better Biotech Pharma Job at Technology

Meditech Clinicals Project Manager - Meditech Consultant Synapse SE provides consulting talent & recruiting services to Healthcare and other organizations throughout North America. Our primary areas of competency include Healthcare & Clinical Applications, Virtualization & Application Delivery, and Identity & Access Management. Founded in Minnesota during 2002 with a focus on mid-market and large enterprises, we have performed over 100 engagements in more than 30 states, Canada, and Brazil representing 80 unique

SAIC the FORTUNE 500 scientific engineering and technology applications company that is working to solve...

SAIC the FORTUNE 500 scientific engineering and technology applications company that is working to solve...

Astute Medical Incorporated, an innovative early-stage medical diagnostics company, is seeking an experienced leader in Clinical Data Management. The Manager, Clinical Data Management oversees data management operations and is responsible for ensuring that activities and processes performed are conducted according to sponsor requirements. This position works closely with the clinical operational project team. This position requires expertise in time and resource management, communications skills, project

Perot Systemsis a worldwide provider of information technology services and business solutions to a broad...more than 41 000 experienced and skilled technology and business services professionals and revenue of...be one of the world s largest technology services organizations with more than 41 000...

Perot Systemsis a worldwide provider of information technology services and business solutions to a broad...more than 41 000 experienced and skilled technology and business services professionals and revenue of...be one of the world s largest technology services organizations with more than 41 000...

Job Title Clinical Pharmacist Consultant Auto req ID 7902BR Company 336-Argus Health Systems, Inc. Site Location Kansas City, Missouri Job Description Clinical Pharmacist Consultants function independently as liaisons, interpreters, and problem solvers, bridging communication and relationships between customers and Argus associates. Clinical Pharmacist Consultants are knowledgeable about prescription drugs and the healthcare and managed care industries; they understand the health plan providers (i.e., customers

Asen Computer Associates is a nationwide provider of information technology services...

Clinical Data Manager Our client, a Successful and Thriving Medical Device company, has an opening for a Clinical Data Manager. The Clinical Data Manager is a lead member of the clinical research team responsible for data management activities across multiple trials. Activities include assisting in data entry, query processing, site management, data reporting and other data management activities in support of clinical trial projects. Perform data management activities on both paper based and Electronic data

Senior Clinical Research Associate Job Type :Full Time Career Level :Experienced (Non-Manager) Education :Master's Degree Job Description : Position Description: A successful candidate, as a member of the Clinical Affairs group, will work collaboratively with multi-disciplinary teams to support the development of new assay test systems and laboratory services in the areas of prenatal, neonatal and child health. This role will initiate, coordinate, and take responsibility for developing supporting documents

Position Title French speaking Clinical Research Associate in Canada (Contract) Location Homebased/Fieldbased Clearance Required No Daily Responsibilities Be part of a growing company that works on challenging and exciting programs of a global nature; a company known for its expertise and quality services. SRA International's Global Clinical Development unit, is a full service CRO working worldwide on Phase I - IV clinical trials in a variety of therapeutic areas. We currently have an opening for a Part-Time

Clinical Project Mgr I 160057 (NCI) Full Time Regular posted 10/30/2009 Job Category CTR - Clinical/Regulatory Req ID 160057 Able to obtain security clearance? None Currently possess security clearance? None Location Frederick, MD % Travel Relocation Yes Requirements The Clinical Monitoring Research Program (CMRP) provides direct support to the NCI's Coordinating Center for Clinical Trials, (CCCT). This position provides support to the CCCT Translational Research Support Team (TRST) in

Local NJ - PA Candidates with past Pharma industry and regulation experience Experience in designing and analyzing data from clinical pharmacology trials (phase I). At least one-year experience is required with a Ph.D. degree or 2 year experience with a M.S. degree in Statistics or Biostatistics Qualifications Experience with biomedical applications especially related to Phase I/II clinical trials, or other relevant equivalent experience. Strong communication (both writing and oral) skills and teamwork

Position Title Nurse Clinical Information Researcher (Temporary) Location US - Maryland - Rockville (MD18) (Constella) Clearance Required Yes - Not Required to Start Clearance Type POT Daily Responsibilities SRA International has multiple openings for a Nurse Clinical Information Researcher on our VAERS project. VAERS is a post-marketing safety surveillance program, collecting information about adverse events that occur after the administration of U.S. licensed vaccines. . Perform daily triage and assignment

Purpose: To support clinical trials / studies required for GS product registrations in the US and to support marketing activities. Responsibilities: Responsible for development and/or review of study documents (protocol, informed consent, etc) to assure compliance with regulatory requirements and alignment with study objectives. Responsible for implementing and facilitating clinical trials at multiple external sites, ensuring project schedules, risks and issues are managed appropriately

and the various interdependencies between operations and technology both internal and external Solid mastery of...

Job ID:2266 Back to list Clinical Data Manager Job Category: Healthcare Management Job Region: New Jersey Job Type: Consulting/Contract Description: Position reports to Manager, Data Management. Responsible for managing data management activities, interfacing with Clinical Operations on behalf of the Data Management Department to ensure that standards are communicated properly, that timelines are met according to objectives and goals and that data reporting needs

Daily ResponsibilitiesSRA International has multiple openings for a Nurse Clinical Information Researcher on our VAERS project. VAERS is a post-marketing safety surveillance program, collecting information about adverse events that occur after the administration of U.S. licensed vaccines. Perform daily triage and assignment of VAERS reports Review medical records and complete medical abstract Perform medical coding of reviewed medical records Quality Control review of medical codingRequired: DegreeBachelorsRequired

Job Description The responsible person will serve as safety lead on assigned clinical study teams and will contribute to the development of study-related documents as well as the review and analysis of safety information. This individual will be responsible for ongoing review of accumulated safety data and assist in the development and maintenance of accurate risk profiles for assigned products. Drug Safety Specialist / Manager Duties and Responsibilities Prepares relevant safety documents for company management

Clinical Research Associate II 158969 (NCI) Full Time Regular posted 10/15/2009 Job Category CTR - Clinical/Regulatory Req ID 158969 Able to obtain security clearance? None Currently possess security clearance? None Location Frederick, MD % Travel Relocation Yes Requirements Supports the Regulatory Compliance and Human Subjects Protection Branch and is located in Frederick, Maryland. Provides clinical trials research monitoring of NIAID intramural research protocols and ensures that the

Clinical Project Manager I 157578 (NCI) Full Time Regular posted 9/30/2009 Job Category CTR - Clinical/Regulatory Req ID 157578 Able to obtain security clearance? None Currently possess security clearance? None Location Frederick, MD % Travel Relocation Yes Requirements Responsible for direct project management support for select comprehensive programmatic needs of the Clinical Monitoring Research Program (CMRP), located at Industry Lane, Frederick, Maryland. Work is performed independently

Patni works with nearly fifty pharmaceutical, biotechnology and medical device firms to streamlines business processes, increase productivity, and minimize risk in the drug safety and clinical realm. Come join our team to help life science companies adhere to the stringent timelines in reporting adverse events and improve the efficiency of pharmacovigilance operations. Please email resumes to LSresumes@patni.com stating AECP as the email subject line. Position Overview: - Collect information

Job ID:630 Back to list Clinical Pharmacist Job Category: Healthcare - Allied Job Region: Florida Job Type: Full Time/Direct Hire Description: Clinical pharmacist wanted for a large Hospital in the Tampa Bay area. Will be in Inpatient Pharmacy but may have opportunity for decentralized clinical services. Requirements: Education: B.S. degree in Pharmacy with residency or Pharm D degree from accredited College of Pharmacy. Pharmacy Practice Residency or equivalent training