better Director Legal Affairs Job

Job Advertised by Pharmadiversity Job Board - OBJECTIVES: Provides regulatory strategic direction for the global development and implementation of regulatory activities for one or more projects. Responsible for multi-disciplinary or multi-faceted development programs (i.e. multiple indications for a given compound). Supervises trains and provides technical and regulatory guidance to staff. Provides regulatory therapeutic area strategic guidance on development projects and marketed products

Position: Director of Regulatory Compliance/Quality Assurance Location: Dallas / Ft. Worth area Salary: $110,000 to $140,000 + up to 20% bonus Reports to: VP, Corporate Quality and Regulatory Affairs Relocation: yes ABOUT THE COMPANY This company is a world-wide market leader in strong and growing markets in over 60 countries around the world. Today it is a leading supplier of medical

SUMMARY: Directly responsible for the organization and preparation of IND/CTA submissions. Coordinates the activities required to maintain the IND/CTA filings in Regulatory Compliance. Participates in compliance activities including SOP creation/revision and departmental training exercises. RESPONSIBILITIES: - Direct the preparation (content) of submissions (INDs, IND amendments, CTAs, CTA amendments, BLAs and BLA supplements and periodic reports) to the Health Agencies. Responsible for coordination

Job Description: Alcon, Inc. is the world's leading eye care company with sales of $5.6 billion in 2007. The company's nearly 15,000 employees worldwide, work in 75 facilities around the world to research, develop, manufacture and sell eye care products in more than 180 countries. Alcon is the largest specialty eye care company in the world and leads the growing $14.5 billion market for eye care products. Alcon has delivered strong and stable growth for over 60 years, and it is positioned to build on this record

Director, Regulatory Affairs Requisition ID 27234 Full/Part Time Location San Jose, CA Description General Summary: Responsible for a group of product lines, technology and specialized functions. Primary responsibilities include the identification, development, and implementation of strategic initiatives, franchise structure, and management development. SPECIFIC DUTIES AND RESPONSIBILITIES: . Establish and support a work environment of continuous improvement that supports BSC's Quality Policy, Quality System

Director of Regulatory Affairs - BSC Requisition ID 22973 Full/Part Time Location Valencia, CA Description Manage the regulatory affairs function. Generate or direct regulatory affairs specialists in the preparation of submissions to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Provide leadership and direct activities to ensure compliance with worldwide regulatory requirements. DUTIES: 1. Generate or direct regulatory affairs specialists

Associate Director, Regulatory Affairs Our Client is a world leader in eye care products. They have 75 facilities worldwide. They are expanding their RA organization and are in need of a quality regulatory professional Responsibilities: - Support the registration and approval of Surgical Instrumentation in selected global markets (Key US, EEA, Australia, Canada, Japan and ROW markets

Associate Director, Regulatory Affairs Our Client is a world leader in eye care products. They have 75 facilities worldwide. They are expanding their RA organization and are in need of a quality regulatory professional Responsibilities: - Support the registration and approval of Surgical Instrumentation in selected global markets (Key US, EEA, Australia, Canada, Japan and ROW markets

Associate Director, Regulatory Affairs Our Client is a world leader in eye care products. They have 75 facilities worldwide. They are expanding their RA organization and are in need of a quality regulatory professional Responsibilities: - Support the registration and approval of Surgical Instrumentation in selected global markets (Key US, EEA, Australia, Canada, Japan and ROW markets

Associate Director, Regulatory Affairs Our Client is a world leader in eye care products. They have 75 facilities worldwide. They are expanding their RA organization and are in need of a quality regulatory professional Responsibilities: - Support the registration and approval of Surgical Instrumentation in selected global markets (Key US, EEA, Australia, Canada, Japan and ROW markets

Associate Director, Regulatory Affairs Our Client is a world leader in eye care products. They have 75 facilities worldwide. They are expanding their RA organization and are in need of a quality regulatory professional Responsibilities: - Support the registration and approval of Surgical Instrumentation in selected global markets (Key US, EEA, Australia, Canada, Japan and ROW markets

Associate Director, Regulatory Affairs Our Client is a world leader in eye care products. They have 75 facilities worldwide. They are expanding their RA organization and are in need of a quality regulatory professional Responsibilities: - Support the registration and approval of Surgical Instrumentation in selected global markets (Key US, EEA, Australia, Canada, Japan and ROW markets

POSITION SUMMARY: Position will be responsible for overseeing and coordinating Pharmacy/Part D compliance activities, including preparations for regulatory audits, coordination of communications materials requiring CMS approval, annual preparation of Evidence of Coverage (EOC), coordinating follow-up on CMS guidance, periodic Medicare Part D reporting, and other internal audit activities. Position will serve as the Pharmacy department s liaison with the Compliance Department, including serving as a member

POSITION SUMMARY: Position will be responsible for overseeing and coordinating Pharmacy/Part D compliance activities, including preparations for regulatory audits, coordination of communications materials requiring CMS approval, annual preparation of Evidence of Coverage (EOC), coordinating follow-up on CMS guidance, periodic Medicare Part D reporting, and other internal audit activities. Position will serve as the Pharmacy department s liaison with the Compliance Department, including serving as a member

Associate Director, Regulatory Affairs Req. Code : Reg108 Location : Wilmington NC US 28405 Travel Required : None Job Type : Full Time Career Level : Manager (Manager/Supervisor of Staff) Education : Bachelor's Degree Category : Quality/Regulatory Job Description : AAIPharma is a leading international provider of pharmaceutical and biotechnology product development services. Our employees work in state-of-the-art facilities using leading edge technologies to meet exciting drug development challenges. We are

Job Advertised by Pharmadiversity Job Board - New Cancer Center in need of a Director of Compliance. A new position desire 3 years clinical experience prefer oncology or intensive care 5 years experience in compliance setting know coding in relation to billing process experience with CDM maintenance and review know revenue cycle management knowledge of IS and interfaces solid communication and interpersonal skils. Salary range $90100K + bonus depending on qualifications and experience. If you are interested

Director- Risk & Compliance Back Date Posted: 4/20/2005 Location: Quincy, Massachusetts Division Wealth Manager Services Position #: HNW05068 Job Type: Full Time Description -Provides management and direction for compliance and risk function of Wealth Manager Services. Works with WMS Senior Management to maintain and enhance a comprehensive compliance and risk management program for WMS' two product lines, Private Client Services and Managed Accounts. Through the Risk Management Self Assessment process

Job ID: 10622 Posting Title: Director, Compliance Work Location: Regular/Part-Time: Full-Time Regular Required Relevant Experience: 7 years Education Required: Bachelors Degree Travel Required: Job Description: Take Care Health Systems, one of the largest managers of convenient care clinics, is a wholly-owned subsidiary of Walgreens, the nation ??s largest drugstore chain. Convenient care clinics managed by Take Care Health Systems provide high-quality, convenient, and affordable health care to all individuals

Director - Regulatory Programs Location: Seattle, WA Last Updated: 10/08/2008 Job Description: Director - Regulatory Compliance Virginia Mason Medical Center Seattle, WA Full Time Competitive Salary Known for innovations in patient care, Virginia Mason Medical Center is a regional referral, teaching and research center. Our vision to be the Quality Leader in healthcare is achieved by adopting best practices as standard work and by improving systems via the Virginia Mason Production System, which uses Lean

Earn an opportunity to work as the new Director of Regulatory Affairs with an established, growing, and financially sound biopharmaceutical company in the greater Boston area. Job Description - Guide the writing, reviewing and submission of documentation for local, state, federal and international laws in support of early and late phase studies. - Act as the direct liaison with FDA and other health authorities to promote the timely review and approval of applications. - Assess regulatory requirements

management customs brokers freight forwarders internal external legal counsel customers suppliers and government officials...maximize opportunities including but not limited to legal Tax Supply Chain Supply Base HS E...

This position is open as of 11/10/2008. Sr. Director, Regulatory Affairs - Diagnostic Medical Devices - Tucson Sr. Director, Regulatory Affairs - Diagnostic Medical Devices - Tucson We are one of the world's leading developers and manufacturers of medical diagnostic instrument and reagent systems. Our products are found in laboratories of some of the world's largest pharmaceutical and biotechnology companies, government labs, and medical research centers. We are a global organization providing healthcare

all minimum qualifications except when there are legal requirements such as a license certification registration...

This position requires discussion and handling of highly sensitive and or confidential issues with significant legal implications...developments by maintaining broad based awareness of legal regulatory administrative judicial and current events research...

Director, Regulatory Affairs for i3 Research - Cary, NC 217810 Job Description Submit Description i3 Research is a full-service contract research organization (CRO) focused on four CORE areas: central nervous system; oncology; respiratory and infectious disease; and, endocrinology and metabolic disease. Therapeutic specialization drives all aspects of business in this global CRO from project staffing and talent management to quality initiatives, such as six sigma. As a UnitedHealth Group company,i3 Researchis

Conduct state specific legal research and monitor changes to requirements to mitigate risks and achieve compliance...

Develop oversee and manage the legal and regulatory affairs responsibilities and matters in...Minimum of 5 years experience in a legal environment and or health care regulatory environment...

Minimum of 5 years experience in a legal environment and or health care regulatory environment...

Finance and Accounting Human Capital Information Technology Legal Affairs Public Affairs and Regulatory Affairs...

Dir Regulatory Affairs Company Siemens Healthcare Diagnostics Inc. Division SMSD - IVD OPS Functional Area QC - Quality Location NY - Tarrytown Req ID 72635 Job Type Regular Job Time Full-Time Experience Level Senior Level Required Education Bachelors Degree Required Travel 20% Company Description Siemens Healthcare Diagnostics Inc. offers a broad portfolio of performance-driven diagnostic solutions that provide more effective and efficient ways to anticipate, diagnose, monitor and treat disease. Our products

as required Prepare and or review legal opinions legal research and analytical...Director of Legal Affairs D 1 DEADLINE FOR APPLICATIONS Open...such documents as they may pertain to legal matters Provide substantive expertise to meetings involving...

Ethics Brand Business Support Center Functional Area Legal State Tennessee Job Description Position Summary This...the ServiceMaster conducting high level investigations performing legal research assessing future risks and evaluating the...

Ph D in a scientific field or legal is strongly preferred bull A minimum of...

Pharmaceutical Sciences within PGRD together with Manufacturing Legal Worldwide Medical and Marketing to ensure alignment...

Director of Regulatory Strategy Job ID: 15683slg Location: St. Louis, MO Industry: Biotech Job Type: full-time Description: Director of Regulatory Strategy Location:St. Louis, MO Posting Number: 15683 Job Title: Director of Regulatory Strategy Location: St. Louis, MO Willing to Relocate: Yes Compensation: $110k-$125k Education Requirements: BS required, MS/PhD Preferred Chance to join growing, well established CRO! Information Contact Information The SearchLogix Group Contact Reply Form Forward to a

Job Title : Dir Scientific & Regulatory Affairs Company : Schwan's Research and Development, Inc. Position Type : Full Time - Regular Exempt/Non Exempt : Exempt Shift : Not Applicable City : MARSHALL State : Minnesota Description : GENERAL PURPOSE This position is responsible for directing and managing the development and implementation of product labels in accordance to regulatory guidelines. The incumbent is also responsible for developing and directing programs or process to use regulatory guidelines to

Position Title Director Regulatory Affairs-Skincare/Footcare Business Division Global Specialty Operations - Consumer Healthcare Country U.S.A. Location NJ Roseland Job Description This position will manage Regulatory Strategy and lead a team of regulatory professionals to achieve regulatory goals and objectives in support of the Footcare and Skincare Healthcare Businesses globally. In this role, the successful candidate will provide guidance and advice to senior management to achieve goals related to regulatory

Position Title Associate Director, Global Regulatory Affairs Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description This is a global role with global responsibilities. HA interactions include, but are not limited to the US FD, EMEA, Japanese MHLW and other local country regulatory authorities. Since the incumbent is based in the U.S, he/she will also have direct liaison responsibility with the FDA for his/her assigned projects. Liaison activities with other regional or

Position Title Senior Director, Global Compliance & Business Practices Business Division Global Functions - Compliance Country U.S.A. Location NJ Kenilworth Job Description Reports to Vice President, Global Compliance & Business Practices and provides support to President, regional and country management teams for Animal Health. This position is responsible for the co-development and implementation of the Company’s Global Compliance function for Intervet/Animal Health through close interaction with

Position Title Director Regulatory Affairs International Business Division Global Specialty Operations - Consumer Healthcare Country U.S.A. Location NJ Roseland Job Description This position will develop regulatory strategy for international markets and lead a team of regulatory professionals to achieve regulatory goals and objectives in support of the HealthCare Products businesses internationally. In this role, the successful candidate will provide guidance and advice to senior management to achieve goals

Safety, Health & Environment / Compliance Regional Director Jun. 05, 2008 - May. 07, 2009 Location: Houston (greenspoint), TX Salary Range: DOE Exempt/Non-Exempt: Exempt Benefits: Company Car, Family Health and Dental, 401k w/matching, Profit Sharing, Etc. Type: Full Time Department: R&S- Gulf/Midwest Overhead Description: Major Purpose To manage, train, implement, and foster Savage?s Safety, Health and Environment (?SH&E?) goals and performance programs as directed by the respective Operating VP?s and support

Director, Regulatory Affairs Category: Regulatory/QA Description: POSITION SUMMARY: The incumbent is responsible for directing the activities, supervising and training the employees of the Regulatory Affairs Department. The incumbent represents Santarus as the primary spokesperson in front of drug regulatory agencies and is the senior regulatory official for the company. A primary responsibility is developing and carrying out product development strategies aimed at the most efficient regulatory approvals for

Job Advertised by Pharmadiversity Job Board - 13 years of record revenues - $600M FY08 Revenue - Join one of America s fastest growing specialty pharmaceutical companies! Reporting directly to the VP of Regulatory Affairs, the Senior Director of Regulatory Affairs will provide leadership and direction to a growing regulatory department that is filing a high volume of ANDA s, some of which are global in scope. In addition, the Senior Director will be responsible for the implementation of annual objectives

Director, Regulatory Affairs 126476 (NCI) Full Time Regular posted 8/25/2008 Job Category SCT - Scientist Req ID 126476 Able to obtain security clearance? None Currently possess security clearance? None Location Frederick, MD % Travel Relocation Yes Requirements Responsible for managing regulatory activities for the Regulatory Compliance and Human Subjects Protection Program (RCHSPP), including managing submission of regulatory documents to the FDA and other regulatory and NIH authorities

Royce North America Inc Area of Interest Legal Position Type Full Time Position Responsibilities...

Compliance Location IL Chicago Division Corporate Department Legal Compliance Description Responsibilities Supervising the Compliance Department...

Associate Director, Regulatory Affairs - Dublin 0805264 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly, with supporting medical

Chemicals Regulatory Director-NY Apply Online Job Description The PricewaterhouseCoopers (www.pwc.com/us) network of firms provides industry-focused assurance, tax and advisory services to build public trust and enhance value for its clients and their stakeholders. More than 146,000 people in 150 countries across our network share their thinking, experience and solutions to develop fresh perspectives and practical advice. As part of this global network, employees of PricewaterhouseCoopers LLP ("PwC") have

Determine and certify appropriate legal authority for exports and temporary imports of...

Associate Director, Regulatory Expert Requisition ID 1094 Full/Part Time Full-time Location Washington DC Description