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Home » JobWatch

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

  • 26Jan

    Reducing Complexity in Starting Clinical Trials – More Patients, Faster Startup

  • 27Jan

    Medical Device Clinical Trials in China: Latest Regulatory Developments

  • 11Feb

    Lab X.0: Addressing Quality and Compliance Challenges in Laboratory Operations in the COVID-19 All-Digital Era

  • 23Mar

    Data Integrity for GCP Professionals: Core Requirements, Expectations and Challenges

  • 26Apr

    MAGI's Clinical Research vConference — Spring 2021

Featured Products

  • Regenerative Medicine – Steps to Accelerate Development : PDF

    Regenerative Medicine: Steps to Accelerate Development

  • Clinical Trial Agreements — A Guide to Key Words and Phrases : PDF

    Clinical Trial Agreements: A Guide to Key Words and Phrases

Featured Stories

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    Trial Complexity, Endpoints Continue to Increase, Stretching Site Resources

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    Return to Focus on Risk Management Postpandemic Could Prove Challenging to Sites

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    2021 Vaccine Industry Will Continue to be Dominated by COVID-19 Trials, Experts Say

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    COVID-19, Oncology, CNS and Infectious Disease Trials Will Dominate in 2021, Survey Predicts

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
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