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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

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. Key Responsibilities: 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. Communications: ensures clear written communication to clinical sites and project team members through monitoring repor...

View Clinical Trial Assistant Job - Arden Hills , MN 55112
Science & Biotech - Irvine , CA 92606

• Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions. • Creation/distribution of regulatory binders & the wet-ink signed documents binder • Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing correct...

View Clinical Study Associate Job - Irvine , CA 92606
Science & Biotech - Princeton , NJ 08541

The Clinical Trial Manager is a critical component in the execution of a clinical trial. Engagement of highly motivated clinical investigators will enable company to maximize efficient and timely delivery of clinical trials. This position is responsible for contributing to an industry leading site engagement team. The Clinical Trial Manager is responsible for providing operational expertise to sites through ownership/management of Site Engagement Strategy. The scope of this role includes the following: • Define and implement strategies for enga...

View Clinical Trial Manager Job - Princeton , NJ 08541