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Diane Brescia's Jobs at DOCS
Recruiter | DOCS
"The Strength to Deliver"

About Company
DOCS is the amalgamation of ICON Contracting Solutions and DOCS International, which together offer over 15 years of expertise in staffing the global pharmaceutical, biotechnology, clinical research and medical device industries.

Describe an ideal candidate for DOCS?

An ideal candidate should have at least two years of industry experience. They should have a solid understanding of the clinical research industry and the drug development process and be well versed in different therapeutic areas. We prefer candidates with a Bachelor’s degree or higher in the Life Sciences or other similar areas.


What separates DOCS from its competitors?

We specialize in resourcing solutions for the biopharmaceutical and medical device industries and have been a leader in our field for over fifteen years.


What additional value do you provide your candidates?

Our full-spectrum resourcing solutions extend from functional service provision (FSP), contract placement, permanent positions and executive search. Our market knowledge, global recruitment network and operational infrastructure enable us to meet our clients needs.


What gets you most excited about DOCS?

The people. This includes the people I work with on a daily basis and the clients and candidates I get to interact with. We are a knowledgeable team of recruiters that genuinely want to see employees obtain their dream job and make a difference in the world of research.


What does it take to be successful at DOCS?

We know that our success depends upon the quality of the people that represent us and perform the work. This is why our proprietary recruiting process includes insightful candidate screening, in-depth interviews, and thorough credentials verification program. Our entire recruitment process is designed to help us deliver only the best.


Diane Brescia's Top 3 Jobs

Science & Biotech - Arden Hills , MN 55112

Clinical Trial Assistant Acts as an in-house Clinical Research Associate providing support to clinical functions and site customers through site start up, enrollment, follow up and closure phases of clinical trial activities. • Site Start-Up: works across several studies to ensure all required documentation is in place in order to authorize sites for study enrollment. Partner with other team members to support patient enrollment. • Experience following SOP’s in a quality environment • Experience working with CTMS system • ICF (Informed Co...

View Clinical Trial Assistant Job - Arden Hills , MN 55112
Science & Biotech - Valencia , CA 91354

In-House Clinical Research Associate: As an In-House Clinical Research Associate you would be responsible for the following: • Monitor and report project-specific training compliance, for site and internal team. • Manage site/contact/study information using appropriate tool(s). • Review Informed Consent Form and assist with IRB submission(s) and review of IRB documentation. • Site Start-Up: work across several studies to ensure all required documentation is in place in order to authorize sites for study enrollment. Partner with other tea...

View In-House Clinical Research Associate Job - Valencia , CA 91354
Science & Biotech - Irvine , CA 92619

Clinical Study Associate This individual will provide support to the clinical study staff within Clinical Operations. Perform a variety of clinical research operations duties of a routine and technical nature in support of clinical trials. Supports project managers within the assigned clinical studies. • As directed, provides general support to the project teams which may include tracking study data, following-up with clinical sites on essential documents; assist in drafting and distributing study mailings, including study newsletters; assis...

View Clinical Study Associate Job - Irvine , CA 92619