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CLINICAL RESEARCH ASSOCIATE- Multi-site Cancer Center Network has a position available. Will examine research protocol for patient participation, collect & maintain data, & monitor clinical trials. Ideal candidate will have strong knowledge of medical research coordination. Understanding of human research regulations, & ability to analyze & interpret data. Must be team-oriented & driven by compassion for cancer patients. Some travel. 3-5 yrs. LPN Oncology exp. required. RN pref'rd. Competitive

This position is open as of 11/3/2009. BioStatistics - BioStatistician - BioInformatics - Scientist - SAS - SPSS- Clinical Trials BioStatistics - BioStatistician - BioInformatics - Scientist - SAS - SPSS- Clinical Trials We will relocate you to New York for this position. If you are a BioStatistics with experience working on a variety of clinical research datasets, please read on! We are a pioneer in the diagnosis, treatment and research of mental illness. We are looking to add a BioStatistician to our

The candidate will work as part of a team to initiate and manage research studies in the most optimal fashion. Ensure the accurate execution of research protocols in accordance with Good Clinical Practices, HIPPA and required obligations to patient/subject, Principal Investigator, research team and the sponsor. Directly interface with patients/subjects and the Principal Investigator in support of the clinical trials. Establish liaisons within the School of Medicine, and NYU Medical Center that may include: Research

Nestled in the valley of the San Bernardino National Forest, we are just a short trip away from some of the most captivating scenery in California. Just to the north, you'll find the beautiful mountain towns of Lake Arrowhead and Big Bear, where you can enjoy year-round recreation, including skiing and boating. Travel south and visit the beach cities of Orange County and San Diego, all of which offer endless swimming, surfing and general fun in the sun. East from here is the resort city of Palm Springs, and

excelleRx, Inc. is the market leader in pharmaceutical care for niche disease markets, providing expert medication consultation and pharmaceutical distribution services. Combining proprietary technology and clinical experience, excelleRx ensures the appropriate use of medication, and thereby enhances quality of life. Caregivers from healthcare facilities nationwide rely on excelleRx to manage their patients' pharmacotherapy needs. The excelleRx mission is to use technology and clinical expertise to change the

Clinical Pharmacist Full Time This position will coordinate the implementation of a healthcare quality improvement project to improve medication safety practices and develop interventions aimed at reducing inappropriately prescribed medications in the elderly and drug-drug interactions. The successful candidate will facilitate teleconferences, monitor and document project progress and adherence to project timelines, as well as coordinate project activities with participating external organizations.

Clinical Pharmacists NEEDED!!! 3 Clinical Pharmacist positions open. 2 of these positions are considered to be float positions where the Pharmacist will be working primarily in central operations with the opportunity to work in decentralized areas. The other position, I'm looking for an Oncology Clinical Pharmacist who has completed an Oncology Specialty Residency and/or 2-3 years of experience in Oncology. We are looking for someone who will demonstrate clinically sound decision making skills and a mastery

Employment Type: Full Time Salary: Highly Competitive Shift/Hours: Variable Hours/Pay Period: 80 Date Posted: Nov 3, 2009 Job Category: Clinical Professional Note: Please read the complete description below before applying for this job. The Clinical Pharmacist provides:Pharmaceutical care including evaluation of medication orders for appropriateness of drug and dose Frequency and adequacy of monitoring Evaluation of drug interactions and allergies Therapeutic monitoring of

USresources Healthcare is a hospital staffing firm specializing in the placement of RNs, LPNs, Allied Health professionals, Pharmacy and Hospital Management in permanent positions. We are committed to excellence in taking care of the healthcare professional. We currently have an opening for a Clinical Programmer. This is a full-time position.. Job Requirements: Previous experience required. Please apply by clicking the 'apply' link on this page. For more information or a complete list of our open positions

JOB TITLE Clinical Research Associate GENERAL SUMMARY OF DUTIES Perform routine site monitoring visits, participate in site selection, site initiation and study closure activities to ensure that the conduct of the clinical trial is being conducted according to the approved protocol, amendments, company SOPs, and all regulations and guidelines. DUTIES INCLUDE BUT ARE NOT LIMITED TO: Assist in the Investigator selection and qualification process. Assists in planning and preparation of Investigator

JOB TITLE - Clinical Data Analyst GENERAL SUMMARY OF DUTIES - This position is responsible for clinical data management of SCRI clinical trials. This includes all data management activities from protocol review to the final data deliverable to the sponsor. The Clinical Data Analyst supports data management project activities according to pre-defined timelines and ensures timely completion of those projects. This position must clearly demonstrate the ability to manage multiple projects with different sponsors

JOB TITLE Biostatistician GENERAL SUMMARY OF DUTIES Responsible for ensuring that appropriate statistical techniques are used which guarantee the scientific validity and overall quality of clinical trial results. Perform statistical analysis, contribute statistical input when requested, and represent the Biostatistics function of SCRI to external partners. DUTIES INCLUDE BUT ARE NOT LIMITED TO: Perform protocol development/sample size calculation & protocol/CRF review Work cooperatively

Yoh Clinical is seeking a top-notch Senior Clinical Project Manager - IVD for a contract role with our customer. Duties: - This position is located in Raleigh/Durham, NC. - Our customer is an established clinical diagnostics company with a number of products in clinical trials and on the market. They are seeking a contract Senior Clinical Project Manager to supplement their team. - The incumbent will be responsible for the overall management of clinical trials, including protocol and study

Serve as, or assist, Study Coordinator in all facets of protocol; conduct patient and caregiver interviews, interact with families and pharmaceutical sponsors. Collect and maintain data and complete case report records; dispense medication and monitor drug log inventory; follow up on adverse events; perform lab duties, e.g. venipuncture, urine, vital signs, ECGs. Must have a medical background in placing and managing IVs. RN or LPN preferred. Complete and maintain regulatory documents. Communicate with and

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

Job Summary 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. Essential Functions and Duties - Prepares relevant safety documents for company management as well as

Clinical Research Coordinator About Us SERRG is a Georgia-based Site Management Organization that actually manages your Clinical Research Study. We target three distinct markets: the research industry; physicians; and patients. We have a vast network of Principal Investigators that have met our rigorous criteria and training. We are constantly cultivating and strengthening our network of pharmaceutical research industry leaders, Institutional Review Boards (IRB), hospitals, government and community-run

Normal 0 false false false Clinical Biostatistician- 12 months contract Pleasanton CA The Biostatistician acts as an in-house statistical consultant - Provides consulting services, analyses and statistical reports to Scientists. - This individual interacts with clients on a regular basis and translates the scientific question into statistical question, determines the necessary statistical tools and performs the data analysis. - The projects are short term and require quick turn

Applicant will work within Database Administration with Ad Hoc SAS Programmers, Integrated Review Administrator, OC DBA/Database Manager and CRF designer to meet the needs of various customers. Customers include Clinical, Programming, Data Management and medical. Applicant will be responsible for Ad Hoc SQL Programming, OC procedure programming and OC study Database Build and Maintenance. Responsibilities for this position include Programming in PL/SQL and or SQL for ad hoc reports (E.g. metric reports from

Adecco Medical & Science, a division of the world leader in the recruitment of Medical and Science professionals, has an immediate opening for a Biostatistician on a contract opportunity in Pleasanton, CA. If you are interested in this opportunity through Adecco Medical & Science, please apply now!! The Biostatistician acts as an in-house statistical consultant the departments. Provide consulting services, analyses and statistical reports to clinical areas. Work closely with programmers to provide

Clinical Pharmacist Tracking Code 216713-955 Job Description Summary: Responsible for the daily activities of the pharmacy program in all health plans. Assists with the development and execution of numerous initiatives that improve the quality or cost effectiveness of drug therapy. Required Skills Review requests from members and physicians for Prior Authorization. Assists with the analysis of drug utilization data to identify trends and develop strategies. Develops formulary monographs and recommendations

Clinical Pharmacist I Tracking Code 216606-955 Job Description Responsible for the daily activities of the pharmacy program in all health plans. Assists with the development and execution of numerous initiatives that improve the quality or cost effectiveness of drug therapy. Required Skills Review requests from members and physicians for Prior Authorization. Assists with the analysis of drug utilization data to identify trends and develop strategies. Develops formulary monographs and recommendations. Develops

Clinical Pharmacist Manager Department: Pharmacy Schedule: Full Time Shift: Day Hours: Contact Information: Contact: Laura Kearns Tel: 281-295-4240 Email:lkearns@healix.net Job Details: Something RARE and AWESOME! Immediate Opening: Clinical Pharmacist Manager The Company Join the Healix team-As the leading authority on the management and provision of parenteral services, our program enables our clinical team to provide "leading-edge" treatments in an ambulatory setting. Infusion therapy, for specific

Clinical Data Manager Job ID: HITS11091000 Clinical Data Manager - Bethesda, MD - HITS11091000 Description: Clinical Data Manager Job Id: HITS11091000 Job Description: Manage the delivery of high quality data from project start-up and planning to project execution and project closeout on several projects Independently perform project specific quality control and quality assurance tasks on all projects responsible for as well as when requested by HOIS management Ensure consistency, accuracy, and adherence

Biostatistician 12 months contract Pleasanton CA The Biostatistician acts as an in-house statistical consultant Provides consulting services, analyses and statistical reports to Scientists. This individual interacts with clients on a regular basis and translates the scientific question into statistical question, determines the necessary statistical tools and performs the data analysis. The projects are short term and require quick turn around time to deliver results

BioStatistics - BioStatistician - BioInformatics - Scientist jobs in Manhattan, NY - - - - Send This Job to a Friend Search More Jobs CyberCoders - Be Selective Location Manhattan, NY; Boston, MA

Our client is currently looking for a Clinical Research Coordinator for a contract position at their facility in Tacoma. JOB RESPONSIBILITIES: Essential responsibilities for this position include, but are not limited to: Interview patients for protocols and collects and analyzes appropriate data for recruitment purposes, determine patient commitment and obtains informed consent. Review new patient records and screens patients for eligibility for participating in research protocol. Draw blood and

JOB TITLE Clinical Research Associate GENERAL SUMMARY OF DUTIES Perform routine site monitoring visits, participate in site selection, site initiation and study closure activities to ensure that the conduct of the clinical trial is being conducted according to the approved protocol, amendments, company SOPs, and all regulations and guidelines. DUTIES INCLUDE BUT ARE NOT LIMITED TO: Assist in the Investigator selection and qualification process. Assists in planning and preparation of

USresources Healthcare is a hospital staffing firm specializing in the placement of RNs, LPNs, Allied Health professionals, Pharmacy and Hospital Management in permanent positions. We are committed to excellence in taking care of the healthcare professional. We currently have an opening for a Clinical Programmer. This is a full-time position. Previous experience required. Please apply by clicking the 'apply' link on this page. For more information or a complete list of our open positions, please visit

Our client, located in the Bangor area, is one of the country's consistently highest rated hospitals. They are expanding and are searching for an infectious disease pharmacist . This is a Mon-Fri position The Area Maine offers unspoiled landscapes, beautiful vistas, succulent lobster, stately lighthouses, outdoor adventures and much, much more. They also have a great school system and the air is clean. Housing in reasonable and you will be able to afford to live like a king! Competitive wages and excellent

Our client is currently looking for a Clinical Research Assistant for a 1-year contract position at their facility in Tacoma. JOB RESPONSIBILITIES: Essential responsibilities for this position will include, but are not limited to: *Ensure that regulatory documents are maintained and are up to date. *Ensure that all adverse events have been documented and forwarded to the appropriate principal investigator. *Review Case Report Forms for patient eligibility, protocol compliance, omissions, errors, etc. and

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

Our client is searching for two Nurse Clinical Research Coordinators to support a study in San Antonio. Candidates will be responsible to perform clinical research and patient treatment in conjunction with one or more protocols. Responsibilities: 1. Interviews patients for protocols and collects and analyzes appropriate data for recruitment purposes, determine patient commitment and obtains informed consent. 2. Reviews new patient records and screens patients for eligibility for participating in research

Our client is searching for a Clinical Research Assistant for a project in San Antonio. The candidate will be responsible to monitor the execution of clinical trials associated with specific projects and to ensure that all necessary steps are being taken. Responsibilities: 1. Ensures that regulatory documents are maintained and are up to date. 2. Ensures that all adverse events have been documented and forwarded to the appropriate principal investigator. 3. Reviews Case Report Forms for patient eligibility

JOB TITLE - Clinical Data Analyst GENERAL SUMMARY OF DUTIES - This position is responsible for clinical data management of SCRI clinical trials. This includes all data management activities from protocol review to the final data deliverable to the sponsor. The Clinical Data Analyst supports data management project activities according to pre-defined timelines and ensures timely completion of those projects. This position must clearly demonstrate the ability to manage multiple projects with different sponsors

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking a CRA to be based in Puerto Rico. The clinical research associate monitors activities

JOB TITLE Biostatistician GENERAL SUMMARY OF DUTIES Responsible for ensuring that appropriate statistical techniques are used which guarantee the scientific validity and overall quality of clinical trial results. Perform statistical analysis, contribute statistical input when requested, and represent the Biostatistics function of SCRI to external partners. DUTIES INCLUDE BUT ARE NOT LIMITED TO: Perform protocol development/sample size calculation & protocol/CRF review Work cooperatively

Masters Level Biostatistician Division of Biostatistics, School of Public Health The Division of Biostatistics in the University of Minnesota's School of Public Health is seeking an experienced masters level Biostatistician to join a team of Biostatisticians and Epidemiologists working on epidemiological studies and clinical trials involving persons with HIV or other infectious diseases (ID). Applicants should possess an M.S. in biostatistics, applied statistics, or a related field, and a minimum of one

excelleRx, Inc. is the market leader in pharmaceutical care for niche disease markets, providing expert medication consultation and pharmaceutical distribution services. Combining proprietary technology and clinical experience, excelleRx ensures the appropriate use of medication, and thereby enhances quality of life. Caregivers from healthcare facilities nationwide rely on excelleRx to manage their patients pharmacotherapy needs. The excelleRx mission is to use technology and clinical expertise to change the

UPMC Cancer Centers works in tandem with the University of Pittsburgh Cancer Institute, which comprises the academic and research activities for cancer at the University of Pittsburgh and UPMC, to offer patients the latest advances in cancer prevention, detection, diagnosis and treatment. We are currently recruiting full-time clinical research coordinators (CRCs) for a variety of specialties at the UPMC Hillman Cancer Center in the Shadyside area of Pittsburgh. The specialties include: melanoma, sarcoma

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research i3 Research is a full-service contract research organization (CRO) focused on four CORE areas: central nervous system; oncology; respiratory and infectious disease; and, endocrinology and metabolic disease

Role in EMD EMD Chemicals, Inc., a world-wide provider of innovative life science research products, is seeking a highly motivated individual with expertise in biochemistry for the position of Senior Scientist. This individual is primarily responsible for building EMDs product portfolio by identifying, developing and commercializing novel, high-value in vitro and cell-based assays for enzyme function, molecular transport, and molecular interactions. As a critical complement to a highly developed technical skill

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you

About Eliassen eClinical Solutions Division (ECSD): Our fast-growing Solutions Provider, located in Mansfield, MA and New London, CT, is a leader in electronic data management solutions for pharmaceutical, biotechnology and medical device companies. The Division s experienced data managers offer strategic consulting and technical solutions, training, documentation and implementation of clinical software systems. Respected for the industry experience the entire team offers to sponsors, the eClinical Solutions

If you are looking for a stimulating environment where discovery and development of therapies to treat cancer patients is the central goal, Seattle Genetics is interested in hearing from you! We are looking for a highly motivated individual to join our team as our Biostatistician to provide statistical support for clinical trials. MAJOR DUTIES & RESPONSIBILITIES: - Perform sample size and power calculations - Review CRFs and edit checks - Assist in developing SAP and create table, listing, and figure