple global clinical trials to secure the successful co...
Jan 2015 — Jun 2017
Senior Clinical Consultant
820 west Diamond Ave, Gaithersburg, MD 20878
Jan 2000 — Dec 2012
Head of Global Clinical Affairs
6701 Koll Center Pkwy SUITE 120, Pleasanton, CA 94566
from May 2012
Education
2012 — 2012
2008 — 2008
2000 — 2006
Occupations
Executive
Board Member
Management Team Executive
Operations Manager
Skills
Clinical Data Management
Edc
Project Management
Protocol
Gcp
Clinical Trials
Ctms
Validation
Cro
Data Management
Medidata
21 Cfr Part 11
Good Clinical Practice
Crf Design
Cdisc
Regulatory Submissions
Data Validation
Pharmaceutical Industry
Standard Operating Procedure
Cro Management
Electronic Data Capture
Clinical Trial Management System
Clinical Trial Management
Sop
Analytics
Statistics
Cdash
Sop Development
Rave Safety Gateway
21 Cfr Part 312
Gcdmp
Internal Audit