(US-Illinois) For more than a century, our client has been working to advance health care for people around the world. They have evolved into a diversified health care company that discovers, develops, manufactures and markets innovative products and services that span the continuum of care from prevention and diagnosis to treatment and cure. They provide total integrated solutions across the health care spectrum for some of the worlds most prevalent medical conditions, including AIDS, cancer and diabetes. Our client, a major pharmaceutical company in Lake Forest, IL is looking for a Clinical Studies Specialist - Bwith the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Member of the clinical team responsible for conducting Phase I-IV studies according to Federal Regulations and ICH guidelines. Support clinical team, primarily in tracking, organizing and filing Phase I-IV study documents according to Federal Regulations and ICH guidelines. Assist Clinical Team members in handling data queries, drug inventories, study invoice payments, enrollment tracking, and record reconciliation with site documents. Assists the CRA's with organizing and planning study investigator meetings. Bachelors degree is preferred, but not required. Candidates may also have an Associates degree, however strong work experience would be expected from these candidates. Previous experience in handling documents for pharmaceutical studies, possibly having worked at a contract research organization or site management organization would be preferred. Will also consider candidates with experience in handling documents (i.e., contracts, insurance claims, etc.) outside of the pharma industry. There is no requirement for experience in any particular therapeutic area. Looking for strong organizational and communication skills. Day to day activities include collecting documents received from clinical study sites and logging them into a clinical trial management system. Will be managing the documents received and must be able to answer what has been received to date and what is outstanding. They will also be asked to call clinical study sites and speak to site personnel about outstanding documents or issues with the documents received. May be asked to manage study contracts so that these contracts get to the appropriate parties for review and approval. May be asked to compile clinical study reports for submission to FDA. There are specific guidelines to follow in this respect. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-New Jersey) Our client, a major pharmaceutical company in Morris Plains, NJ is looking for a Intel Project Engineer with the following qualifications: Requirement Notes: THIS POSITION IS TECHNICAL. Excellent oral and written communications skills *Strong team work skills *Good problem solving skills *Ability to multi task and manage changing priorities *Minimum 3 to 4 years of relevant . Technical Expertise: Proficient in all Microsoft Office Products PowerPoint, MS Project, Excel and Word are needed skills. Qualifications: A minimum of 4 years of experience in a datacenter environment. In-depth knowledge of core Microsoft products – NT 4.0, Windows 2000 Advanced Server. Other technologies include HP Insight Manager (IMv7), SMS, IIS, SQL, VMWare. Experience in Visual Basic Scripting Edition, Kixtart, WMI, and other scripting technologies is a plus. This individual must demonstrate the ability to work with others to quickly resolve Wintel related issues. Responsibilities: This is a contractor position reporting into the Intel Services group located in Morris Plains. The individual will be expected to take direction on Wintel related projects and react quickly to service related issues. Responsibilities include communicating and coordinating with other members of the team, documenting infrastructure solutions, working with the senior Intel technical team, and some exposure to client's business units within the organization relative to technical issues and engineering projects. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
