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David Wright's Jobs at DOCS
Recruiter | DOCS
"Recruiting in the Life Sciences, Biotech, Pharmaceutical and Medical Device fields"

About Company
DOCS is a national provider of resource solutions serving the pharmaceutical, biotechnology, medical device and related clinical trials industries. Companies seeking clinical research staffing services, as well as functional outsourcing services have come to rely on our expertise.

What makes you an industry expert for DOCS?

I have been recruiting for fifteen years. I am very familiar with all positions associated with Clinical Research and what each role entails. This is essential in making the match and placing an “on target” candidate for a client. When making a placement, we strive both for a satisfied client, and a candidate that matches well to the position and is intrigued by the opportunity. I have been extremely successful in my career with placing candidates in multiple opportunities, and seeing first-hand how they have moved up the ladder in the Clinical Research industry. This is a very exciting transition to watch for a Recruiter, especially for candidates that were just beginning their careers when they started at ClinForce

 

Describe an ideal candidate for DOCS?

An ideal candidate for DOCS Global 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 area

 

What separates DOCS from its competitors?

We have been providing staffing services to the pharmaceutical and biotechnology industries for thirty years and are known throughout the United States. We have a tenured recruiting staff with strong educational backgrounds that bring a strong knowledge of the clinical trials industry.

 

What additional value do you provide your candidates?

After joining DOCS Global, our recruiters participate in best-in-class training and education classes that make them the most adept at matching qualified professionals with companies that need them. Also, our Client Services Account Management team, through frequent and meaningful communication, ensure both client and candidate satisfaction during the term of the service period, and beyond. ClinForce also provides a competitive benefits package for applicable assignment lengths.

 

What gets you most excited about DOCS?

I am proud to say that I work for DOCS Global and we are incredibly successful as a company. We are an industry leader in Clinical staffing because we are more niche focused than most companies, and hire experienced, hard-working employees. 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. Anyone should be proud to be a part of this exciting industry.

 

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.

 

David Wright's Top 3 Jobs

Science & Biotech - New York, NY 10017

This is an opportunity to work in clinical systems validation project management on behalf of one of the leading pharmaceutical companies in the world. Responsibilities: Deliverables: Follow-up and support releases for each technology/system in use User acceptance testing to be performed for respective technology/vendor systems in use Identify/write system test scripts Review of System Development Lifecycle (SDLC) documentation Evaluate Change Control Plan/Report as appropriate in close collaboration with IT Support system UAT automati...

View Sr. Manager, Pharmaceutical Clinical Systems Validation Job - New York, NY 10017
Science & Biotech - San Francisco, CA 94101

Serves as primary contact point between the sponsor and the investigational site. Assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out. Ensure overall site management while performing tria...

View Home-based Regional Sr. CRA - Oncology - Western US Job - San Francisco, CA 94101
Clinical Research Associate, CRA, ICH, GCP, Monitoring, Oncology, Cardiology, CNS, Endocrine, Infectious Disease, Immunology
Science & Biotech - Los Angeles, CA 90210

Serves as primary contact point between the sponsor and the investigational site. Assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out. Ensure overall site management while performing tria...

View Home-based Regional Sr. CRA - Oncology - Western US Job - Los Angeles, CA 90210
Clinical Research Associate, CRA, ICH, GCP, Monitoring, Oncology, Cardiology, CNS, Endocrine, Infectious Disease, Immunology