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

About Company

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 - Plainsboro, NJ 08536

Position Summary: The Clinical Trials Manager (CTM) works closely with various internal team members and vendors as well as clinical study sites to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and budgets. This position is responsible for ensuring achievement of own or others' project goals and objectives. This person may have line management responsibilities. This person is able and willing to perform all duties or functions of subordinates. Ess...

View Clinical Trials Manager (CTM) Job - Plainsboro, NJ 08536
Clinical Research Monitoring, Monitor, CRA, Sr. CRA, CPM, Clinical Project Manager, Clinical Study Manager, Clinical Trials, Clinical Trial Manager, SOCRA, ACRP, Pharma, Biotech, Site Manager, Global Trials, FDA, Research, Pharma, Biotech, stats, SPSS, clinical statistician, clinical data manager, CDM, Manager of Biostatistics, Biostats, statistical programmer, clinical programmer, Associate Director, Biostatistics, CDISC, SDTM, ADaM, TLF, Ph.D, TLFs, TLGs, tables, listings, figures, SAP, statistical analysis plans, Biostatistician, Sr. Biostatistician, Lead Biostatistician, Manager Biostatistician, statistician, SAS, Programmer, CDISC, Sr. CDM, Senior Clinical Data Manager, EDC, Ad-HOC, SAS, MACROS, CDISC, RAVE, Medidata, INform, Query, Clinical Data Manager, Clinical Research, Pharma, Biotech, SAS, Biostatistician, Statistical Programmer, CDISC, ADaM, SDTM, EDC, Data Analyst, Data collection, Validation, Data Entry, Oracle Clinical, Medidata RAVE, InForm, Pharmacuetical, CRO, Clinical Research, CRA, Data Management
Science & Biotech - Durham, NC 27710

Summary: Expedite contract negotiation and execution by acting as a resource and liaison for the Contracts and Grants group to streamline requests to law department and avoid duplication of efforts among Contract & Grants Analysts (CGAs) and CGA management. Act as main point of contact with legal department to resolve complex legal issues while ensuring compliance with company process and strategy and subsequently disseminating information to stakeholders and team members. Principal Responsibilities: Act as liaison between Law Department, reg...

View Clinical Contracts Specialist (Remote Home Based) Job - Durham, NC 27710
remote home based, Contracts Analyst, Clinical Research Contracts, Clinical Contracts, Grants, Clinical Contract Analyst, Contract Analyst, Juris Doctor, Law degree, Lawyer, Clinical contract, Contract Law, Pharmaceutical contracts, clinical research, Document Specialist, Clinical Study Associate, Clinical Trial Associate, Clinical Project, Clinical Research, Pharma, Biotech, Research, CSRs, Protocols
Science & Biotech - San Francisco, CA 94101

Summary: The successful candidate will have the ability to present statistical methodology and trial results to various audiences, will have flexibility with deadlines, and will be able to handle high demands of early phase studies. The Project Statistician will also represent Profil interests on contracted and non-contracted studies, as needed, as they relate to statistical issues. Essential Duties and Responsibilities include the following. Other duties may be assigned at the company's sole discretion. - Represent Statistics on project teams and ...

View Biostatistician/Statistician Job - San Francisco, CA 94101
Biostatistician, SAS, SAS Programmer, Clinical Programmer, CDISC, SDTM, datasets, tables, listings, figures, graphs, PROC, ADaM, Statistician, SPSS, C#, Certified BASE, Data Management, Data Manager, Clinical Data, Clinical Data Manager, PhD Statistics, Biotech, Pharma, Technology, Programmer, SAS programming