(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 County, IL is looking for a Clinical Medical Services Specialist - B with the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Provides medical support with emphasis on the intake of medical product experiences and processing standard communication requests. Acts as a liaison with Quality Assurance for product quality problems where an adverse event is involved. Works with Customer Service to provide standard information and product replacement as necessary. Provides assistance to the medical and lay community with standard information that is from the package insert or information from the standard letter database that deals with labeled and specific off-label information/indications. BS Preferred. BSN, RPh or Pharm D required. 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-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 County, IL is looking for a Medical Writer II with the following qualifications: REQIRES 3-5 YEARS OF EXPERIENCE. Prepares technical documents to support both domestic and international regulatory submissions. Incorporates text, graphs, charts, tables and statistical analysis. Proofreads, circulates, edits, assembles, inspects and duplicates product submissions. Medical Background - either BSN, RPh or PharmD preferred. 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-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 County, IL is looking for a Clinical Medical Reviewer/Safety Reviewer - C with the following qualifications: REQUIRES 5+ YEARS EXPERIENCE Responsibilities include medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, QA of data listings. May manage the activities of regional contract CRAs, and organizes the files and budgets associated with several clinical studies. Provides medical support which may include: Adverse Event Reporting - the investigation and reporting of medical product experiences, in depth investigation of medical adverse events and works with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; or Medical Communication which includes writing standard and custom responses to communication requests, in-depth assistance to the medical and lay community by responding to inquiries with medical/scientific information that is more complex and requires more data than is supplied in the package insert or the standard letter database. Off-label information would be disseminated at this level. May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and CRF completion, writing study summaries, and review protocols, study summary investigator brochures and IND annual updates for safety data verification. BS Preferred. This is a part-time position, with flexible work hours; although a minimum of 3 days is required. 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-Pennsylvania-Pittsburgh) THE PITTSBURGH TISSUE ENGINEERING INITIATIVE CALL FOR APPLICATIONS POST-DOCTORAL FELLOWSHIP IN TISSUE ENGINEERING Supported by an Institutional National Research Science Award from the National Institute of Biomedical Imaging and Bioengineering The Pittsburgh Tissue Engineering Initiative (PTEI) is pleased to invite applicants for its innovative, NIH-supported, two year Post-doctoral Fellowship Program in Tissue Engineering (TE). The fellow will pursue training in musculoskeletal TE, encompassing seven focus areas: artificial organs, bioimaging, biomaterials, bone and muscle, gene therapy, stem cell biology, and transplantation. PTEI is a unique consortium of major research institutes and universities in southwestern Pennsylvania, with linkages to biotechnology companies throughout region. Potential training sites for fellows encompass all the programs and laboratories within this network. The program is unique in that each fellow is assigned a primary and secondary mentor chosen from the member institutions (2/3 to 3/4 of the two years in the primary mentor’s lab, the rest in the secondary mentor’s lab) and based on correspondence between mentors’ expertise and fellows’ prior training and desired focus within TE. Potential mentors include M.D.s, D.M.Ds, D.D.S.s, Ph.D.s, and individuals with dual degrees. The fellowship is two years in length, with an optional third year if the mentors and fellow agree. Fellows also receive training in the ethics of research, experimental design, and statistical analysis, and enroll in a basic biotechnology commercialization and intellectual property course offered by Carnegie Mellon University. Ad hoc experiences in local biotech startup companies can also be arranged. According to NIH/NIBIB eligibility criteria, a trainee must be a citizen or non-citizen national of the U.S. or must have been lawfully admitted for permanent residence (i.e., in possession of a currently valid Alien Registration Receipt Card I-551). Non-citizen nationals are generally persons born in outlying possessions of the U.S. (e.g., American Somoa). Individuals on temporary or student visas are not eligible. Applicants with a Ph.D., M.D., and related advanced degrees are eligible. A record of scientific achievement is highly desirable, and excellent written and oral English communication skills are mandatory. Starting date is flexible and will be between November 1, 2003 and July 1, 2004 for one remaining position for this fiscal year 03-04. For fiscal year 04-05, two additional positions will be available. Competitive training stipends and health insurance are provided.
