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i3 Open Job Positions

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Biostatistician
East Hanover, East Hanover
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - Provide statistical input ofr planning, analysis and reporting of multiple project activities. Take reponsibilities as trial statistician with minimal guidance. Provide statistical consultation. Prepare analysis plans, perform exploratory analysis of data and write statistical reports. Defend analysis and interpretations at internal and external meetings. Establish and maintain sound working relat .. Show Job Details
Clinical Affairs Project Manager
, New York
Job First Active on: Wednesday, October 28, 2009

3004 DIVISION: i3 Pharma Resourcing - The position requires substantial responsibility for implementation and follow-through of decisions/tasks dictated by Project, Project Team and manager of Clinical Operations. Performance of this position requires a minimum of 15-25% travel to investigational sites, other locations and contract research organizations (CROs). The Project Manager is responsible for protocol/amendment development (in .. Show Job Details
Clinical Data Manager
Thousand Oaks, Thousand Oaks
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - Medical Data Sciences, Data Management Primary Purpose of Position Plan, organise and supervise Data Management activities for studies/projects allocated to regional staff. Ensure global clinical data management best practices and knowledge thereof in a standardised, transparent, and efficient manner. Assume responsibility as a partner for the planning, resourcing, and execution of relevant inter .. Show Job Details
Clinical Data Manager II
East Hanover, East Hanover
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - Responsible for providing timely and prefessional 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 .. Show Job Details
Clinical Project Manager
Thousand Oaks, Thousand Oaks
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - Job Responsibilities: The Manager will be in charge of the management and daily activities of the overall projects, including the management of the investigative sites; this will include, but is not limited to, site identification, site selection, patient recruitment, and retention. The individual will have an ongoing active role communicating with Data Management, Safety Regulatory Affaires and o .. Show Job Details
Clinical Research Associate
Thousand Oaks, Thousand Oaks
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - Major Position Activities & Responsibilities: Responsible for the activities required to start up clinical trials including: protocol and CRF development; implementation; development of trial related documents and operational procedures; regulatory document collection and document filing. Responsibilities include clinical investigational site recruitment, negotiation of Clinical Trial Agreements .. Show Job Details
Clinical Research Associate
Thousand Oaks, Thousand Oaks
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - Major Position Activities & Responsibilities: Responsible for the activities required to start up clinical trials including: protocol and CRF development; implementation; development of trial related documents and operational procedures; regulatory document collection and document filing. Responsibilities include clinical investigational site recruitment, negotiation of Clinical Trial Agreements .. Show Job Details
Clinical Research Manager
, California
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - A minimum of five years relevant experience in a clinical research/drug development environment is required for a Sr. CRS position. A background in pharmaceutical industry research in the therapeutic area is preferred, but is not required. Effective oral and written communication skills are a must. The demonstrated ability to independently write Clinical Trial Protocols and Clinical Trial Reports .. Show Job Details
Clinical Safety Scientist
, New Jersey
Job First Active on: Monday, October 26, 2009

3004 DIVISION: i3 Pharma Resourcing - i3 Pharma Resourcing provides high-quality pharmaceutical personnel supported by world-class service. We draw on our clinical understanding and global resources to match the best individual for the unique needs of the job, then provide ongoing support and personal development. We have both contract and permanent positions available. We offer competitive rates and a benefits package that is second .. Show Job Details
Clinical Scientist
Jersey, Jersey
Job First Active on: Thursday, November 19, 2009

3004 DIVISION: i3 Pharma Resourcing - In-House CRA - Qualified candidates will have a bachelor's or advanced degree in life sciences and at least 5+ years experience in clinical research. Must have monitoring and office base experience in a Pharmaceutical setting. New Jersey 131 Morristown Road Basking Ridge New Jersey 07920 carol.ricciardi@i3research.com .. Show Job Details


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