Date Posted: 8/29/2008 Department: EMGM Anderw 91982 HOMERC - Research Schedule: Full Time - Regular Shift: Varied Hours: 9:00 am - 5:30 pm (varies) Job Details: - The Clinical Research Assistant will assist the coordinator and/or nurse in the conduct of clinical research trials, including basic patient screening, consenting for appropriate studies, data entry, specimen collection, processing and shipping. Word processing (data entry, spreadsheets, patient logs). Specimen processing and shipping. Interface
Job ID: RMD082908-25095211 Director, Biostatistics and Bioinformatics Job facts: Job function Research Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardJump to contact information Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity
Job ID: RMD071108-25190345 Senior Clinical Research Manager Job facts: Job function Research Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardJump to contact information Who we are: At Roche, 79,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing
Job ID: RMD082208-25095157 Manager, Clinical Research Job facts: Job function Research Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardJump to contact information Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing
Job ID: 00011733 Principal Biostatistician Job facts: Job function Development Location United States - Indiana Indianapolis Company/ Division Diagnostics Schedule Full-time Job type StandardJump to contact information Who we are: At Roche, about 80.000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each
Job ID: 00000162 Drug Safety Specialist - 12 month contract Job facts: Job function Development Location United Kingdom - England Hertfordshire Company/ Division Pharmaceuticals Schedule Full-time Job type Fixed TermJump to contact information Who we are: At Roche, 79,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity
Job ID: 00000200 Drug Safety Specialist Job facts: Job function Development Location United Kingdom - England Hertfordshire Company/ Division Pharmaceuticals Schedule Full-time Job type StandardJump to contact information Who we are: At Roche, 79,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other
Human Genome Sciences|Rockville, MD, 20849, USA|3-5
Senior Drug Safety Specialist Location Rockville, MD Job ID 2566 Employment Status Full-Time Regular Required Experience 2-5 years Required Education Bachelors Degree or Equivalent Required Travel No Relocation Available Yes Summary/Description Human Genome Sciences (HGS)is located in the Washington, DC metro area, and was founded in 1992 with the goal of creating a global biopharmaceutical company to discover, develop, manufacture, and market gene-based drugs to address unmet medical needs.
Manager of Clinical Operations-Heartland Safe Start Job Type: Part-Time Location: Chicago, IL Last Updated: 08/07/2008 Job Description: Manager of Clinical Operations - Heartland Safe Start 30 HOURS/WEEK Salary Grade: ADM 2 Summary: The Heartland Safe Start Project address the needs of very young children exposed to violence (ages 0-5) and their families in the Northside communities of Lakeview, Uptown, Edgewater, Rogers Park, and West Ridge. The project focuses on therapeutic intervention, community collaboration
Job Description: At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical
Manager, Clinical Operations JFSAP 08000722 Job Description Apply Online Description Health Net, Inc. (NYSE: HNT) is among the nation s largest publicly traded managed health care companies. Health Net s mission is to help people be healthy, secure and comfortable. The company s POS, HMO, insured PPO, behavioral health and government contracts subsidiaries provide health benefits to more than 7 million individuals. For more information on Health Net, Inc., please visit the company s Web site atwww.healthnet
Supervisor-Clinic Ops/Departments Job ID: 18603 Division: Kauai Medical Clinic Department Name: Operations Location: Lihue, HI US Job Type: Full Time Regular Shift: Day/Eve # Hours per Shift: 8 Shift Hours: 8am-5pm Work Days: M-F Education: Bachelors Degree or Equivalent Category: Nursing-Management Bargaining Unit: Non-Bargaining Position Summary: DISCOVER - EXPLORE - ENJOY this outstanding opportunity withHawaiiPacific Health! Apply today and discover your next rewarding career experience! Find your potential
Clinical Data Manager 2 Job ID: HOIS07081002 Clinical Data Manager 2- Bethesda, MD - HOIS07081002 Description: Clinical Data Manager 2 Job Code:HOIS07081002 Job Responsibilities: Management of clinical data and study documents, including entry of data into clinical data management systems, to support clinical research team needs. Must have a thorough understanding of clinical research protocols, data collection requirements and methodologies.Must be able to recognize clinical values and abstract data from
Manager, Clinical Operations - Franchise Leader- US Biologicals Requisition ID: 50546 Position: Full-Time Regular Open date: Aug 13, 2008 2:58:05 PM Functional area: Clinical Location: King of Prussia, Pennsylvania Required degrees: Bachelors Degree Experience required: 7 years Relocation: No Basic qualifications: Bachelor's degree or equivalent. Major course of study in Science or Health related field. 7yrs experience in clinical study management. Track record in leading clinical operations teams in delivering
Clinical Research Associate Requisition ID: 49670 Position: Full-Time Regular Open date: Jul 1, 2008 5:31:00 PM Functional area: Clinical Location: NJ, NYC metro area, New Jersey Required degrees: Bachelors Degree Experience required: Not Indicated Relocation: Not Indicated Basic qualifications: 4 year BS/BA degree with 2 years site monitoring or equivalent experience preferred; OR - 3 year (e.g., RN) or 2 year Associate degree with a minimum of 4 years site monitoring experience. - Ability to proactively
GlaxoSmithKline|King of Prussia, PA, 19406, USA|>2
Clinical Development Manager(s), Biologicals Requisition ID: 49639 Position: Full-Time Regular Open date: Jun 9, 2008 3:20:29 PM Functional area: Clinical Location: King of Prussia, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Not Indicated Basic qualifications: MD or PhD with ability to independently evaluate clinical research questions. Sound scientific background required to critically evaluate all scientific aspects of vaccine clinical development and make sound clinical
Manager/Director Clinical Development - Respiratory Requisition ID: 47124 Position: Full-Time Regular Open date: Feb 5, 2008 8:38:37 PM Functional area: Clinical Location: RTP, North Carolina Required degrees: MD Experience required: 2 years Relocation: Yes Basic qualifications: Medical Degree (MD) with demonstrated record of accomplishment in clinical medicine and/or pharmaceutical industry clinical development phases II-IV. Respiratory therapeutic area experience essential. Good communication, influencing
GlaxoSmithKline|Los Angeles or San Diego area, CA, USA|>4
Clinical Research Associate Requisition ID: 48882 Position: Full-Time Regular Open date: Apr 28, 2008 4:46:41 PM Functional area: Clinical Location: Los Angeles or San Diego area, California San Francisco/Northern California Region, California Required degrees: Bachelors Degree Experience required: 2 years Relocation: Not Indicated Basic qualifications: Degree Requirements - 4 year BS/BA degree with 2 years site monitoring or equivalent experience preferred; OR - 3 year (e.g., RN) or 2 year Associate degree
Director Clinical Development Requisition ID: 47244 Position: Full-Time Regular Open date: Mar 12, 2008 6:17:43 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Not Indicated Basic qualifications: MD Degree, and a minimum of 2 years of industry and or academic experience required Physician with current medical license in the US. Training in medical oncology, radiation oncology, pediatric oncology or surgical oncology is required
Director, Clinical Development-Oncology Medical Affairs Requisition ID: 46764 Position: Full-Time Regular Open date: Jan 17, 2008 9:40:36 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: Not Indicated Relocation: Yes Basic qualifications: Medical Degree (MD) with demonstrated record of accomplishment in clinical medicine and/or pharmaceutical industry clinical development II-IV. Preferably US Board Certification in hematology, oncology, pediatric
GlaxoSmithKline|King of Prussia, PA, 19406, USA|>3
Director Clinical Development-Musculoskeletal Diseases Requisition ID: 46118 Position: Full-Time Regular Open date: Nov 30, 2007 8:59:38 PM Functional area: Clinical Location: King of Prussia, Pennsylvania Required degrees: MD Experience required: 3 years Relocation: Not Indicated Basic qualifications: Medical Degree and a minimum of 3 years drug development experience within the pharmaceutical industry. Preferred qualifications: Board certification/eligibility Details: . The Clinical Development Physician
Manager/Director Clinical Development - Oncology MDC Requisition ID: 44574 Position: Full-Time Regular Open date: Aug 13, 2007 6:31:53 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Yes Basic qualifications: MD degree with Board Certification. Preferred qualifications: MD degree with Board Certification in medical oncology, pediatric oncology or radiation oncology; or experience with supportive care drug develpment; or experience
Director/Manager Clinical Development - Oncology MDC Requisition ID: ONCOLOGY Position: Full-Time Regular Open date: Sep 27, 2006 12:54:37 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Yes Basic qualifications: Experience as a Principal Investigator and/or Co-Principal Investigator preferred. Pharmaceutical industry experience highly desirable. We are seeking an Oncologists with deep patient, molecule and disease insight to
Job No: 2008-0877S Job Title: Clinical Research Assistant Department: Lombardi Cancer Center Grade/Level: 07-- $ 34,653.84 Date Posted: August 04, 2008 The Clinical Research Assistant will perform the operational aspects of the Clinical Molecular Epidemiology Shared Resources (CMESR) by recruiting, interviewing and collecting biological specimens from cancer patients and controls. Phlebotomy experience or willingness to learn required. Coordinating between patients and laboratory work. 1) the identification
Job No: 2007-0981S Job Title: Clinical Research Assistant Department: Lombardi Cancer Center Grade/Level: 06$ 25,049.60-- $ 32,564.48$ 12.02-- $ 15.66per hour Date Posted: April 24, 2008 The incumbent will assists the Clinical Research Nurse in the collection and entering of data into appropriate format utilizing appropriate databases and forms. Assists the Clinical Research Nurse in obtaining and scheduling appropriate tests that are eligibility requirements for specific studies. Assists RN as a point
Job No: 2007-0802S Job Title: Clinical Research Assistant Department: Lombardi Cancer Center Grade/Level: 07$ 26,656.80-- $ 34,653.84$ 12.22-- $ 15.66per hour Date Posted: August 10, 2007 The incumbent will assist the PI to manage the daily activities of laboratory research, under the direct supervision of the Principal Investigator. Responsible for ordering research supplies and laboratory safety issues. Participate in research in cancer prevention and identification of biomarkers of cancer risk. The
Associate Director, Clinical Research Trials Requisition ID 12556 Working Location Cambridge, MA Required Education See Description Required Travel No Position Description Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme Corporation has been selected by FORTUNE Magazine as one of the "100 Best Companies to Work For in 2007
Clinical Research Medical Dir Requisition ID 13123 Working Location Cambridge, MA Required Education See Description Required Travel Yes Position Description Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme Corporation has been selected by FORTUNE magazine as one of the "100 Best Companies to Work For in 2006 in the United
Director, Biostatistics Requisition ID 12851 Working Location Cambridge, MA Required Education See Description Required Travel No Position Description Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme Corporation has been selected by FORTUNE Magazine as one of the "100 Best Companies to Work For in 2007 in the United States
Clinical Research Director Requisition ID 12089 Working Location San Antonio, TX Required Education Bachelors Degree Required Travel Yes Position Description Director Clinical Research The Director of Clinical Research, Oncology develops long and short-term planning strategies to ensure effective achievement of clinical affairs/business objectives and assists in setting organizational structure and systems to maintain the direction of clinical development. This position translates clinical research concepts
Clinical Research Associate II Requisition ID 12575 Working Location Cambridge, MA Required Education See Description Required Travel Yes Position Description Experienced Clinical Research Associate (CRA) needed for cardiovascular study(ies). One of the primary responsibilities is the support of activities involved in the conduct of the clinical study(ies) which includes on-site monitoring from initiation through close out of the study as well as oversight/support of trial conduct for external monitors
Associate Director, Clinical Research Requisition ID 12593 Working Location Cambridge, MA Required Education See Description Required Travel No Position Description Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme Corporation has been selected by FORTUNE Magazine as one of the "100 Best Companies to Work For in 2007 in the
Clinical Research Medical Dir Requisition ID 10993 Working Location Cambridge, MA Required Education See Description Required Travel No Position Description Position description not currently available. Please contact your HR Business Partner or Recruiter for further details.
General Dynamics|Falls Church, VA, 22047, USA|10-15
Job Title Biostatistician Job ID Number 145567 Company General Dynamics Information Technology Location Falls Church, VA Job Category Engineering Job Description General Dynamics Information Technology is a top-tier IT integrator that provides information technology, systems engineering and professional services to customers in the defense, intelligence, homeland security, federal civil and commercial sectors. With 16,000 professionals worldwide, the company has the customer knowledge, domain expertise and proven
Clinical Project Manager (CPM) Business Unit: GE Healthcare Function: Engineering/Technology Location: Princeton, NJ Job #: 839230 Posted: Aug 06, 2008 Job Description:Responsibilities The Clinical Project Manager will assume the Study Team Leader role for one or more (multi-center) studies and provide the study team with overall leadership and direction for the deliverables of a successful completion of a clinical study program. Primary responsibilities include: Write clinical protocols and study reports
Senior Clinical Data Programmer Business Unit: GE Healthcare Function: Engineering/Technology Location: Hillsboro, OR Job #: 833733 Posted: Aug 28, 2008 Job Description:Responsibilities Provide complex clinical data analysis and reporting related services specific to the needs of internal and external customers. This position facilitates the analysis and critical thinking around methods of data extraction and analysis of clinical EHR data to support the improvement of quality outcomes and clinical study
Clinical Project Manager (CPM) Business Unit: GE Healthcare Function: Engineering/Technology Location: Princeton, NJ Job #: 836408 Posted: Aug 04, 2008 Job Description:Responsibilities The Clinical Project Manager will assume the Study Team Leader role for one or more (multi-center) studies and provide the study team with overall leadership and direction for the deliverables of a successful completion of a clinical study program. Primary responsibilities include: Write clinical protocols and study reports
Clinical Data Coordinator Department: Cardiac Cath Lab Schedule: Shift: Hours: 20 hours per week - no weekends Job Details: - Certification from the Maryland Board of Nursing - Experience is preferred REQUIRES: Current Maryland Reqistered Nurse License and BSN. Data collection, performance improvement and registry experience preferred. Computer skills required, including excel.
University of Chicago Medical Center|US - IL, Chicago, 60601|0-2
The University of Chicago Hospitals is consistently ranked as one of the most progressive and prestigious academic medical centers in the nation. To continue our reputation for excellence, were committed to recruiting and retaining the most skilled and caring professionals in the industry. Branch: Pharmacy Department: 377731 Comer Peds Employment Type: Full-Time Hours Per Week: 40.00 Area/Specialty: Pediatric Description: The University Of Chicago Medical Center (UCMC) has been at the forefront of medicine
** Clinical Applications Pharmacist [ *CB15585 ]** In addition to functioning as a clinical pharmacist, this position is responsible for the coordination of special pharmacy services and support as designated by Pharmacy Management. The pharmacy clinical applications coordinator is responsible for ensuring the functionality & integrity of drug databases and medication-related applications. Ensures functionality and integrity of drug databases and medication-related applications ? Responsible for the assessment
** Clinical Pharmacist I [ 15748 ]** Our Place Now you’re ready for even greater things. Imagine: the opportunity to help shape a brand new hospital and create an environment that places the patient first! Imagine: the chance to expand your role, take on new responsibilities and be a part of an exceptional team. That’s the extraordinary opportunity offered byExempla Good Samaritan Medical Centerand the other members of Exempla Healthcare: Saint Joseph Hospital and Lutheran Medical Center. Exempla
Clinical Project Manager Location: Irving TX - National Service Center # of openings: 1 Description About the Company: Examination Management Services, Inc is a national firm that provides a variety of risk management services to the insurance and business communities. We are customer driven and technology focused, with a commitment to providing cutting edge business solutions and service excellence to our customers. About the Opportunity: EMSI is seeking a full-timeClinical Project Managerto work in our National
New Position - Clinical Research Manager Job Code : 1417 Division/Department : CARDI Location : Plymouth MN US 55442 Travel Required : None Job Type : Full Time Career Level : Manager (Manager/Supervisor of Staff) Education : Bachelor's Degree Category : Biotechnology and medical device Job Description : At ev3 we’re committed to developing innovative endovascular technologies for coronary, peripheral and neurological applications. Creative, competent people with a passion for enhancing healthcare around
Job Advertised by Pharmadiversity Job Board - Covance is a leading supplier of drug development services to the biotechnology and pharmaceutical industries. As an integral part of these partnerships, our employees make a difference in the lives of millions. With state-of-the-art Clinical Research Units, Covance has helped hundreds of drug development companies progress their compounds from preclinical to proof-of-concept studies. Each Clinical Research Unit has a dedicated team of professionals, including
Discover PPD:Our careers Home pageOur benefitsOur locationsOur people At PPD, you'll have the freedom to try new ideas and the ability to do something truly great. In our environment, innovation is encouraged. That's why the world's leading pharmaceutical and biotechnology companies come to us for discovery and development services. And why PPD is the best choice for you and for your career. Senior Clinical Research Associate (home based) Requirements The Senior Clinical Research Associate performs
This position is NonExempt. Hours over 40 will be paid at Time and a Half. Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new
The US Federal Government has posted the following job vacancy: Job Title: CLINICAL PHARMACIST Agency: Department Of Veterans Affairs - Veterans Affairs, Veterans Health Administration Location: BALTIMORE, MD Deadline: 10/4/2008 Job Function: Pharmacist Please review the entire vacancy announcement by clicking the JOB INFO link or by visiting: http://federalgovernmentjobs.us/jobs/Clinical-Pharmacist-1062292.html ...
Company Information: Breakthrough Careers! A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results, not formality
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Companys strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertexs product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection. The Sr. Clinical Project Manager is responsible for the planning, implementation
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Companys strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertexs product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection. The Clinical Project Manager is responsible independently managing multiple clinical