CenterWatch

1+ months

Clinical Research Associate (Full time or contract to hire)

Kelly Services
Seattle, WA 98194
**Home Based Clinical Research Associate** **_***MUST CURRENTLY RESIDE IN SEATTLE AREA***_** **(Full time or contract to hire)**




**Seeking a full-time regional Clinical Research Associate (CRA)** **_***who is currently residing in the Seattle area***_** **. This is a home-based position.**


This is a full-service Seattle based clinical research organization (CRO). We focus on supporting clinical trials for small to mid-sized biotech, pharma and medical device companies in the early phases of clinical development. We are an employee-focused, niche service provider seeking highly skilled individuals to join our team.



For CRAs who are looking for a smaller company that puts the value of our employees first, we offer a competitive salary and innovative benefits package including an annual bonus, flexible PTO policy, a 401(k) and much more.



We are a group of dedicated, passionate people working in a fast-paced and supportive organization, who genuinely like each other and enjoy what we do. If you are an energetic and bright individual looking to make a change where you can truly be a contributor, we want to hear from you!





**Position Summary:**



Responsible for conduct and management of the clinical monitoring function of clinical trials, both directly and working with contracted providers. This position focuses on coordination of all monitoring activities required to initiate, monitor and complete clinical programs.





**Primary Responsibilities:**




+ Conduct on-site visits (Qualification, Initiation, Interim, Close-Out) to monitor study progress and assure compliance with protocol-requirements, applicable regulations, ICH/GCP and Company Standard Operating Procedures.

+ Serve as primary contact for sites, Project Managers, Clinical Data Managers, and other staff as needed for site-related inquiries and issues.

+ Act as site liaison to Sponsor Representatives, Clinical Trial Managers, and Clinical Trial Associates.

+ Prepare timely, appropriate, and accurate communication to internal and external teams, investigative site staff, and consultants.

+ Manage and track study progress on recruitment/site selection, site readiness, regulatory (IRB/EC) submissions, subject enrollment, etc.

+ Participate in project calls and provide study updates as appropriate.

+ Lead or assist with study start-up activities including the review of clinical and project-related documents as requested by management.

+ Participate in Company or Sponsor required training programs.

+ Perform necessary administrative functions (e.g., tracking and submitting expense reports, time, and attendance).

+ Maintain home office (e.g., procurement of office supplies, submission of documents).

+ Perform other duties as assigned.





**Qualifications:**




+ Minimum of 3 years of related clinical research experience. Candidates with at least 2 years of on-site monitoring experience and 1 year of oncology experience are preferred.

+ Previous experience in a small or start-up company with a remote work environment is desirable.

+ Direct experience monitoring oncology studies.

+ Bachelors degree in a life science or medical discipline, or equivalent applicable experience, is preferred.

+ Willing and capable of conducting regional travel within North America for as much as 60% of time or as required by specific study/project needs.

+ Proficiency with Microsoft Office Suite, electronic data systems, and other database programs is required.

+ Must have the ability to work independently and maintain confidentiality.

+ Excellent verbal and written communication skills and the ability to communicate effectively with all levels. This position requires the ability to work with outside agencies in a professional manner.

+ Strong organizational skills.

+ Attention to detail and accuracy is essential.

+ A working knowledge of FDA regulations, ICH/GCP and other regulatory requirements.

+ Ability to work in a fast-paced environment.










**Why Kelly** **** **?**



With Kelly, youll have access to some of the worlds highest-regarded scientific organizations
providing you with opportunities to work on todays most challenging, research-intensive, and relevant
projects. Our connections can lead you to innovative scientific pursuits youll 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 careerconnect 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
with 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 is
committed to employing a diverse workforce. Equal Employment Opportunity
is The Law.

Categories

Posted: 2019-07-15 Expires: 2019-09-19

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Clinical Research Associate (Full time or contract to hire)

Kelly Services
Seattle, WA 98194

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