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Home » JobWatch

JobWatch

December 22, 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 Contracts Associate
Seattle, WA

Statistical Programmer Analyst Associate
South San Francisco, CA

Global Studies Manager II
South San Francisco, CA

Medical Laboratory Technologist/CLS
Menlo Park, CA

Clinical Project Associate
Foster City, CA

Senior Statistical Programmer
Emeryville, CA

Clinical Lab Specialist
St Louis, MO

Perm IP Clin Doc Analyst
Sacramento, CA

Statistician - NIH
Baltimore, MD

Product Support Coordinator
Palm Beach Gardens, FL

Patient Service Coordinator
Franklin, TN

Clinic Scheduler
Minneapolis, MN

Quality Control Associate
Palo Alto, CA

Medical Technologist
Austin, TX

More Jobs

Lab Director - Life Science Lab
Regenesis Biomedical, Inc.
Scottsdale, AZ

Clinical Research Quality Management Specialist
Gateway Institute for Brain Research
Fort Lauderdale, FL

Director, Service Engagement
WIRB-Copernicus Group (WCG)
Hamilton, NJ

Clinical Project Manager
ACI Clinical
Bala Cynwyd, PA

Document Processor
Western Inst. Review Board
Puyallup, WA

Technology Product Technical Writer
WIRB-Copernicus Group (WCG)
Hamilton, NJ

Contracts Manager
WIRB-Copernicus Group (WCG)
Princeton, NJ

Configuration Analyst
ePharmaSolutions
Plymouth Meeting, PA

Webinars

January 14, 2020
Data Integrity: Latest Regulatory Developments and Best Practices
1:30 p.m. – 3:00 p.m. EST

Do you have a good quality system in place to ensure data integrity? The FDA consistently communicates the importance of supporting data integrity. You need to know when you’re required to report significant data integrity issues discovered pre-submission and the advantages of early disclosure to the FDA — even when no early disclosure obligation exists. Join us on Jan. 14 so you’re ready to tackle any challenges that come up and help companies stay in compliance with the FDA.

January 23, 2020
Real World Evidence and Data: A Tufts Study of 30 Pharma Companies
1:30 p.m. – 3:00 p.m. EST

Real world evidence (RWE) is making its way into your world. Based on their knowledge, and using several recent case studies, Dr. Mary Jo Lamberti — associate director of sponsored research at the CSDD — and Francis Kendall — senior director at Cytel — will share valuable information.

February 12, 2020
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

Win that coveted first-to-market spot. When you integrate your digital solutions you’ll streamline operations, improve quality and mitigate risk. First-to-market is just around the corner.

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

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    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

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

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

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