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Cody Jacinto's Jobs at DOCS
Senior Recruitment Consultant | DOCS
"Clinical Research/Data, Pharmaceuticals, Biotech"

About Company
DOCS is a Global 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 over 8+ years of successful recruiting experience in the Clinical Research, Pharmaceutical, Biotech Industries, with a proven track record of placing both contract and permanent clinical research professionals in both clinical and data positions.


Describe an ideal candidate for DOCS?

An ideal candidate for DOCS 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 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 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. DOCS also provides a competitive benefits package for applicable assignment lengths.


What gets you most excited about DOCS?

DOCS has a strong presence in the clinical research staffing industry. We are at the forefront of providing a first class service to our clients and candidates. It’s very exciting that DOCS continues to grow our business development and adapt with our 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.


Cody Jacinto's Top 3 Jobs

Science & Biotech - Titusville, NJ 08560

Position Description: • Overseeing programming activities on an assigned project • Working with cross-functional teams • Creating SDTM and ADaM specifications • Guiding more junior programmers in the implementation of SDTMs and ADaMs • Strong experience developing MACROS and specification writing 5 or more years of SAS Clinical experience and CDISC knowledge required, Basic Qualifications • BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Li...

View Remote Home Based Sr. Statistical Programmer Job - Titusville, NJ 08560
SAS, SAS Programmer, Statistician, Statistical Programmer, CDISC, Clinical Research, TLF, ADaM, SDTM, Clinical SAS, Biometrics, Biostatistician, Pharmaceuticals, Biotech, Data Analyst, Clinical Data, Clinical Data Manager, Clinical Programmer, ISS, FDA, ICH, ISE, Analysis Datasets, PROC, CDISC Standards, Validation, Data Analysis, Clinical Data Analysis
Science & Biotech - Durham, NC 27701

Key Responsibilities include: • Identifying and resolving issues at a regional level • Collaborating with Global PM to ensure country level study delivery is aligned with the global study project plan • Contributing to study-level risk assessments • Leading and continually review regional risk mitigation activities to ensure study delivery to plan • Overseeing regional insourcing /outsourcing partner deliverables to the required standards • Partnering with Tech Services, Supplier Governance and Electronic Trial Operations to ensure regional,...

View Clinical Trial Manager Job - Durham, NC 27701
TMF, Trial master file, Clinical Research, CRA, CTS, Project Manager, Clinical Trial Manager, Global Trial Manager, Clinical Trials, Adverse events, Phase, EDC, Medidata Rave, Research Pharmaceutical, Biotech, CRO, Health, Healthcare, Clinical Trial Associate, CTA, CTS, Medidata Rave, Clinical Research Associate, Research, Biotech, IVR, CRA, In-House CRA, Sr. CDM, CDM, Clinical Research, RAVE, EDC, InForm, Clinical Data, Data Management, SAS, Programmer, Pharmaceutical, Biotech, Research, Clinical Research, Clinical Data Coordinator, GCP,
Science & Biotech - Durham, NC (RTP), NC 27701

(Senior Statistician) Job Purpose Supports teams through contributions to the design, planning, execution, analysis, and reporting of clinical and non-clinical studies, with a view toward establishing the conditions essential for determining safety, efficacy, and marketability. Complete understanding and wide application of technical principles, theories, and concepts in the statistical field. Under general supervision lead scientific development of protocols for multiple projects. Independent operational and technical leadership of mul...

View Senior Statistician/Sr. Biostatistician Job - Durham, NC (RTP), NC 27701
CDISC, SAS, R, PhD, Statistics, Biostatistics, Biostatistician, Clinical Research, Clinica Data, Rave, Mediata, Baysian, Methodology, Statistician, ADaM, SDTM, TLF, Outcomes Research, Epidemiology, Research, Clinical Research, SAS, SPSS, STATA, Epiinfo, observational research, Clinical Trials Research, Clinical Trials, CDISC