better Biotech Pharma Job in New Jersey

AE CASE MANAGEMENT Receipt Execute receipt of Drug Safety phone calls and complete telephone AE form Create phone call communication logs in ARISg Triage Support the triage of cases conducted by Snr Specialist as needed Assessment - Complex Case Support the assessment of complex cases conducted by Snr Specialist as needed Assessment - Non-Complex Case Execute QC on key fields of serious cases Create key fields updates in ARISg based on QC, as needed Execute case assessment (review events, determine labeledness

The primary purpose of this position is to receive and process adverse event information from clinical trials and spontaneous reports. These reports come from physicians and other health care providers, the clinical research department, subsidiaries, legal, etc. The specialist supervises the information coordinator in the entry of the data into the computerized database. The job requires the synthesis of the event into a cogent medical narrative summary and the evaluation and entry of the data into proprietary

Review incident reports and determine if any results are unfavorable or abnormal. Document results that may include negative reaction to the drug or a negative interaction with the other drugs. Specific qualifications: : Responsible for the telephone and written communication with physicians, other health-care professionals, Sales personnel, and patients, in response to spontaneous and clinical trial Adverse Drug Reactions, Medical Devices Experiences, and technical reports associated with company products

How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Support projects and functions throughout Research & Development, including compound selection, exploratory clinical development, and late development, with decision analysis and statistical modeling. - Integrate information, opinion, and data regarding drug efficacy, safety, and market conditions to evaluate

How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Support projects and functions throughout Research & Development, including compound selection, exploratory clinical development, and late development, with model-based planning, clinical trial design, evaluations, integrated analysis, and reporting. Support decision-making by pre-clinical or clinical teams with

Our client, a pharmaceutical company located in the Northern NJ/NYC area is currently seeking qualified individuals for an In-House opportunity to work as a Clinical Research Associate. This candidate will be associated with the Virology/Infectious Disease Therapeutic area. REQUIREMENTS (please note, candidates lacking sufficient industry experience will not be considered) **Bachelors Degree in Healthcare/Science/or equivalent * 2 years of previous pharmaceutical experience RESPONSIBILITIES = Act as liaison

Shape Your Future And Ours. Schering-Plough is an innovation-driven, science-centered global health care company. Through our own biopharmaceutical research and collaborations with partners, we create therapies that help save and improve lives around the world. We apply our research-and-development platform to human prescription and consumer products as well as to animal health products. Schering-Plough's vision is to "Earn Trust, Every Day" with the doctors, patients, customers and other stakeholders

Welcome to Novartis - the company that considers its employees to be its greatest asset. Good Business. Great Opportunities. How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Think What's Possible.Support projects and functions throughout Research & Development, including compound selection, exploratory clinical development, and late development, with decision

Welcome to Novartis - the company that considers its employees to be its greatest asset. Good Business. Great Opportunities. How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Think What's Possible.Support projects and functions throughout Research & Development, including compound selection, exploratory clinical development, and late development, with model

Clinical Data Manager based out of New Jersey...

Spine Location Country State United States New Jersey City or Sales Region Summit Business...

This position is open as of 11/10/2008. Senior Biostatistician - SAS, pharmaceutical, clinical trials, Oncology Senior Biostatistician - SAS, Oncology, pharmaceutical, clinical trials Are you a senior-level biostatistician with at least 3 years experience in statistical design for clinical studies and Oncology experience? Are you looking to take your career to the next step? Then keep reading.... We are a leading contract research organization and are seeking a Senior Biostatistician with Oncology experience

This position is open as of 11/10/2008. Clinical Research Assistant Clinical Research Assistant, Medical Assistant If you are a Clinical Research Assistant with experience in Clinical Dermatology and/or Dermatologic Laser Surgery seeking part-time hours, please read on! What you'll be doing: - Coordinating and participating in a variety of tasks involved in the collection, compilation, and documentation of clinical research data. - Following protocol in a number of studies seeking F.D.A. approval.

Clinical Research Associate (CRA) - The main responsibilities of the CRA include: - Development of study specific documentation - Monitoring and/or co-monitoring of the study - Recruitment tracking and supervision of study sites - Training of study personnel at investigator s sites - Coordinating the approval process for the performance of clinical studies/notification to RBs and authorities with regard to the respective study site - Tracking and assurance of data quality at

At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance s impressive history of company stability and growth. We ve achieved these results by fostering a work environment that encourages, develops and leverages our team s capabilities. Covance s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! CLINICAL

Infectious Disease Clinical Pharmacist Job NJ Job Location Paterson New Jersey Category Pharmacy Staff Pharmacist Apply Now...

ID Clinical Pharmacist Wayne New Jersey Job Location Wayne New Jersey Category Pharmacy Staff Pharmacist Apply Now...

Clinical Research Manager In House or Home based Job Location Regional New Jersey Category Clin...

***Regional Clinical Research Associate for i3 Research- Northeast (Contract or Perm) 214178 Job Description Submit Description i3 Research is a full-service, global CRO specializing in centralnervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense focus on the unique demands of these therapeutic categories and the needs of our clients. We deliver the therapeutic science that helps our clients develop better

Clinical Trial Project Manager South Jersey New Jersey Return to Search Results Send job...

Senior Director Clinical Research Oncology North New Jersey Return to Search Results Send job...

Site Manager CRA Needed in New Jersey and Delaware In house site management with no travel involved...

AE CASE MANAGEMENT Receipt Execute receipt of Drug Safety phone calls and complete telephone AE form Create phone call communication logs in ARISg Triage Support the triage of cases conducted by Snr Specialist as needed Assessment - Complex Case Support the assessment of complex cases conducted by Snr Specialist as needed Assessment - Non-Complex Case Execute QC on key fields of serious cases Create key fields updates in ARISg based on QC, as needed Execute case assessment (review events, determine labeledness

Position Title Director, Clinical Research - Gastroenterology / Immunology Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description The Director, Clinical Research plays a key role in the design, development, implementation and conduct of clinical trials in the area of Gastroenterology/Immunology, with the initial focus on Crohn’s disease and Ulcerative Colitis. The trials in this area are global in nature (20% travel required) and focus on Phase’s II through IV

Position Title Clinical Project Manager - Respiratory / Allergy Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description The Clinical Project Manager (CPM) inGlobal Clinical Trial Management (GCTM)will function as a Study Team Leader by organizing and managing all operational aspects of the study from conception to submission while ensuring adherence to timelines. The CPM will also proactively address risk management through contingency planning. The CPM will manage critical

Clinical Project Manager The Nations top clinical research company is looking for Project Manager. A degree in Life Sciences as well as a strong background in finance is essential to this critical role. A qualified Project manager will have 5+ years of experience with CRO s where their responsibilities include the creation and adherence to strict, clinical SOPs. The Project Manager will also need to collaborate in proposal preparation, budget development and contract negations. Strong interpersonal skills

Associate Director / Director, Clinical Research CLI001889 Job Description Submit Description Merck & Co. Inc., established in 1891, is a global research-driven pharmaceutical company dedicated to putting patients first. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences and a resounding passion for improving human health. As part of our global team, you ll have the opportunity to collaborate with talented and dedicated colleagues while developing

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Project Manager Clinical Project Manager Parsippany New Jersey 0806078 Apply Online Description The Clinical...Profile Locations USA New Jersey Parsippany Organization USA02 US Clinical Development Svcs...

Clinical Research Associate CRA Senior CRA New Jersey Statewide 0805943 Apply Online Description The...Profile Locations USA New Jersey Organization USA02 US Clinical Development Svcs...

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manage competing priorities Profile Locations USA New Jersey Parsippany Organization USA02 US Clinical Development...

Profile Locations USA New Jersey Parsippany Organization USA02 US Clinical Development Svcs...

Profile Locations USA New Jersey Princeton Organization USA02 US Clinical Development Svcs...

Profile Locations USA New Jersey Princeton Organization USA02 US Clinical Development Svcs...

Profile Locations USA New Jersey Parsippany Organization USA02 US Clinical Development Svcs...

Lead Clinical Data Manager City/State:Paramus, NJ Country:United States Position #:1136 Duration:Full Time Date Posted:10/2/2008 Relocation Available:Yes Position Type:Data Management Job Description Responsible for managing data management activities, liasing with CRO's and 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 are scheduled

We are seeking a Clinical Research Associate (CRA) for a position in New Providence, NJ. Under the direction of the Study Specialist, primary duties of the CRA include: Perform implementation of monitoring and recruitment plans Design CRF completion guidelines Identify investigators and management of investigator sites Provide assistance to facilitate timely selection of investigators and sites and recruitment of patients for clinical trials globally Interact with investigators, study site personnel

A Clinical Data Manager is currently being sought for a contract position in Ridgefield Park, NJ. The Clinical Data Manager is responsible for the quality and timeliness of all data management activities for a study by preparing validation plans and chairing validation meetings. The position will prepare material for presenting at investigator meetings and will identify errors and inconsistencies in CRF data and ensure their resolution. The CDM will be responsible for study startup documents, data cleaning,

We are seeking a Clinical Research Associate (CRA) for a position in Nutley, NJ. Under the direction of the Study Specialist, primary duties of the CRA include: Perform implementation of monitoring and recruitment plans Design CRF completion guidelines Identify investigators and management of investigator sites Provide assistance to facilitate timely selection of investigators and sites and recruitment of patients for clinical trials globally Interact with investigators, study site personnel, and

We are seeking a Clinical Research Associate (CRA) for a position in Princeton, NJ. Under the direction of the Study Specialist, primary duties of the CRA include: Perform implementation of monitoring and recruitment plans Design CRF completion guidelines Identify investigators and management of investigator sites Provide assistance to facilitate timely selection of investigators and sites and recruitment of patients for clinical trials globally Interact with investigators, study site personnel, and

We are seeking a Clinical Research Associate (CRA) for a position in Cherry Hill, NJ. Under the direction of the Study Specialist, primary duties of the CRA include: Perform implementation of monitoring and recruitment plans Design CRF completion guidelines Identify investigators and management of investigator sites Provide assistance to facilitate timely selection of investigators and sites and recruitment of patients for clinical trials globally Interact with investigators, study site personnel

The Clinical Trial Manager is accountable for the day-to-day operations of 1-4 clinical trials commensurate with complexity, including trial start-up, conduct, and close-out activities. Job duties and responsibilities include: Perform job duties with minimal guidance from the Clinical Program Manager Serve as primary contact for functional area representatives in managing protocol execution Ensure accuracy and timeliness of vendor and site payments Oversee forecasting of clinical/non-clinical supplies

Job Summary We currently have an opening for a Manager Clinical Development Oncology in our Edison New Jersey location...

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g. study specific guidelines and procedures, case

Sr. Clinical Research Associate - II (2 Openings ABD) Overview: -Functions independently, and monitors one or more clinical investigations, including initiating and closing investigational centers and collecting, processing, and reviewing case report forms. -Assists with the overall planning, development, and data management of one or more clinical investigations, including the preparation, writing, and completion of required documents. -Has a thorough understanding of FDA, ICH, and GCP regulations, guidelines

Sr. Clinical Research Associate - I (2 Openings ABD) Overview: -Functions independently, and monitors one or more clinical investigations, including initiating and closing investigational centers and collecting, processing, and reviewing case report forms. -Assists with the overall planning, development, and data management of one or more clinical investigations, including the preparation, writing, and completion of required documents. -Has a thorough understanding of FDA, ICH, and GCP regulations, guidelines

Biostatistician for Central NJ Pharma Overall Responsibility Provide dedicated statistical expertise and input for the design and analysis of clinical studies in support of the Phase IIIb/IV trials. Specific Responsibilities Include: Guiding Medical Affairs in the statistical aspects of major projects. Reviewing study concepts and providing advice on the design of studies. Writing and/or reviewing statistical methods sections for Phase IIIb/IV study protocols, integrated study reports and publications

CONTRACTOR TITLE: CLINICAL OPERATIONS PROGRAM MANAGER COMPENSATION: Up to $99/W2/hr, $105/C2C/hr based on experience DURATION: 7 months ends 6/30/2009 POSITION SUMMARY: The CLINICAL OPERATIONS PROGRAM MANAGER will provide Project Manager (PMs) support for the Clinical Trial Operations Portfolio. Specifically the COPM will; (a.) develop and manage project charters, budgets and plans for complex projects (b.) assist in the identification, reporting, & resolution of risks and issues as well as

a seasoned Clinical PM for their New Jersey location...