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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 - San Jose, CA 95101

We have a very well established pharmaceutical client located by SFO airport and they are looking for people to work in Pharmacovigilance/Drug Safety in triage workflow, intake, submissions and drug safety quality. Responsibilities: Perform QC of the data entry against source documentation, and will assess the case for completeness, accuracy and compliance with data entry conventions as specified in SOPs and/or Process Documents. • Case QC will be documented within the Global Safety Database with date of QC, and identifiers of the person th...

View Pharmaceutical Drug Safety/Pharmacovigilance Sr. Specialist - SF Bay Area Job - San Jose, CA 95101
Drug Safety, Pharmacovigilance, RN, Nurse, SAE's, Serious Adverse Events, PSUR, DSUR, Queries, MedDRA, Argus, Triage, ICSR, ArisG, Clintrace, Drug Coding, Intake, Submissions, Case Registration, Case Receipt
Science & Biotech - Philadelphia, PA 19101

This is a new role for the pharmaceutical company where they are looking for a Manager who can help them to prepare for Inspection Readiness. They are filing several new products with the FDA this year and want to have someone who has had experience preparing for FDA, MHRA and other regulatory authority audits associated with filing new products. They want a Project Manager to help them to organize this but this person has to have had Quality Management experience. Summary/Scope: Lead program teams through the activities of preparing for wor...

View Home-based Pharmaceutical Sr. Manager, GCP Clinical Quality and Regulatory Management Job - Philadelphia, PA 19101
GCP, Good Clinical Practices, QA, Quality Assurance, Auditor, Clinical Research, Clinical Trials, ICH, Pharmaceutical, SOP's, Regulatory Compliance
Science & Biotech - San Francisco, CA 94101

We have a very well established pharmaceutical client located by SFO airport and they are looking for people to work in Pharmacovigilance/Drug Safety in triage workflow, intake, submissions and drug safety quality. Responsibilities: Perform QC of the data entry against source documentation, and will assess the case for completeness, accuracy and compliance with data entry conventions as specified in SOPs and/or Process Documents. • Case QC will be documented within the Global Safety Database with date of QC, and identifiers of the person th...

View Pharmaceutical Drug Safety/Pharmacovigilance Sr. Specialist - SF Bay Area Job - San Francisco, CA 94101
Drug Safety, Pharmacovigilance, RN, Nurse, SAE's, Serious Adverse Events, PSUR, DSUR, Queries, MedDRA, Argus, Triage, ICSR, ArisG, Clintrace, Drug Coding, Intake, Submissions, Case Registration, Case Receipt