Kelly Services Sr. Clinical Trials Associate in Seattle, Washington

Sr. Clinical Trials Associate —Seattle, WA

As a Sr. Clinical Trials Associate, you will be responsible for performing in-house clinical trial administrative duties in support of the Clinical Development team’s objectives assisting with the coordination of activities associated with the start-up, conduct and close-out of clinical trials. We require prior experience or training in clinical research and knowledge with GCP/ICH guidelines as well as a thorough knowledge of the clinical trials process and associated regulations, responsibilities and roles.

Job Duties and Responsibilities:

  • Collaborating with the Clinical Project Team in the clinical development process, you will assist with:

  • Development and editing of study-related materials

  • Planning, coordination and presentation of information at Investigators’ meetings

  • Site management at the direction of other clinical personnel

  • Providing support to the clinical sites and clinical team members during the conduct of clinical trials

  • Management and tracking of study projects through the use of CTMS or other electronic means

  • Management of investigational drug and study supplies by preparing and ensuring the accuracy of shipments of study-related materials (drug orders, study binders, clinical documents, and spreadsheets)

  • Facilitating CRF retrieval and query resolution

  • The collection, review and filing of regulatory and other documents such as site reports and FDA 1572 forms

Job Requirements:

  • B.S. Degree in Life Sciences plus 5 – 8 years of experience with clinical research.

  • Our ideal candidate is an experienced CTA who is not only familiar with the basic concepts of clinical research but has a thorough knowledge of:

  • The clinical trials process and the associated regulations including GCP and FDA regulations, responsibilities and roles required.

  • A solid working understanding of GCP requirements, clinical protocols and other essential documents.

  • A high degree of customer focus with both internal and external stakeholders and are able to handle multiple tasks and deadlines.

  • Strong knowledge of the principles and practices of computer applications in clinical database management, you will be experienced in and have a working knowledge of eTMF and CTMS, as well as advanced knowledge of Word, Excel and PowerPoint.

Apply Today! Questions? Call Justin at 714.602.1217 or email your resume to justin.lynn@kellyscientific.com

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 relevant

projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help

advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000

scientific professionals last year.

You pursued a career in science to fuel your quest for knowledge and your desire to make the world

a 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 connect

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Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females,

Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is

committed to employing a diverse workforce. Equal Employment Opportunity

is The Law.