<?xml version="1.0" encoding="UTF-8"?><rss version="0.92">
<channel>
	<title>Eagle Research</title>
	<link>http://www.eagleresearch.net</link>
	<description></description>
	<lastBuildDate>Wed, 22 Feb 2012 20:19:29 +0000</lastBuildDate>
	<docs>http://backend.userland.com/rss092</docs>
	<language>en</language>
	<!-- generator="WordPress/3.2.1" -->

	<item>
		<title>Manager/Sr. Manager &#8211; Regulatory Affairs &#8211; New Jersey</title>
		<description><![CDATA[This entry is part 21 of 21 in the series Job OfferingsPosition Report to:     Director, Regulatory Affairs Job Description: Assist in the review of pre-approval and post-approval submissions from internal team in accordance with current regulations from US FDA and Health Canada, as needed. Review includes a detailed scientific/regulatory review ensuring compliance to all [...]]]></description>
		<link>http://www.eagleresearch.net/2012/02/managersr-manager-regulatory-affairs-new-jersey/</link>
			</item>
	<item>
		<title>Senior Manager, Drug Safety &#8211; MASS</title>
		<description><![CDATA[This entry is part 20 of 21 in the series Job OfferingsPosition Overview: The Senior Manager, Drug Safety is responsible for managing a team of Safety Associates.  This includes development and implementation of processes necessary for day-to-day operations, as well as the appropriate monitoring of the safety of the company’s marketed products through pharmacovigilance activities [...]]]></description>
		<link>http://www.eagleresearch.net/2012/01/senior-manager-drug-safety-mass/</link>
			</item>
	<item>
		<title>Medical Director &#8211; Global Safety Officer &#8211; MASS or MN</title>
		<description><![CDATA[This entry is part 19 of 21 in the series Job OfferingsSummary: This key position within the Quality function is responsible for providing medical and scientific expertise to bring high quality and efficiency to promote patient safety for products worldwide. This position provides critical input to the clinical trials for devices in the product pipeline. [...]]]></description>
		<link>http://www.eagleresearch.net/2012/01/medical-director-global-safety-officer-mass-or-mn/</link>
			</item>
	<item>
		<title>Auditor/Senior Auditor &#8211; New York</title>
		<description><![CDATA[This entry is part 18 of 21 in the series Job OfferingsPosition Overview: R&#38;D compliance Assess quality systems, through audits and investigations of Contract Manufacturing Organization (CMOs), Contract Laboratories, raw material and component suppliers, clinical investigator sites, contract research organizations. Conduct on-site or paper audits and generates audit reports to qualify external supply organizations Maintain [...]]]></description>
		<link>http://www.eagleresearch.net/2012/01/auditorsenior-auditor-new-york-2/</link>
			</item>
	<item>
		<title>Recruiting Director &#8211; New Jersey</title>
		<description><![CDATA[This entry is part 17 of 21 in the series Job OfferingsRecruiting Director Unique opportunity to join the senior team of a well-established and well-regarded executive search firm that also offers expanded services. We want to speak with an experienced recruiter with a track record of success, who wants to spearhead the growth and manage [...]]]></description>
		<link>http://www.eagleresearch.net/2012/01/recruiting-director-new-jersey/</link>
			</item>
	<item>
		<title>Medical Writer, Phase I &#8211; Based in Maryland &#8211; position location flexible</title>
		<description><![CDATA[This entry is part 16 of 21 in the series Job OfferingsPosition Overview: The successful candidate will review and interpret clinical data, independently write, edit, compile and QC documents, ensure the accuracy and quality of applicable written deliverables, and ensure compliance with ethical, legal, scientific, regulatory and client standards. Role &#38; Responsibility: Review for quality [...]]]></description>
		<link>http://www.eagleresearch.net/2012/01/medical-writer-phase-i-based-in-maryland-position-location-flexible/</link>
			</item>
	<item>
		<title>Director, Post Marketing Regulatory Affairs &#8211; New Jersey</title>
		<description><![CDATA[This entry is part 15 of 21 in the series Job OfferingsDepartment: Medical and Regulatory Affairs Reports to: Sr. Vice President US Medical and Regulatory Affairs Position Summary: Oversight of regulatory activities supporting marketed products in US and Canada Supervising Associate Director of Quality Operations in the US Ensure efficient and compliant functioning of promotional [...]]]></description>
		<link>http://www.eagleresearch.net/2011/12/director-post-marketing-regulatory-affairs-new-jersey/</link>
			</item>
	<item>
		<title>Medical Director &#8211; Diabetes &#8211; New Jersey</title>
		<description><![CDATA[This entry is part 14 of 21 in the series Job OfferingsEssential Duties Overview: Provide endocrinology expertise to clinical trials in the drug and device development process Review and edit protocols to ensure accuracy, consistency with standard of care, logistical ease and internal consistency Develop, plan and implement clinical research direction and vision that are [...]]]></description>
		<link>http://www.eagleresearch.net/2011/12/medical-director-diabetes-new-jersey-2/</link>
			</item>
	<item>
		<title>Director, Regulatory Affairs &#8211; New Jersey</title>
		<description><![CDATA[This entry is part 13 of 21 in the series Job OfferingsReports to:     Vice President Global Regulatory Affairs Position Summary: The position will contribute to the development of product registration strategies for efficient Worldwide and US registrations. Primary responsibility is to ensure alignment of the registration plans with the commercial needs and to ensure regional [...]]]></description>
		<link>http://www.eagleresearch.net/2011/12/director-regulatory-affairs-endocrinology-new-jersey/</link>
			</item>
	<item>
		<title>Director, Drug Safety &#8211; New Jersey</title>
		<description><![CDATA[This entry is part 12 of 21 in the series Job OfferingsOverview: Responsible for providing drug safety management direction and vision in support of company objectives, goals and timelines Represent Drug Safety in development project teams and assume a key leadership role in providing clinical guidance for the drug safety area Key Responsibilities: Provide drug [...]]]></description>
		<link>http://www.eagleresearch.net/2011/11/director-drug-safety-new-jersey/</link>
			</item>
</channel>
</rss>

