Looking to Stay Occupied While Your Spouse is Deployed?
2012-12-01 12:50:05
Why not start a great “At Home” business that can bring your family the financial security you deserve? Come and see if this is for you! No obligation and it costs NOTHING to check it out. Visit... ... Read more »
Attention Military Family Members
2012-11-01 11:57:50
Take the boredom out of your assignment by starting a career right now that can last a lifetime. We can show you how to be a “Stay at Home” worker if that’s what you want. Work when you want and... ... Read more »
Are You Sick of the Office Politics?
2012-11-01 11:52:37
So was I! Then I found a group of professional women who work together on line. There are no parties, no selling, and no over-head. Come check us out! You won’t be wasting your time. Visit... ... Read more »
Are You a Frustrated Working Mom?
2012-10-02 01:13:26
Are Your Boss’s Priorities Just Not in Line with Yours? Are you being told by your boss that you must put work above your families’ needs? Be able to walk away from that stressful job where you... ... Read more »
Do You Fear Your Main Income Will Disappear?
2012-09-01 08:58:08
Work without the hussle of the morning commute and office politics. Work right at home. We need women who are independent and driven to succeed. Are you this woman? If you believe you are then... ... Read more »
Take A Step Outside Of The Box
2012-09-01 01:34:47
Have you always liked the idea of a home-based business but were not sure how to make it work? We work with a very respected company which has an impeccable financial record. Our marketing team will... ... Read more »
Are You Tired of that Credit Card Debt?
2012-05-02 06:52:05
Are you wondering how to get out from under that Credit Card debt? Would extra monthly income help to get rid of those bills? We can help you generate that extra monthly income without selling... ... Read more »
Take Charge of Your Life and Change Your Stars
2012-05-02 06:46:06
Own your own business and take charge of your life! We offer a professional, corporate-like home-based opportunity to earn part time to full time income. Through our online training system and support... ... Read more »
2012-05-02 12:48:23
Take a deep breath and let us show you..... How to beat the recession! Stop living paycheck to paycheck. We can help you succeed at your home based business. We will provide you with - Free... ... Read more »
2012-04-03 01:07:57
There is No Limit to Your Financial and Personal Success Instead of working for someone who will determine what your worth to them, start your very own home business where there is no limit to the... ... Read more »
2012-04-03 01:07:10
Stop Delaying the Inevitable! The Inevitable? Your Success of course! You CAN be successful; you just don’t know how…..let us help. Just think, a flexible schedule, very little cost... ... Read more »
SQL/Database Engineer - Early Startup With Equity
2012-02-07 10:19:17
I am working with 2 startups. Each has a need for a very database centric engineer that enjoys working with customers. Part of the role will be pre sales and part of the role will be post sales. As with most client facing roles, these roles will pay very nicely. Both companies are about 20 employees and are at the stage where they have revenue coming in the door. JAVA/Linux/Some C/C++ is nice. SQL and database familiarity is a must. Linux clustered servers. Both companies are dealing with massive amounts of data and helping their clients solve the problems that come along in that world. If interested in hearing about the job(s) please respond to this posting or reach out to me at bbyers AT resourcetp DOT com. You can also find my profile on LindedIn if you want to read a bit about me... Feel free to link to me on LinkedIn. I link with all engineers that ask me to link and use linked in as a way to publish some of the hottest roles I am working on. Thx! Brent Byers ... Read more »
Java/ WebSerice Developer with PHP & Perl Experience -
2012-02-07 10:19:17
We are currently looking for Java/ WebSerice Developer with PHP & Perl ExperienceRequired Technical Skills are:Java, JWS/Axis2 (strong, 3+ years of project experience)SQL (strong, 3+ years)PHPPerl (strong, 3+ years) ... Read more »
Windows / Linux Server Support, A+
2012-02-07 10:19:17
For this position with a world-renowned computer manufacturing company, you will be performing a wide variety of server support activities in a large-scale, high-performance computing environment. Primary responsibility will be supporting OS related issues requiring OS rebuilds. Your responsibilities will include: Analyzing desktops, hardware, software, and operating systems Performing backups, archives, and recoveries Building machines from scripted images Identifying, diagnosing, and resolving issues Creating/maintaining documentation Working with vendors for warranty issues ... Read more »
2012-02-07 10:19:17
Job Description: RF circuit prototyping to 6GHz -Layout of printed circuit boards (PCB's) simple two-sided RF circuits. -Generation of Gerber artwork files using commercial CAD programs. -Acquisition of components. -Mechanical assembly. -Circuit bringup & debug. Characterization of RF Components -Devices: -Amplifiers -Variable attenuators -Baseband/IF circuits -Mixers -RF Passives -Couplers -Frequency dividers -Test Types -Gain -IP3/IP2 -Output power -Noise figure -Return loss -Harmonics -Test Equipment: -Spectrum analyzers -Network analyzers -RF signal sources -Phase noise analyzer -Noise figure analyzer Desired Skill & Experience B.S. EE ... Read more »
2012-02-07 10:19:17
Senior .Net Developer Job Description Upgrade, enhance and regression test a set of ASP.Net (using VB) web-based tools and reports to accommodate a new data model Deliverables: • Curriculum Standards Search Tool with multi-format Export Tool (PDF, MS Word, XML, Excel) • Web service for Curriculum Search • Add/Edit Curriculum Standards Tool • MCAS test items Question Search • MCAS test items loading tools including XML import and standards matching • Test Item Analysis Report • *All code MUST be written in ASP.Net (using VB)* • Manage Full-Life Cycle of project from analyzing business requirements, developing and testing software through production, deployment and change control • Meet scheduled delivery dates as defined by project manager • Troubleshoot, debug and optimize code for performance • Communicate effectively with product stakeholders and project team Qualifications and Experience: • 4+ years of hands-on experience as an ASP/.net developer using associated technologies (HTML, CSS, JavaScript, AJAX, Visual Basic, ADO, COM and ODBC). • 4+ years working with Microsoft IIS on Windows server platforms. MCSE Preferred. • Solid understanding of OOP methodology using both MS SQL and Oracle Databases. Ability to write queries and perform general DBA tasks such as DTS. • Ability to load and Transform XML into a relational database. • Ability to review/proof all code to ensure error-free functionality within all targeted browsers. • Good understanding of page flow, user interface design and navigation structures • Must be creative and resourceful, a self-starter and highly motivated. Able to work independently, while remaining an effective and efficient member of cross-functional teams • Must be highly organized, with excellent follow-through, multi-tasking and problem solving skills • Excellent oral and written communication skills Deliverables Curriculum Standards Search Tool with multi-format Export Tool (PDF, MS Word, XML, Excel) Web service for Search Add/Edit Standards Tool MCAS test items Question Search MCAS test items loading tools including XML import and standards matching Test Item Analysis Report *All code MUST be written in ASP.Net (using VB)* ... Read more »
Sr. Manager / Associate Director, Regulatory CMC
2012-02-07 10:19:17
Company Information: At Millennium: The Takeda Oncology Company; "We Aspire to Cure Cancer". Millennium is a leading biopharmaceutical company focused on oncology that combines the agility, ideals and camaraderie of a start-up with the resources of Japan's largest pharmaceutical company. The result is a creative, entrepreneurial environment where quality science and making a difference in patients' lives are the priorities. Here, employees who share a drive and commitment to innovation for the benefit of oncology patients find their ideas, experience and contributions are valued and rewarded. Millennium offers great benefits, a friendly and respectful atmosphere, and a culture that promotes flexibility between work and life and encourages employees to give back to their community. Position Summary: This individual is expected to provide leadership within Regulatory Affairs and will be responsible for actively contributing to the development and implementation of CMC regulatory strategy for large molecule products in development as well as coordinating all aspects of CMC regulatory submissions relevant to their assigned projects or programs. This person will serve as the regulatory CMC representative on relevant project teams, and as the regulatory CMC contact with FDA. Duties and Responsibilities: Develop global CMC regulatory strategy for development products. Direct management of assigned large molecule development programs. Drive all CMC submission activities (IND, CTA, NDA, BLA) and health authority interactions (meeting requests and briefing documents). Represent Regulatory Affairs at various project team and working group meetings. Assess and communicate CMC regulatory requirements to ensure all development activities are in compliance with applicable regulations and guidelines. Expected to develop and manage project timelines as well as have the ability to multi-task. Monitor changes to development plans and provide regulatory guidance to teams to bridge changes into the clinic. Contribute to the development of equivalency protocols, validation protocols, and stability protocols. Ensure the quality and content of all submissions to health authorities. Liaise with partnering companies to ensure regulatory alliance. Act as direct point of contact with FDA and other regulatory authorities for CMC related issues. Mentor and coach junior regulatory staff and other team members. Qualifications: Basic Qualifications: Position requires a minimum 4-year degree in Chemistry, Biochemistry, Molecular Biology, Biology or related field; advanced degree helpful. Must have a minimum of 6-8 years experience in Regulatory Affairs or equivalent experience within the pharmaceutical industry. Previous experience in leading submission teams for marketing application and/or clinical trial applications and direct experience in interacting with regulatory authorities is also required. Preferred Qualifications: Must demonstrate a solid working knowledge of drug development process and knowledge of FDA regulatory requirements; EU, Canada, and ROW experience highly desirable. Candidates must be able demonstrate strong project management, problem-solving, negotiating, interpersonal and communication skills (both written and oral). Want to learn more about us? ... Read more »
Associate Director, Regulatory Affairs
2012-02-07 10:19:17
Company Information: At Millennium: The Takeda Oncology Company; "We Aspire to Cure Cancer". Millennium is a leading biopharmaceutical company focused on oncology that combines the agility, ideals and camaraderie of a start-up with the resources of Japan's largest pharmaceutical company. The result is a creative, entrepreneurial environment where quality science and making a difference in patients' lives are the priorities. Here, employees who share a drive and commitment to innovation for the benefit of oncology patients find their ideas, experience and contributions are valued and rewarded. Millennium offers great benefits, a friendly and respectful atmosphere, and a culture that promotes flexibility between work and life and encourages employees to give back to their community. Position Summary: This Associate Director position is established to play a key role in the planning and management of regulatory submissions to global health authorities. This individual is expected to provide leadership within Regulatory Affairs and all other data-generating departments to ensure timely filing and approval of assigned oncology programs. Duties and Responsibilities: Direct management of assigned oncology programs; driving all submission activities (IND/CTA, trial maintenance, NDA/BLA) and health authority interactions (meeting requests and briefing documents); represent Regulatory Affairs at various project team and working group meetings; assess and communicate regulatory requirements to ensure all development activities are in compliance with applicable regulations and guidelines; contribute significantly to the development of regulatory strategy plans; liaise with partnering companies to ensure regulatory alliance; act as direct point of contact with FDA and other regulatory authorities for general issues; mentor and coach junior regulatory staff and other team members. Qualifications: BASIC QUALIFICATIONS: A BS degree in a scientific or technical discipline plus a minimum of 6-8 years experience in Regulatory Affairs is required. Previous experience in leading submission teams for marketing application and/or clinical trial applications is also required. Must demonstrate a solid working knowledge of drug development process and knowledge of FDA regulatory requirements. Direct experience in interacting with regulatory authorities; Candidates must be able to influence others and demonstrate strong project management, problem-solving, negotiating, interpersonal and communication skills (both written and oral). PREFERRED QUALIFICATIONS: Knowledge of EU, Canada, ROW and post-marketing and experience interacting with DDMAC is a plus. Advanced degree preferred. Want to learn more about us? ... Read more »
Director of Compliance Auditing and Monitoring
2012-02-07 10:19:17
Company Information: At Millennium: The Takeda Oncology Company; "We Aspire to Cure Cancer". Millennium is a leading biopharmaceutical company focused on oncology that combines the agility, ideals and camaraderie of a start-up with the resources of Japan's largest pharmaceutical company. The result is a creative, entrepreneurial environment where quality science and making a difference in patients' lives are the priorities. Here, employees who share a drive and commitment to innovation for the benefit of oncology patients find their ideas, experience and contributions are valued and rewarded. Millennium offers great benefits, a friendly and respectful atmosphere, and a culture that promotes flexibility between work and life and encourages employees to give back to their community. Position Summary: We currently have a dynamic compliance position, reporting to the Chief Compliance Officer in a company with a growing oncology presence. This position's primary responsibility will be to continue to develop and implement a comprehensive compliance auditing and monitoring program to address both PhRMA Code obligations and other legal requirements such as FCPA. The ideal candidate will enjoy building an auditing and monitoring program, developing individuals in the auditing/monitoring role and supporting the business in appropriately reaching its goals. The ideal candidate will be business oriented and enjoy working closely with the business units collaboratively. The Director will provide comprehensive planning and guidance for the implementation and administration of the auditing and monitoring program. Duties and Responsibilities: Conduct complex Ethics & Compliance annual audit and monitoring plan activities based on risk assessments, results of current and prior audit and monitoring activities, outcomes from investigation process, and other relevant sources. - Manage change via effective communication with stakeholders related to the conduct of audit and monitoring activities. - Collaborate across the organization with key functional areas for the identification of issues that may require inclusion in audit and monitoring activities, as well as to ensure maintenance of agreed upon processes and timely, effective implementation of any new deliverables based on the outcome of audit and monitoring. - Demonstrate competency in organizing and evaluating facts and evidence to draw sound conclusions in relation to focused audit work or monitoring of organizational activities and processes. 5. Prepare timely, accurate, and complete reports with corrective action recommendations and follow-through with key stakeholders for implementation. 6. In concert with the Chief Compliance Officer, develop, implement and coordinate audit and monitoring with corrective action protocols for detected problems/violations. 8. Locate and analyze relevant data which may be obtained from the conduct of interviews, ride-alongs and program attendance, physical documentary evidence, files, and official records. Qualifications: The ideal candidate will have at least 5-10 years audit experience and at least 3 years experience implementing and developing compliance auditing programs for pharmaceutical companies. Knowledge of audit techniques including risk analysis identification skills is required. In addition, solid knowledge of Federal health care regulations, FDA and OIG laws/guidelines in relation to compliance program administration within the pharmaceutical industry is a must. The candidate must have the proven ability to evaluate trends, organize and conduct multiple, simultaneous audit and monitoring initiatives, deal tactfully with others, prepare accurate and sound reports, and coordinate with many cross-functional stakeholders to achieve identified outcomes. The ideal candidate also will have strong interpersonal, communication, and presentation skills. This position requires political savvy and the ability to take difficult or unpopular positions when necessary to protect the company. Want to learn more about us? ... Read more »
Product Manager/Sr. Product Manager, VELCADE Network Marketing
2012-02-07 10:19:17
Company Information: At Millennium: The Takeda Oncology Company; "We Aspire to Cure Cancer". Millennium is a leading biopharmaceutical company focused on oncology that combines the agility, ideals and camaraderie of a start-up with the resources of Japan's largest pharmaceutical company. The result is a creative, entrepreneurial environment where quality science and making a difference in patients' lives are the priorities. Here, employees who share a drive and commitment to innovation for the benefit of oncology patients find their ideas, experience and contributions are valued and rewarded. Millennium offers great benefits, a friendly and respectful atmosphere, and a culture that promotes flexibility between work and life and encourages employees to give back to their community. Position Summary: This individual will be responsible to support short and long-term marketing strategies, programs and tactics associated with the marketing of VELCADE in the US, specifically with the large Oncology Networks. The individual will report to the Director, Oncology Network and Payer Marketing. This person will work closely with a multitude of functional groups, including but not limited to VELCADE Marketing, US Market Access, the Oncology Networks team, Sales, Regulatory, Market Research, Commercial Operations, Legal and Global Medical Affairs. Duties and Responsibilities: Responsibilities include: .Lead execution of marketing strategies and the development of programs and tactics to attain strategic objectives associated with VELCADE in targeted customer segments. .Develop tools and programs for multiple audiences, including but not limited to HCPs in Oncology Networks, Nurse Navigators, and practice management professionals. .Coordinate planning and development of content for key oncology network congresses. .Lead the content development and meeting executiion of advisory boards. .Be a member of the VELCADE brand team. .Cultivate and maintain relationships with internal partners, thought leaders, customers and professional organizations. .Manage promotional budgets, and develop metrics to measure ROIs and ensure a cost effective allocation of resources. .Work successfully with all vendores/agencies. .Demonstrate compnay values on a consistent basis. Acts, and is accountable to act, in compliance with all laws, regulations and policies. .Performs other duties as requested. Qualifications: Basic Qualifications: .Bachelor's degree in business, finance or life sciences and 5+ years relevant experience in pharmaceutical marketing and/or reimbusement (or equivalent combination of education and experience) required .Successful track record in pharmaceutical marketing, reimbursement and/or sales with 5+ years relevant experience with increasing job responsibilities .Candidates must possess the ability to proactively identify and analyze business issues, develop solutions, implement tactical programs and design metrics to measure business impact .Prior experience managing marketing/advertising/promotion budgets .Demonstrated ability to effectively communicate, influence and lead .Individual must possess the ability to build consensus in a matrix enviornment with multiple functional groups supporting the brand team .Evidence of good analytical skills, project planning and organizational skills required .Experience working with cross-functional groups made up of one or more of the following: Marketing, Reimbursement, Sales, Global Medical Affairs, Market Research or Finance .Excellent communications and vendor/agency managment skills Preferred Qualifications: .Scientific Degree, MBA or other advanced degree is a plus .Experience working in Oncology therapeutic area - oncology reimbursement or marketing are strongly preferred Want to learn more about us? ... Read more »