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Manager, Medical Writing - Oncology-88
2009-09-03 23:00:00
Job Summary: The Manager, Medical Writing - Oncology is responsible for the preparation of protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), clinical sections of the CTD, integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses. The position will be responsible for hands-on writing as well as supervision of work performed by CRO/cons
Clinical Pricing Associate-89
2009-09-03 23:00:00
Clinical Pricing Associate Descriptions:Job Details: Payment processing and management. Enter payment requests into appropriate systems for payment processing against clinical contracts (JDE and/or SAP) Weekly review of payments requested to ensure accuracy and timely processing Reporting status of payments to internal clients and payees Process amendments/change request
Staff Scientist - Chemistry-i.
2009-09-03 23:00:00
Successful candidate will not only have what the required skills, but also need to pass a criminal history background check, employment verification, and education verification. Job Description: The candidate will be part of a growing group of scientists in developing and implementing robust analytical methods to support CLIENT research and development projects. The successful candidate w
Biostatistician III --at
2009-08-31 23:00:00
Successful candidate will not only have the required skills, but also need to pass a criminal history background check, employment verification, education verification, and drug screen. Provide Biostatistics support to design clinical studies and conduct statistical analysis of clinical data in compliance with applicable regulations and laws. Participate in the design and r
Biostatistician III --TI
2009-08-31 23:00:00
Position: Biostatistician III-J983 Rate: - /hr Duration: til March 2010, possibility for extension Location: Diamond Bar, CA 91765 Applies mathematical knowledge to design surveys and experiments; collects, processes and analyzes data; and interprets results. Requires 5 - 7 years experience. Provide Biostatistics support to design clinical studies and conduct
,000 RESEARCH ASSISTANT - BIOTECH --RM
2009-08-31 23:00:00
San Diego Biotech company is currently looking for a Research Assistant - to assist in investigation of an upcoming product. Exciting position for someone looking to get stared in the biotech field. Ideal candidate will have a BS in Chemistry or Biology (or related work experience) and be familiar using Word, Excel, and Outlook. Job Description - Journal entries and notes of daily
AP Specialist-07
2009-08-30 23:00:00
Duties For a portion of the time, assist with a special projectto obtain banking information from foreign vendors through research and communicationwith the vendors. For the majority of the assignment, process invoices (manual and/or electronic) into SAP. Other responsibilities as assigned based on business need. As with most accounting and finance positions, this position may require
Zoning Associate-30
2009-08-28 23:00:00
Zoning Associate Smartlink, LLC. has an immediate opening for a Zoning Associate. It is an excellent opportunity in the telecommunications field. The successful candidate will be responsible for working with local jurisdictions in planning for and obtaining zoning and permitting approvals for telecommunication projects and sites. Duties include client int
CAD Designer-31
2009-08-26 23:00:00
Job Summary: Uses CAD equipment to provide design support to Project Manager by preparing routine layouts, detail drawings, assembly drawings, sketches and diagrams. Details to include all views and dimensions necessary for manufacture. Maintain information regarding changes to database. Solid understanding of industry drafting standards and fabrication methods, specifically welded structures.
30726 Chemist II-26
2009-08-25 23:00:00
Chemist II – Analytical Chemistry – R&D – New Product Development Job Purpose: This research and development position will provide chromatography and mass spectrometry support within the cardiovascular and peripheral interventional divisions. Key Responsibilities: Perform routine and non-routine testing to support technology and product developm
Up to k! Regulatory Affairs Specialist needed!
2009-08-20 23:00:00
The Regulatory Affairs Specialist position is responsible for reviewing and filing regulatory submissions to domestic and international regulatory authorities while assuring all supporting documentation is accurate and in compliance with regulatory requirements. Pharmaceutical background preferred. Responsibilities include but not limited to: Ensure timely preparation of regula
Director, Alliance Management-89
2009-08-20 23:00:00
Job Summary: The Director, Alliance Management supports co-development partnerships and development alliances (in-licensing and out-licensing agreements), ensuring successful and effective working relationships with our partners, and working with alliances’ business leaders to deliver results. Coordinates all alliance relationship activities from contract negotiation to initial allianc
R&D Manager - Competitive Salary And Benefits-48
2009-08-20 23:00:00
This R&D Manager Position Features: Competitive salary and benefits hHgh profile position Variety of duties Great Pay to 0K Immediate need for an R&D Manager seeking competitive salary and benefits, a high profile position with a variety of duties. Familiarity with flip chip and wafer-level packaging, wafer bumping (plating, printing and others; eutec and wafer-leve
Associate Director, Medical Writing-90
2009-08-13 23:00:00
Job Summary: Position is responsible for the preparation of protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), clinical sections of the CTD (2.5, 2.7.3, 2.7.4), integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses. The position will be responsible for hands-on writing as well as supervision of work performed by CRO/consultan
ETL Developer III-21
2009-08-13 23:00:00
The ETL developer (4 - 6 years experience) is able to design, document, develop,test, install and support complex data extract, transformation and load (ETL) programs. This person will be responsible for designing, coding and testing changes various data environments. Work various teams to maintain and enhance systems. This person will work in conjunction with other IT/development and business gro
K+ PROFESSIONAL RECEPTIONIST - Great Benefits-
2009-08-13 23:00:00
This professional receptionist Position Features: great benefits flexible work schedule opportunity for advancement Great Pay to [feed_description]K Immediate need for professional receptionist seeking great benefits, flexible work schedule and opportunity for advancement. Excel, ms word and professional will be keys to success in this stable organization. Will be responsible for answ
Contract Administrator --ct
2009-08-13 23:00:00
Title: Contract Administrator Location: TITUSVILLE / NJ /08560 Assignment Length: 08/31/2009 to 12/04/2009 Rate: 30.00 - 32.00/hr Description: Manages contract compliance, vendor bid/selection, cost/benefit tracking. Responsible for vendor relationships, vendor performance management and performance evaluations. Develops and negotiates contracts. Would possess
Statistician --ia
2009-08-13 23:00:00
STATISTICIAN 809ETH OH CINCINNATI, OH 45242 Term: W2 3-4 month Pay: Applies mathematical knowledge to design surveys and experiments; collects, processes and analyzes data; and interprets results. Requires 5 - 7 years experience. Essential Requirements: Need experience as the primary author of statistical analysis plans in industry (device, pharma, biotech
Validation Supervisor-OTC Pharma-ng
2009-08-06 23:00:00
My client, a leading OTC pharmaceutical manufacturer is seeking a Validation Supervisor. Develop validation protocols and summary reports in addition to the execution of such protocol and the coordination to complete all required activities and projects. Individual must be familiar with standard concepts, practices, and procedures within the validation field. Individual will perform a variet
Manager, Risk Management-81
2009-08-06 23:00:00
Job Summary: Manager, Risk Management is responsible for managing case processing activities to ensure regulatory compliance. The Manager will triage all incoming cases to determine priority for processing and manage the workload. The Manager will participate in the review and processing of adverse event reports and also oversee the work of Clinical Safety Scientists and Senior Clinical Saf
2009-09-03 23:00:00
Job Summary: The Manager, Medical Writing - Oncology is responsible for the preparation of protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), clinical sections of the CTD, integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses. The position will be responsible for hands-on writing as well as supervision of work performed by CRO/cons
Clinical Pricing Associate-89
2009-09-03 23:00:00
Clinical Pricing Associate Descriptions:Job Details: Payment processing and management. Enter payment requests into appropriate systems for payment processing against clinical contracts (JDE and/or SAP) Weekly review of payments requested to ensure accuracy and timely processing Reporting status of payments to internal clients and payees Process amendments/change request
Staff Scientist - Chemistry-i.
2009-09-03 23:00:00
Successful candidate will not only have what the required skills, but also need to pass a criminal history background check, employment verification, and education verification. Job Description: The candidate will be part of a growing group of scientists in developing and implementing robust analytical methods to support CLIENT research and development projects. The successful candidate w
Biostatistician III --at
2009-08-31 23:00:00
Successful candidate will not only have the required skills, but also need to pass a criminal history background check, employment verification, education verification, and drug screen. Provide Biostatistics support to design clinical studies and conduct statistical analysis of clinical data in compliance with applicable regulations and laws. Participate in the design and r
Biostatistician III --TI
2009-08-31 23:00:00
Position: Biostatistician III-J983 Rate: - /hr Duration: til March 2010, possibility for extension Location: Diamond Bar, CA 91765 Applies mathematical knowledge to design surveys and experiments; collects, processes and analyzes data; and interprets results. Requires 5 - 7 years experience. Provide Biostatistics support to design clinical studies and conduct
,000 RESEARCH ASSISTANT - BIOTECH --RM
2009-08-31 23:00:00
San Diego Biotech company is currently looking for a Research Assistant - to assist in investigation of an upcoming product. Exciting position for someone looking to get stared in the biotech field. Ideal candidate will have a BS in Chemistry or Biology (or related work experience) and be familiar using Word, Excel, and Outlook. Job Description - Journal entries and notes of daily
AP Specialist-07
2009-08-30 23:00:00
Duties For a portion of the time, assist with a special projectto obtain banking information from foreign vendors through research and communicationwith the vendors. For the majority of the assignment, process invoices (manual and/or electronic) into SAP. Other responsibilities as assigned based on business need. As with most accounting and finance positions, this position may require
Zoning Associate-30
2009-08-28 23:00:00
Zoning Associate Smartlink, LLC. has an immediate opening for a Zoning Associate. It is an excellent opportunity in the telecommunications field. The successful candidate will be responsible for working with local jurisdictions in planning for and obtaining zoning and permitting approvals for telecommunication projects and sites. Duties include client int
CAD Designer-31
2009-08-26 23:00:00
Job Summary: Uses CAD equipment to provide design support to Project Manager by preparing routine layouts, detail drawings, assembly drawings, sketches and diagrams. Details to include all views and dimensions necessary for manufacture. Maintain information regarding changes to database. Solid understanding of industry drafting standards and fabrication methods, specifically welded structures.
30726 Chemist II-26
2009-08-25 23:00:00
Chemist II – Analytical Chemistry – R&D – New Product Development Job Purpose: This research and development position will provide chromatography and mass spectrometry support within the cardiovascular and peripheral interventional divisions. Key Responsibilities: Perform routine and non-routine testing to support technology and product developm
Up to k! Regulatory Affairs Specialist needed!
2009-08-20 23:00:00
The Regulatory Affairs Specialist position is responsible for reviewing and filing regulatory submissions to domestic and international regulatory authorities while assuring all supporting documentation is accurate and in compliance with regulatory requirements. Pharmaceutical background preferred. Responsibilities include but not limited to: Ensure timely preparation of regula
Director, Alliance Management-89
2009-08-20 23:00:00
Job Summary: The Director, Alliance Management supports co-development partnerships and development alliances (in-licensing and out-licensing agreements), ensuring successful and effective working relationships with our partners, and working with alliances’ business leaders to deliver results. Coordinates all alliance relationship activities from contract negotiation to initial allianc
R&D Manager - Competitive Salary And Benefits-48
2009-08-20 23:00:00
This R&D Manager Position Features: Competitive salary and benefits hHgh profile position Variety of duties Great Pay to 0K Immediate need for an R&D Manager seeking competitive salary and benefits, a high profile position with a variety of duties. Familiarity with flip chip and wafer-level packaging, wafer bumping (plating, printing and others; eutec and wafer-leve
Associate Director, Medical Writing-90
2009-08-13 23:00:00
Job Summary: Position is responsible for the preparation of protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), clinical sections of the CTD (2.5, 2.7.3, 2.7.4), integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses. The position will be responsible for hands-on writing as well as supervision of work performed by CRO/consultan
ETL Developer III-21
2009-08-13 23:00:00
The ETL developer (4 - 6 years experience) is able to design, document, develop,test, install and support complex data extract, transformation and load (ETL) programs. This person will be responsible for designing, coding and testing changes various data environments. Work various teams to maintain and enhance systems. This person will work in conjunction with other IT/development and business gro
K+ PROFESSIONAL RECEPTIONIST - Great Benefits-
2009-08-13 23:00:00
This professional receptionist Position Features: great benefits flexible work schedule opportunity for advancement Great Pay to [feed_description]K Immediate need for professional receptionist seeking great benefits, flexible work schedule and opportunity for advancement. Excel, ms word and professional will be keys to success in this stable organization. Will be responsible for answ
Contract Administrator --ct
2009-08-13 23:00:00
Title: Contract Administrator Location: TITUSVILLE / NJ /08560 Assignment Length: 08/31/2009 to 12/04/2009 Rate: 30.00 - 32.00/hr Description: Manages contract compliance, vendor bid/selection, cost/benefit tracking. Responsible for vendor relationships, vendor performance management and performance evaluations. Develops and negotiates contracts. Would possess
Statistician --ia
2009-08-13 23:00:00
STATISTICIAN 809ETH OH CINCINNATI, OH 45242 Term: W2 3-4 month Pay: Applies mathematical knowledge to design surveys and experiments; collects, processes and analyzes data; and interprets results. Requires 5 - 7 years experience. Essential Requirements: Need experience as the primary author of statistical analysis plans in industry (device, pharma, biotech
Validation Supervisor-OTC Pharma-ng
2009-08-06 23:00:00
My client, a leading OTC pharmaceutical manufacturer is seeking a Validation Supervisor. Develop validation protocols and summary reports in addition to the execution of such protocol and the coordination to complete all required activities and projects. Individual must be familiar with standard concepts, practices, and procedures within the validation field. Individual will perform a variet
Manager, Risk Management-81
2009-08-06 23:00:00
Job Summary: Manager, Risk Management is responsible for managing case processing activities to ensure regulatory compliance. The Manager will triage all incoming cases to determine priority for processing and manage the workload. The Manager will participate in the review and processing of adverse event reports and also oversee the work of Clinical Safety Scientists and Senior Clinical Saf