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JobWatch
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.
Jobs via Kelly Services
Clinical Lab Assistant
Valencia, CA
Clinical Research Associate
San Diego, CA
Clinical Trial/Study Manager
Work Remotely
Clinical Research Scientist - Medical Devices
West Chester, PA
Senior Clinical Research Associate
Irvine, CA
Associate Director, Clinical Operations
Gaithersburg, MD
Clinical Drug Safety Scientist
King Of Prussia, PA
Clinical Pharmacology Associate Scientist
West Chester, PA
Clinical Supply Coordinator
Jacksonville, FL
Clinical Study Assistant
Jacksonville, FL
Clinical Study Assistant
Irvine, CA
Clinical Trial Manager
Cincinnati, OH
Clinical Research Associate
San Diego, CA
Lead CRA (Ophthalmology)
Bethesda, MD
Senior Clinical Research Coordinator
Garden Grove, CA
Senior Clinical Data Manager - NIH
Rockville, MD
More Jobs
Clinical Research Coordinator
SWRR
Mesquite, TX
Senior Director, Clinical Technology
WCG MedAvante-ProPhase
Hamilton, NJ
Data Processor
WCG IRB
Puyallup, WA
Clinical Research - Operations Specialist
WCG IRB
Cary, NC
Document Processor
WCG IRB
Puyallup, WA
Data Processor
WCG IRB
Cary, NC
Senior Data Operations Manager
WCG Analgesic Solutions
Wayland, MA
Senior Data Operations Manager
WCG Analgesic Solutions
Cary, NC
Project Manager Clinical Research - China
WCG MedAvante-ProPhase
Remote
IRB Medical Board Chairperson
WCG IRB
Santee, CA
Upcoming Webinars
January 26, 2021
Reducing Complexity in Starting Clinical Trials: More Patients, Faster Startup
1:00 p.m. – 2:00 p.m. EST
We will explore how our collaboration:
- Reduces study startup cycle times by harmonizing processes and common documents across studies;
- Automates workflows for the management of contacting sites and collecting site documentation for IRB/EC submissions;
- And more.
January 27, 2021
Medical Device Clinical Trials in China: Latest Regulatory Developments
11:00 a.m. – 12:30 p.m. EST
Webinar Takeaways:
- Different clinical pathways and how to decide which pathway to choose to support the National Medical Products Administration (NMPA) medical device/in vitro diagnostic (IVD) regulatory submission or postmarket surveillance;
- Key areas you need to pay attention to so as to have the right strategy and tactics to shorten clinical trials and approval times;
- Whether your devices qualify for the real-world data/study Hainan program and how to get into the program;
- And more.
Upcoming Events
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14Apr