better Biotech Pharma Job in New Jersey

Business Title Clinical Data Manager 1 Requisition ID 18905BR Job Category Clinical Research Locations USA - Princeton, NJ Shift 1 Job Posting At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world's largest and most respected contract research organizations. Our clients are a Who's Who of the pharmaceutical and biotechnology industry. If you're looking for a diverse and stimulating work environment, you

Business Title Senior Manager, Clinical Data Management Requisition ID 14258BR Job Category Clinical Research Locations USA - Princeton, NJ Shift 1 Job Posting 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

Sr. Principal to Associate Director Biostatistics Oncology (DG) North NJ, Major Pharma. Base salary up to $140,000 depending on experience. Description: - - Review protocols and case report forms for trial design. - Write statistical methodology of the protocol. - Prepare analysis plan and programming specifications. - Perform inferential analyses. - Write the

Job #96715: Professional Job Code:#96715 Title:Clinical Data Manager MK207475 Date Posted:09/24/2009 Job Type:Full time Job Location:Paramus NJ Job Description: The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking individuals for the following

Statistician working on trial planning and analysis activities with review. Assists project statistician in preparing development programs for new drug indications. w Provides/lead primary statistical input for clinical study design. w Provides/lead analysis planning for clinical studies. w Provides/lead statistical input to clinical study reports. w Provides statistical support to other disciplines related to clinical statistics. w Works with

Job Description: This Clinical Data Analyst II Position Features: business casual family-oriented prestigious Great Pay to $0K Immediate need for Clinical Data Analyst II seeking business casual, family-oriented and prestigious. Experience working with oracle clinical, experience working with ClinTrials and BS degree preferred will be keys to success in this well-known, dynamic, Fortune 500 organization. Will be responsible for analyzing clinical research data, data manipulation and team work for Biotechnology

We are actively recruiting for a top-notch Senior Clinical Project Manager/Director, with strong bkgd in critical care trials, for key role in highly-regarded niche CRO. This company has earned a growing reputation for excellence, efficiency and employee-friendly policy. Its client base is expanding as is its therapeutic breadth. Seek a top-notch clinical project management leader to drive challenging and important global Critical Care trials. Critical care bkgd is essential. Experience with transplant

Veridex, LLC, a member of Johnson & Johnson's Family of Companies, headquartered in Raritan, NJ, USA is recruiting for the Clinical Research Solutions Business Director. Veridex specializes in oncology diagnostics. Clinical Research Solutions (CRS) is a newly designated unit of Veridex focused on developing the research use of oncology diagnostics. CRS has two commercial laboratories dedicated to servicing pharmaceutical clinical trials - one located in Huntingdon Valley, PA, USA and the other in Enschede, Netherlands

Our Direct client in Bridgewater ( Pharma) NJ is looking for a Clinical Researcher. Please contact Nicole Racz at if you are interested in the position below. Please send a copy of your resume and what type of hourly rate you are looking for. Thanks, Nicole Clinical Researcher SHIFT DESCRIPTION : There is a possibility that this position may extend beyond 3/31/2010. DUTIES Monitors the safety profile of the registered/marketed products in collaboration with Global Pharmacovigilance and Epidemiology

Sanofi-aventis is facing the future and leading the way as the 3rd largest pharmaceutical company in the world and number 1 in Europe. Backed by a world-class R&D organization, sanofi-aventis is developing leading positions in seven therapeutic areas: cardiovascular disease, thrombosis, oncology, diabetes, central nervous system, internal medicine, and vaccines. Embrace this opportunity to join a diverse and talented group of individuals championed to take on innovation and change in our rapidly expanding organization

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

The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking individuals for the following position: Clinical Data Manager Pharmaceutical or Healthcare Industry Experience Required. Job Responsibilities: - Review CRF design.

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

Job #97887: Scientific/BioTech Job Code:#97887 Title:Clinical Research Associate - In-House (II) JJ4393 Date Posted:11/10/2009 Job Type:Full time Job Location:Skillman NJ Job Description: The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking

Integrium is a progressive employer offering competitive benefits and growth opportunities tailored to each employee s skills and qualifications. We understand our service to our clients is only as strong as our service to each other, so we strive to create an atmosphere that fosters the achievement of professional and personal goals. At Integrium, we combine cutting-edge science and practical operational management to provide high-quality clinical trial services to our biopharmaceutical clients. We provide

Kelly Clinical Research, a division of Kelly Services, is recognized as a leader in the staffing industry, with opportunities at a variety of companies. If you have experience as an In-House CRA then Kelly has an exciting 12 month temporary opportunity for you right now, talking place at a consumer products leader in the Skillman, NJ area. We provide great benefits and an opportunity to hone your managerial skills in the clinical research sector. CRA II: -Based in a client facility. -Provide clinical research

searching for contract Biostatisticians located in New Jersey to work office based at our...

Case processing quality review. Maintain and manage a system for reconciliation of ADE cases, PQCs and MIs received at US Drug Safety. Manage execution and maintenance of Safety Data Exchange Agreements (SDEAs) Receive incoming calls related to Adverse Drug Event/incident, Product Complaint information Data entry and process of adverse drug events (ADE) into Argus system for submission to regulatory authorities when required. Exchange of Safety Information with Business Partners Perform follow-up calls

Clinical Data Analyst ll Job ID: 20780 # Positions: 1 Location: US-NJ-Raritan Experience (Years): .. Posted Date: 6/24/2009 Recruiter: Parth Joshi Apply for this job: Your application choices are: Apply for this jobonline Send your resume as an attachment viae-mail Refer someone you know More information about this job: Overview: The Clinical Data Architect is responsible for the development and maintenance of the Data Capture Tools (DCT) and Data Management Tools (DMT) for the capture, loading, reviewing

Clinical Data Manager Location: Paramus, NJ Category: Information Technology Status: Temporary/Contract Reference: US_EN_2_108300_132467 Salary: N/A Posted: October 29,2009

Scientific - Clinical Research Associate - In-Hous Location: US-NJ -Skillman Classification: Technical Required Education: Some College Required Travel: Not Applicable Client: Fortune 500 Client Position Type: Contract Start Date: Immediate Duration: 12 Months Description Based in a client facility. Provide clinical research support and assistance in overseeing the conduct of clinical trials. Work to ensure that trials adhere to study protocols, applicable

Management of the clinical trial process from protocol development through study reporting. Works in matrix structure, driving delivery of clinical studies within Project Teams. Works with internal and external customers, co-ordinates internal and external resources for clinical trial planning, handles clinical project budget and ensures completion to final reporting for both submission studies and exploratory work. Other duties as necessary.. Job Requirements: BS/BA required with 5 + years experience as

The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking individuals for the following position: Clinical Research Associate -CRA II - In-House Job Responsibilities: -Provide clinical research support and assistance in overseeing the conduct

Management of the clinical trial process from protocol development through study reporting. Works in matrix structure, driving delivery of clinical studies within Project Teams. Works with internal and external customers, co-ordinates internal and external resources for clinical trial planning, handles clinical project budget and ensures completion to final reporting for both submission studies and exploratory work. Other duties as necessary. BS/BA required with 5 + years experience as Project Manager/Study

The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking individuals for the following position: Clinical Research Associate CRA II In-House Job Responsibilities: -Provide clinical research support and assistance in overseeing

Our client is a small, well-funded and growing CRO looking for a Senior Project Manager to join their clinical team on a permanent basis. This is an in-house position with excellent benefits and a lot of opportunity for growth. This person will essentially be helping to start up their own clinical team. PURPOSE OF POSITION: Management of clinical research projects. Assess and manage resources to ensure the completion of deliverables against timelines and goals. Contributes to, or manages the preparation

i3 Pharma Resourcing provides high-quality pharmaceutical personnel supported by world-class service. We draw on our clinical understanding and global resources to match the best individual for the unique needs of the job, then provide ongoing support and personal development. We have both contract and permanent positions available. We offer competitive rates and a benefits package that is second to none in the industry!. Job Requirements: At least 5 years experience in Drug Development in Pharmaceutical

Category Clinical Country United States State New Jersey City Bridgewater Job Type Regular Relocation...

Duties: Direct the utilization of Contract Research Organizations (CROs), Central Labs. and Specialty Providers to assure the delivery of quality, timely and cost-effective external resources to support the company Development pipeline. Provide significant contribution to projects, working groups, initiatives to ensure Global CRO Management is prepared to successfully respond to the changing needs & requirements - legal, operational, regulatory & financial - of our internal & external customers, worldwide.

Senior Biostatistician- Northern NJ Compensation: $85K- $115K Description: Work at a growing Pharmaceutical company as a statistician for one or more study protocols. Contribute to study design as a member of the protocol team, develop statistical analysis plans, perform complex statistical analyses, and collaborate on final analysis and submission/manuscript preparation. Requirements: Doctoral or Masters degree in Statistics or Biostatistics. Minimum

Duties: Direct the utilization of Contract Research Organizations (CROs), Central Labs. and Specialty Providers to assure the delivery of quality, timely and cost-effective external resources to support the company Development pipeline. Provide significant contribution to projects, working groups, initiatives to ensure Global CRO Management is prepared to successfully respond to the changing needs & requirements - legal, operational, regulatory & financial - of our internal & external customers, worldwide.

Project Description: Discovery Medicine Clinical Pharmacology Portfolio Manager role will provide program/project management support based on the requirements outlined for a PSAP Program Manager. The following additional requirements are: - Experienced deploying Spotfire and Pharsight - Working knowledge of clinical study initiation and execution - Working knowledge of Pharmacokinetics Data Collection Experience in Pre-Clinical areas within the Pharma industry is required. PMP, or equivalent certification

Senior Biostatistician- Northern NJ Description: - Work at a growing Pharmaceutical company as a statistician for one or more study protocols. - Contribute to study design as a member of the protocol team, develop statistical analysis plans, perform complex statistical analyses, and collaborate on final analysis and submission/manuscript preparation.. Job Requirements: Requirements: - Doctoral or Masters degree in Statistics or Biostatistics. - Minimum of 3 years of related experience

Country USA Work Location United States New Jersey Company Legal Entity USA Novartis Corporation...

Project Description: Discovery Medicine Clinical Pharmacology Portfolio Manager role will provide program/project management support based on the requirements outlined for a PSAP Program Manager. The following additional requirements are: - Experienced deploying Spotfire and Pharsight - Working knowledge of clinical study initiation and execution - Working knowledge of Pharmacokinetics Data Collection Experience in Pre-Clinical areas within the Pharma industry is required. PMP, or equivalent

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

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

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

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

A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us the most rewarding employer in our field. US Clinical Operations Training Manager Business Unit:Pharma - OncologyDivision:PharmaCompany

Job #97587: Professional Job Code:#97587 Title:Clinical Research Project Manager II JJ4300 Date Posted:10/29/2009 Job Type:Full time Job Location:Somerville NJ Job Description: The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking individuals

a Clinical Research Manager for our New Jersey location...

Clinical - Clinical Research Project Manager II Location: US-NJ -Somerville Classification: Technical Required Education: Bachelor / Diploma Required Travel: Not Applicable Client: Fortune 500 Client Position Type: Contract Start Date: Immediate Duration: 12 Months Description Principal Duties and Responsibilities (essential functions) The Clinical Project Manager: Assists in developing and managing project timelines. Ensures clinical studies are sufficiently

The Bartech Group, one of America's largest and fastest-growing staffing firms, continues to elevate the staffing industry to a higher level of thinking. Bartech Enterprise Staffing specializes in temporary and direct placement of Engineering, IT, Technical, Finance & Accounting, and Professional staff. Currently we are seeking individuals for the following position: CLINICAL PROJECT MANAGER Primary responsibility of this position is the initiation and execution of clinical trials that support the business

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We currently have exciting opportunities for Contract Regional CRAs. Therapeutic Areas: Pain Management, Vaccine, Immunology, Dermatology, Oncology, Cardiovascular, Ophthalmology Length: 1 year with possible extension Location: Home-based near HUB Airport (i.e. Los Angeles, Chicago, Atlanta, Dallas, Philadelphia, etc). Job Requirements: - Minimum 2 years field monitoring

Oracle Clinical to their team in New Jersey...

State or China Province New Jersey City Princeton Postal Code 08540 6231...

Otsuka Pharmaceutical Development and Commercialization, Inc. (OPDC) is involved in conducting all phases of clinical research and development of innovative healthcare products to address unmet medical needs. OPDC is well established in the scientific community as a globally focused organization that plays a leadership role in the research and development of Otsuka's ethical healthcare products. The Company is dedicated to the improvement of the quality of human life and health of patients around the world

Clinical Project Manager - 4300 Company: ConsignMed Job ID#: 827 # of Positions: 1 Posted: 10/28/2009 Job Type: Full Time - Contract Location: Somerville - NJ Department: Clinical Research Apply To This Job Refer This Job Return To List Job Description Location: Ethicon, Somerville, NJ Hours: 40 hrs/week approx 20% travel required 1-year contract, maximum 2-year assignment $50/hr. General Summary Primary responsibility of this position is the initiation and execution of clinical trials