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Clinical Trial Management Associate

Kelly Services


Location:
Foster City, CA
Date:
04/23/2018
2018-04-232018-05-22
Job Code:
US15TPCT_BH1432344
Categories:
  • Healthcare
  • Clinical Operations
  • Monitoring
Kelly Services
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Job Details

Job Title Clinical Trial Management Associate

Jobid US15TPCT_BH1432344

Location: Foster City, CA, 94404, USA

Description Kelly Scientific Resources is the world's most recognized brand in Scientific Staffing with more than 100 locations in the North America, Europe and the Pacific Rim. Our scientists contribute to the research and development of products that are used daily in the home, such as medical devices or pharmaceutical products. We employ more than 700 clinical research professionals and 4,500 scientists on an average workday on a temporary, project and full-time basis in a broad spectrum of industries and disciplines. We currently have an exciting opportunity in the San Francisco area as a Clinical Trials Management Associate - I

**Description:** Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas.


+ Provides administrative assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
+ Monitors fairly routine study sites, performing routine data collection, source data verification, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required.
+ Under supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports.
+ May assist in compilation of investigator brochures under close supervision.
+ May resolve routine monitoring issues.
+ Assists in preparation of safety, interim and final study reports, including resolving data discrepancies.
+ Excellent verbal, written, interpersonal and presentation skills are required.
+ Must be familiar with routine medical/scientific terminology.
+ Must be familiar with Word, PowerPoint, and Excel.
+ Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
+ Must be able to participate in departmental or interdepartmental strategic initiative under general supervision.
+ Must be able to contribute to SOP development.
Minimum 3 years experience in a clinical operations role with a pharmaceutical company or CRO not academia..

Bachelors Experience a Must

12 month contract

Please apply now for immediate consideration!

**Why Kelly** **®** **?**


With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevantprojects. Our connections can lead you to innovative scientific pursuits you’ll be proud to helpadvance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000scientific professionals last year.

You pursued a career in science to fuel your quest for knowledge and your desire to make the worlda better place. Let Kelly fuel your career—connect with us today.

**AboutKelly Services** **®**

As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connectwith us on Facebook , LinkedIn and Twitter .

Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females,Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and iscommitted to employing a diverse workforce. Equal Employment Opportunityis The Law.



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