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JobWatch
June 18, 2018
Twice monthly, CWWeekly provides featured listings of clinical research job openings, upcoming industry conferences and educational programs from JobWatch, CenterWatch's online recruitment website for both clinical research employers and professionals.
For conferences, webinars, training programs and job postings, join the LinkedIn JobWatch group.
Jobs via Kelly Services
Clinical Research Coordinator II
Minneapolis, MN
Clinical Operations Program Leader — Early Phase
Cambridge, MA
Clinical Study Assistant
Santa Ana, CA
Expert Clinical Manager III
East Hanover, NJ
Clinical Research Associate III
South San Francisco, CA
Scientific Reviewer - NIH
Bethesda, MD
Project Manager-II-Drug development
Raritan, NJ
Clinical Study Specialist / Clinical Trial Document Manager
Wilmington, DE
Clinical Trials Advisor - NIH
Rockville, MD
Clinical Research Coordinator
Phoenix, AZ
Clinical Affairs Manager
Redwood City, CA
Clinical Psychologist
Durham, NC
Clinical Operations Lead
Weston, MA
EMR Support Administrator
Portland, OR
More Jobs
Chief Business Development Officer
Alliance of Multispecialty Research
Knoxville, TN
Regulatory Data Specialist
National Institute of Allergy and Infectious Diseases
Bethesda, MD
Senior Clinical Project Manager
Chimerix, Inc.
Durham, NC
Senior Clinical Trials Associate / Project Manager I
Access Biologicals, LLC
Vista, CA
Senior Clinical Research Coordinator
Elligo Health Research
San Antonio, TX
Data Coordinator — Research
Mayo Clinic
Phoenix, AZ
Clinical Trial Assistant
SillaJen Biotherapeutics Inc.
San Francisco, CA
Clinical Research Assistant
East Coast Institute for Research, LLC
Jacksonville, FL
Upcoming Conference
AUGUST 8-10, 2018
FDAnews — ICH E6 GCP Interactive Workshop
Waltham, MA
SEPTEMBER 10-12, 2018
Mastering EU Medical Device Regulation
Philadelphia, PA
Training Programs
JULY 1-31, 2018
Program Phlebotomy Training — Two Day Training
Various locations
Webinars
JUNE 21, 2018
The Real Impact of Common Rule in 2018: Understanding Nuances, Facilitating Compliance & Implementing Best Practices
Fully understand the key changes to the Common Rule and how they dramatically impact IRBs and virtually every entity engaged in clinical research. Changes to Informed Consent and Broad Consent, the Implementation of Limited IRB Review and much more.
JULY 11, 2018
Preparing for the MDSAP Audit Process: A Case Study from the Manufacturer’s Perspective
Consultant Connie Hoy takes you through the changes — what’s the same, what’s different about the audit and inspection process as the new Medical Device Single Audit Program (MSDAP).
