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Home » JobWatch

JobWatch

November 15, 2019

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 Study Associate I
Jacksonville, FL

Rave Clinical Programmer
South San Francisco, CA

Clinical Trial Specialist
Raynham, MA

Sr. Clinical Trial Specialist
Blue Ash, OH

Clinical Data Coordinator II
North Chicago, IL

Clinical Data Analyst
New York, NY

Clinical Data Coordinator
South San Francisco, CA

Clinical Compliance Assistant
Santa Ana, CA

Customer Service Representative
Franklin, TN

CI10 - Utilization Management Rep I
Albany, NY

Laboratory Technician (Molecular)
San Diego, CA

Administrative Assistant
Titusville, NJ

Clinical Laboratory Scientist I
Horsham, PA

Production Technician
Gaithersburg, MD

More Jobs

Senior Regulatory Specialist - Cancer Center (Clinical Trials Office)
University of Illinois Cancer Center
Chicago, IL

Clinical Customer Success Specialist
Castor
Hoboken, NJ

Project Specialist
ACI Clinical
Bala Cynwyd, PA

Financial Data and Analysis Manager
WIRB-Copernicus Group Inc
Princeton, NJ

Director, Human Capital Management
WIRB-Copernicus Group Inc
Hamilton, NJ

Project Manager - Clinical Research
Analgesic Solutions, LLC
Wayland, MA

Clinical Research Analyst
PharmaSeek
Madison, WI

Collection Specialist
Western Inst. Review Board
Puyallup, WA

Upcoming Webinars

NOVEMBER 19, 2019
ICH E8 Developments: Are You Sure You’re Up to Date?
1:30 p.m. - 3:00 p.m. EST

With ICH E8(R1) set to be adopted in June 2020, your planning, design and conduct of clinical trials will look different than they do today. Make sure you’re ready to implement the new guidelines. This webinar clarifies how.

Webinar Takeaways:

  • The purpose of the ICH E8 guideline and its relationship to other ICH
    Efficacy guidelines, including ICH E6(R2) (Good Clinical Practice [GCP]) and ICH E9 (Statistical Principles for Clinical Trials)
  • The impact to current research
    practices that could influence your SOPs, procedures, processes and
    documentation pertaining to ICH guidance
  • And more…

NOVEMBER 26, 2019
Increase Compliance, Reduce Risk with Integrated Digital Solutions: Create a Connected System and Streamline Your Operations
1:30 p.m. - 3:00 p.m. EST

First to market: A coveted spot you aspire to reach in the crowded life sciences arena. You have multiple SOPs in place to improve efficiency and ease of use, in an effort to minimize wasted time and win that sought-after place. But you are far more likely to be first to market when your SOPs and digital solutions are integrated, ensuring nothing falls through the cracks. After all, if you don’t know there’s a problem, you can’t address it.

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

  • Virtual Doctoer

    Simple Changes Can Make Trials More Patient Friendly

  • Drug approval

    Two-Thirds of Trial Subjects for Drug Approvals Are Outside the U.S.

  • VaccinewithNeedle-360x240.png

    Rules of Vaccine Approval May Be Changing, But Statistical Analysis Tools Remain Constant

  • AskTheExperts-360x240.png

    Ask the Experts: Trial Operations Adjustments in a Remote World

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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