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June 4, 2018: Job openings, upcoming industry conferences, webinars, training programs and academic programs

June 4, 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
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Regulatory Data Specialist
National Institute of Allergy and Infectious Diseases
Bethesda, MD

Manager of Clinical Research Operations —Hem-Onc Clinical Trials
Penn State Health – Milton S. Hershey Medical Center
Hershey, PA

Consultant-Trial Capabilities
Eli Lilly and Company
Indianapolis, IN

Clinical Research Specialist
Planned Parenthood of Southern New England
New Haven, CT

Clinical Research Coordinator
Company Confidential
New York, NY

Academic Programs

Boston College
Clinical Research Certificate Program
Chestnut Hill Campus, Newton, MA

Drexel University College of Medicine
Master’s/Certificate Programs in Clinical Research Organization and Management
Online

University of North Carolina at Wilmington
MS Clinical Research and Product Development
Online

Upcoming Conference

JUNE 13-14, 2018
Ensuring The Quality Connection with Your CMO
Philadelphia, PA

August 8-10, 2018
FDAnews – ICH E6 GCP Interactive Workshop
Waltham, MA

Training Programs

JULY 1-31, 2018
Program Phlebotomy Training — Two Day Training
Various locations

Webinars

JUNE 14, 2018
Setting and Measuring Quality Objectives for Medical Devices
Dan O’Leary will walk you through the process and give you compliance tools to make warning letters a thing of the past. Special Bonus Material: Participants receive a checklist to help ensure the system is prepared for your next FDA Inspection, Notified Body audit, or MDSAP audit.

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.