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i3 Open Job Positions
Clinical Data Manager
,
New Jersey
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DIVISION: i3 Pharma Resourcing -
Responsible for providing timely and professional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be declared clean and locked according to strict performance standards. Review and contribute to the development of trial validation plan related documents and create/approve final CRF design ..
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Clinical SAS Programmer
So. San francisco,
So. San francisco
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DIVISION: i3 Pharma Resourcing -
Must have a background in Oncology!
Must have at least 5 years of SAS programming experience in supporting clinical trials; possess high level of expertise in SAS/BASE, SAS/STAT SAS/GRAPH, SAS/SQL, MACRO, ODS, SAS REPORT and SAS/CONNECT areas; and be proficient in data manipulations, report/graph generations using data steps with varies SAS functions, procedures, macros, and ODS facilities; must b ..
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Clinical Study Director - Neurology
Malvern,
Malvern
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DIVISION: i3 Pharma Resourcing -
Medical reference and medical expertise for operational strategy within the CSO for study (ies)/ registries he/she is allocated to,
- Medical consultant for projects to be proposed to the CSO
- Medical contact for interaction with physicians responsible for the project or the study at the customer level,
- Support with his/her medical knowledge and background a study or a project from business neg ..
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Clinical Trial Administrator
Wayne, PA,
Wayne, PA
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DIVISION: i3 Pharma Resourcing -
Provide efficient clinical trials administrative support to clinical programs staff responsible for management of clinical trials across Phase II - IV
· Assist with accurate Clinical Trials Management System data entry and reporting.
· Assist with clinical document generation, review and revisions.
· Assist with all aspects of study meeting organization including external Scientific Meetings ..
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Clinical Trial Associate - Oncology
,
Pennsylvania
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DIVISION: i3 Pharma Resourcing -
The primary objective and purpose of this position is to assist the International Clinical Trial Manager (ICTM)/GCPM with the global trial initiation, conduct and reporting of trial progress by coordinating assigned activites autonomously. This would include participation in CRF design, study related document development, collection of the data generated by the CRUs and generation of ad hoc status ..
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Contracts Manager
Summit, NJ,
Summit, NJ
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DIVISION: i3 Pharma Resourcing -
PREREQUISITES:
4+ years in the Phannaceutical Industry; 3+ years perfoüning clinical contracting
BA/BS degree in life sciences, business, finance or equivalent,
(MBA/MS-4+ years in the Phamaceutical Industry; 2+ years in peforming clinical
Responsibilities will include. but are not limiled to. the followine:
1. Per.fotm and nanage all activities associated with the development and execution of c ..
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Contracts Negotiator
,
Pennsylvania
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DIVISION: i3 Pharma Resourcing -
Develop contracts for review by investigator, sponsor and internal legal group.
- Negotiate contract and budget with clinical sites, and coordinate approval from sponsor.
- Communicate ongoing status of negotiations to internal project team leads and sponsor as well as maintain and update contract-tracking databases.
- Organize final signature of original contracts by investigator.
- Internall ..
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CRF Forms Designer
Summit,
Summit
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DIVISION: i3 Pharma Resourcing -
i3 Pharma Resourcing provides global professional clinical research staffing services to the pharmaceutical, biotech and medical device industries. We draw on our deep understanding of clinical trials and the resources of our parent company, UnitedHealth Group, one of the world's largest health care companies, to match the best individual for the unique needs of the job. Once that placement has be ..
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Data Extraction Manager
Falls Church, VA,
Falls Church, VA
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DIVISION: i3 Pharma Resourcing -
Our client is looking for a person, preferrably medically trained, for a database study project intended to start in spring 2010. The project will be a collaboration with the US department of defense, and consequently the data manager will need security clearance.
The person would be reviewing electronic health records of subjects with certain conditions (identified from a database) and would ext ..
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Data Manager
Thousand Oaks,
Thousand Oaks
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DIVISION: i3 Pharma Resourcing -
To lead and coordinate Clinical Data Management (CDM) activities for assigned studies. This is a regional role
based in the US or UK, which may entail some global responsibilities.
RESPONSIBLE FOR:
: Delivering of data for assigned studies
: Contributing to clinical study planning
: Ensuring that data quality meets expectations
: Ensuring that CDM deliverables are to agreed timelines
: Communicat ..
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