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Who I Recruit
Cody Jacinto's Jobs at DOCS Global
Sr. Recruitment Consultant |
"Clinical Research/Data, Pharmaceuticals, Biotech"
What makes you an industry expert for DOCS Global?
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 Global?
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 Bachelorâ€™s degree or higher in the Life Sciences or other similar areas.
What separates DOCS Global 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 Global?
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. Itâ€™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 Global?
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.
Summary: The Project Statistician works extensively with Clinical Data Management, Science Team, and other project team members to effectively communicate data findings to the data manager and project team, including client clinicians and statisticians. 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...View Biostatistician/Statistician Job - San Diego, CA 91911
The responsibility of a Site Manager/ Sr. Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines. Ensures that Investigato...View Remote/Home-Based Sr. CRA (Regional Site Manager) Job - San Francisco, CA 94101
Clinical SAS Programmer: Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead. Able to support multiple protocols independently and to contribute to integrated summaries of efficacy and safety. Demonstrates strong SAS programming skills; participates in protocol team and some project team interactions. Builds suc...View Clinical SAS Programmer Job - San Francisco, CA 94101
Main Function: Supports clinical trials by planning, collecting, screening, and summarizing information gathered. Responsibilities: * Plans information acquisition by identifying potential investigators, conducting pre-trial site visits, training site staff; monitoring trial drug accountability; studying clinical requirements; evaluating resources. * Collects information by searching and interviewing patients; comparing information discovered to information specifications; preparing correspondence. * Screens information by tracking patient ...View Remote/Home-Based Regional CRA/Site Manager Job - Chicago, IL 60018
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines. Ensures that Investigators are conducting ...View Sr. CRA (Regional Site Manager) Job - Los Angeles/San Francisco/Irvine/San Diego, CA 94101
We are currently seeking an experienced Document Specialist for an opportunity in North Wales, PA. Responsibilities: â€¢ Track and manage the delivery and scrutiny of Protocols/CSRs to ensure required documents are available and complete for all studies qualifying for registry/disclosure. â€¢ Manage the tracking for upcoming studies that qualify for registry/disclosure. â€¢ Notify appropriate touch point when results for a study will not be able to be disclosed within the required timeframe, including the justification for why the results w...View Clinical Trial Associate/Document Specialist Job - North Wales, PA 19454
5 Years experience as a Statistical/SAS Programmer Industry experience required â€¢Serves as lead Statistical Programmer to achieve milestones on one or more studies. â€¢Develops and implements Statistical Programming Specifications and QC plans with lead statistician for one or more studies. â€¢Works closely with study team to assure quality data and deliverables. â€¢Provide resource estimates, timelines, and expectations to other team members. â€¢Ensures standards at a drug program level; integrates data across multiple studies o...View Remote/Homebased, SAS/Statistical Programmer Job - San Francisco, CA 94101
Duties: Job Duties/Responsibilities: â€¢ Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements. â€¢ Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative. â€¢ Performs Data Capture and Quality Review for all molecules and serves as a back up for additional projects. â€¢ Identifies and initiates requests for case follow up for clinical trials and post marketing adverse events. â€¢ Works...View Drug Safety Associate Job - Carlsbad, CA 92009
Accountable to provide statistical input into the design of clinical studies, investigational plans, case report forms, database setup, edit checks, and clinical reports. Also responsible for providing consulting services to departments other than Clinical Affairs. Monitors own work performance and reports status to management. Coordinates technical decisions across organizational lines. Remains abreast of and consults on biostatistical and related advancements. Assures that quality of services meets or exceeds internal customer requirements. ...View Remote Home-Based, Sr. Biostatistician Job - Durham, NC, NC 27709
Description The Regulatory Document Specialist provides assistance as needed, for the creation, assembly, and quality control review of regulatory documents for clinical research, including clinical study reports, clinical summary sections of common technical documents (CTD), investigator brochures, protocols, and other clinical documents. Under the supervision of senior staff or supervisor, ensures quality, consistency, and conformance to department standards and appropriate regulatory guidelines for clinical documents, including clinical study re...View Regulatory Document Specialist Job - Philadelphia, PA 19019