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Cody Jacinto's Jobs

Sr. Recruitment Consultant | DOCS Global
Science & Biotech - Seattle/Portland, WA 98101

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 - Seattle/Portland, WA 98101
Site Manager, Clinical Research, CRA, Regional CRA, Sr. CRA, CRA II/III, Regulatory, Pharmaceutical, Medical Monitoring, Regional Site Manager, Query resolution, Source documents, EDC, Clinical Data, Biometrics, Sponsor, Travel, Science, Biotech
Science & Biotech - Wallingford, CT 06492

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 - Wallingford, CT 06492
SAS, SAS Programmer, Sr. SAS Programmer, Statistical Programmer, SDTM, CDISC, ADAM, Datasets, Programmer, Biostatistician, Biometrics, Clinical Data Management, Statistics, Pharmsug, Drug Safety, Clinical Research, Pharmaceutical, Biotech
Science & Biotech - Los Angeles, CA 90277

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 - Los Angeles, CA 90277
Remote, Home-Based, CRA, Sr. CRA, CRA II, Clinical Research, Site Management, Oncology, Pharmaceutical, Biotech, Trip reports, monitoring, GCP, IND, SAE, Drug Safety, CRC, Clinical Research Coordinator
Science & Biotech - Wallingford, CT 06492

Monitor progress of assigned investigator countries/sites through close contact with site staff and monitors. Disseminate appropriate site related information to involved team members. Will be point of contact for protocol-related issues. Candidate must be flexible and dependable with a BA, BS or MS degree. Successful candidate must have 3-5 years of clinical research experience, be capable of handling multiple projects and have good computer skills. The candidate must have a working knowledge of GCP/ICH guidelines, good interpersonal experience an...

View Clinical Site Manager/ CRA Job - Wallingford, CT 06492
CRA, Regional CRA, Site Manager, Sr. CRA, Clinical Research, Monitoring, CRC, Site Coordinator, Research,Clinical Project Manager, Biotech, Biopharmaceutical, Medical Publications, safety data, medical communications, scientific communication, Clinical Study manager, clinical manager, publication systems, publications
Science & Biotech - Los Angeles/San Francisco/Irvine/San Diego, CA 94101

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
Site Manager, Clinical Research, CRA, Regional CRA, Sr. CRA, CRA II/III, Regulatory, Pharmaceutical, Medical Monitoring, Regional Site Manager, Query resolution, Source documents, EDC,
Science & Biotech - North Wales, PA 19454

We are currently seeking an experienced Document Specialist for an opportunity in North Wales, PA. Responsibilities: • 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. • Manage the tracking for upcoming studies that qualify for registry/disclosure. • 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
Document Specialist, Clinical Study Associate, Clinical Trial Associate, Clinical Project, Clinical Research, Pharma, Biotech, Research, CSRs, Protocols
Science & Biotech - San Francisco, CA 94101

5 Years experience as a Statistical/SAS Programmer Industry experience required •Serves as lead Statistical Programmer to achieve milestones on one or more studies. •Develops and implements Statistical Programming Specifications and QC plans with lead statistician for one or more studies. •Works closely with study team to assure quality data and deliverables. •Provide resource estimates, timelines, and expectations to other team members. •Ensures standards at a drug program level; integrates data across multiple studies o...

View Remote/Homebased, SAS/Statistical Programmer Job - San Francisco, CA 94101
SAS Programmer, Statistical Programmer, SAS, CDISC, Pharmaceutical, Biotech, Clinical Research, Clinical Data, Clinical Data Management, Programmer, Statistics
Science & Biotech - San Francisco, CA 94101

Duties: Job Duties/Responsibilities: • Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements. • Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative. • Performs Data Capture and Quality Review for all molecules and serves as a back up for additional projects. • Identifies and initiates requests for case follow up for clinical trials and post marketing adverse events. • Works...

View Drug Safety Associate Job - San Francisco, CA 94101
Genentech, Gilead, Exelixis, Bio, Tech, Research, R&D, Safety, CLinical , DSA, Adverse Events, SAEs, Data, Clinical Data, RN, Nursing, CRN, Research, Nurse, Clinical Development, Drug Safety, Clinical Research, Medical monitor, pharmaceutical research, biotech, medical affairs, research, pharmacovigilance, Adverse event, SAE, safety narratives, CRA, monitor, drug development
Science & Biotech - San Francisco, CA 94101

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 - San Francisco, CA 94101
Biostatistician, SAS, SPSS, INFORM, Oracle Clinical, RAVE, Clinical Research, Statistician, Programmer, Clinical Data, Data Management, Bioinformatics
Science & Biotech - Fort Washington, PA 19034

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 - Fort Washington, PA 19034
Regulatory Document, Clinical Research, Biotech, Pharmaceuticals, Clinical Trials, Document Specialist, Research, Research Associate, Research assistant, CRA, Clinical Research Associate