JobWatch

July 2, 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 (CRC 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 Study Specialist/Clinical Trial Document Manager
Wilmington, DE

Clinical Protocol Coordinator/Navigator
Bethesda, MD

More Jobs

Director, Clinical Affairs
Regional Personnel
Washington, DC

Training & Development Manager
Symbio LLC
Port Jefferson, NY

Chief Business Development Officer
Alliance of Multispecialty Research
Knoxville, TN

Sr. Clinical Project Manager
Shire Pharmaceuticals
Cambridge, MA

Sourcing Associate - Clinical Ancillaries
Thermo Fisher Scientific
Allentown, PA

Clinical Project Manager
Integrium, LLC
Phoenix, AZ

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

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

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

Webinars

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).

JULY 17, 2018
Real-World Evidence Evaluating Benefit & Risk: What Device makers Need to Know
NEST is seen as a real opportunity to find “better, faster, cheaper” approaches to evidence-based generation for device evaluation ... and get your new products to market and to patients in less time.

Upcoming Events

Featured Products

Featured Stories

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here