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
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 email@example.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.