http://bauschandlomb.jobs2web.com/go/New-Jersey-Healthcare-Jobs/118200/ View New Jersey Healthcare Jobs at Bausch and Lomb en-us http://basf.jobs2web.com/images/bauschandlomb/logo.gif http://bauschandlomb.jobs2web.com/go/New-Jersey-Healthcare-Jobs/118200/ 720 Job Title:
Sr. Brand Manager, Global OTC Pharmaceutical Marketing

Req #:
5116BR

Job Description:
PURPOSE: Lead the development of robust category level strategies for key global OTC pharmaceutical brands and therapeutic areas within Ophthalmology. Collaborates closely with the Regional teams, R&D Project Management, Regulatory and Medical to ensure successful global launches, in-market performance and life cycle management of key global brands. Develops brand plans and supports Regional implementation. RELATIONSHIPS: Reports to the Global Head of OTC Marketing within the Pharmaceuticals Business Unit. Leads the Global brands team and the extended cross-functional team. Interacts extensively with all areas of the business - particularly Regional Marketing and Sales, R&D Project Management, Regulatory, Medical and Business Development. ESSENTIAL FUNCTIONS: BRAND AND THERAPEUTIC AREA STRATEGY: Leads Global brand team and extended cross-functional team to ensure successful global launches, in-market performance and life cycle management of key prescription pharmaceutical brands. Defines robust therapeutic area strategy to strengthen the in-market and pipeline portfolio in close collaboration with the R&D, Business Development and Regional Marketing and Sales. Develops Global brand plans to maximize key pipeline and in-market brands, including global launch plans, positioning, branding, life cycle management and forecasting. Supports Regional implementation of brand plans and sharing best practices to ensure excellent in-market execution. Partners with Marketing Intelligence to generate insights on customer needs, competitive dynamics and brand positioning / performance and incorporate these into strategies / plans. Ensures excellent matrix management and develops strong relationships with key internal and external stakeholders. Participates in cross-functional projects and select business development opportunities. BUDGET: Oversees the global brand budget and ensures that resources are appropriately allocated and high quality deliverables are produced. DEVELOPMENT OF PEOPLE: Supports Regional / local brand managers and helps to build capabilities within the Global brand and cross-functional teams; develops clear brand / team KPIs. Manage the application and communication of all B&L policies and procedures.

Qualifications
KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS: Bachelors Degree required. Masters degree preferred. 6 - 10 years relevant OTC Pharmaceutical marketing experience, demonstrating a steady career progression with increasing roles of responsibility. Prior experience launching a OTC Pharmaceutical product required. Prior experience in Global Marketing or in Marketing in more than one Region strongly preferred. Sales experience preferred. Strong analytical and quantitative analysis skills required. Strong influencing, cross-functional collaboration and customer service skills required. Ability to plan, organize, and deploy resources according to urgency/importance. Presentation/communications skills must be excellent. Strong Innovation and Adaptability: must be able to identify better ways of doing things and getting others excited about new approaches. OTHER: Works within B&L's established policies and procedures. Embraces B&L Values in spirit and actions. Up to 25% overnight travel.

Work Location NJ-Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Sr_-Brand-Manager,-Global-OTC-Pharmaceutical-Marketing-Job-NJ-07940/514695/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Sr_-Brand-Manager,-Global-OTC-Pharmaceutical-Marketing-Job-NJ-07940/514695/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Drug Development Project Manager - Pharmaceuticals

Req #:
5369BR

Job Description:
Reporting to the Director, Pharmaceutical Project Management, the Project Manager will use the global PDP (Product Development Process), allied systems & tools, to plan and manage/coordinate resources and activities related to cost improvement & product development projects throughout Global R&D, and other B&L organizations.

Job Duties:
- Champion and lead projects for new product, cost improvement, and product improvement projects. - Management of projects in compliance with PDP process and procedures. - Management of project team members from the various other functional areas assigned to a specific program (includes team meetings, communications to teams and meeting minutes etc.). - Along with project team, lead the development and implementation of a project plan, schedule, budget and capital plan as required. - Review and monitor program/project activities against definition, schedule and costs. - Prepare amended budget forecasts as required. - Deliver products to agreed timelines and budgets. - Communicate effectively with RD&E management and staff regarding the

Status of all activities. - Inform management in a timely manner of any problems which may result in a delay in project schedules so that appropriate action may be taken. - Publish monthly/quarterly project report summaries as required. - Product presentations to development committee and senior management.

Qualifications
- Bachelors degree in science required with 10+ years of related experience. - 5 - 7 years pharmaceutical drug development project/program management experience with specific experience in managing complex, highly technical R&D/Drug Development related activities. Global experience a plus. - Prior training in project management. PMI certification a plus. - Proven, hands-on, results-oriented manager with demonstrated leadership skills across functional lines and a participatory style of working effectively in a dynamic, team-oriented environment. - Ability to communicate and interact at all levels from senior management to staff level. - Ability to translate customer requirements into measurable design goals/input. - Competency in Microsoft Project, Word, PowerPoint & Excel. - Excellent verbal, written and electronic communication skills. - Therapeutic area experience in ophthalmology, anti-infective or anti-inflammatory is preferred. - Proficiency in a foreign language (German, French) a plus.

Work Location NJ - Madison Relocation Available Yes Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Drug-Development-Project-Manager-Pharmaceuticals-Job-NJ-07940/671369/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Drug-Development-Project-Manager-Pharmaceuticals-Job-NJ-07940/671369/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Regulatory Affairs Senior Specialist - OTC/Nutritionals

Req #:
5305BR

Job Description:
Position Summary The Global Regulatory Affairs Senior Specialist handles activity for developing pharmaceutical regulatory strategies, submissions, and managing interactions with the regulatory agencies for OTC/Nutritional products. Specific Job Duties ? Provide support for the execution of the global product regulatory strategy for OTC/Nutritional pharmaceutical products ? Support regulatory aspects of product development team for agency filing ? Work with Regulatory Affairs Senior Manager for OTC/Nutritionals to make certain all product documentation is developed in accordance with regulatory requirements; serve as designee as needed ? Support the preparation of documentation and materials required for meetings with Regulatory Affairs for assigned products ? Liaise with country specific Regulatory Affairs personnel for international submissions and registrations ? Work with Labeling Senior Manager to make certain that all labels and labeling are accurate Technical Competencies ? Knowledge of pharmaceutical industry regulatory affairs discipline throughout the product lifecycle, including Development, Promotion and Advertising, Labeling, CMC, Commercialization, and Operations ? Knowledge of domestic and international regulations laws, regulations, and guidance ? Knowledge of clinical development, including responsibilities for successful management of development milestones and global market authorization ? Ability to partner with cross-functional teams in a global pharmaceutical organization ? Ability to understand scientific information and assess whether technical arguments are articulated clearly ? Ability to assess project risks and where appropriate, escalate accordingly Professional Competencies ? Demonstrated ability in analytical reasoning and critical thinking skills ? Strong capability to contribute to a team environment ? Strong business acumen and ability to see the business drivers outside of Regulatory Affairs ? Excellent communication skills; both oral and written ? Strong interpersonal skills with the ability to influence others in a positive and effective manner ? Demonstrated ability to contribute to a continuous learning and process improvement environment ? Capacity to react quickly and decisively in unexpected situations ? Detail-oriented with the ability to proofread and check documents for accuracy and inconsistencies ? Focused ability to influence operational excellence and performance metrics ? Risk adverse where needed with the ability to identify potential solutions to complex problems

Qualifications
? 5+ years relevant pharmaceutical industry and regulatory experience (or 2+ years pharmaceutical experience with a masters in Regulatory Affairs) ? OTC/ Nutritional experience highly preferred ? Bachelors degree in science or health related field ? Advanced degree preferred (PhD, MD, MS, PharmD, or equivalent)

Work Location NJ - Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Regulatory-Affairs-Senior-Specialist-OTC-Nutritionals-Job-NJ-07940/641700/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Regulatory-Affairs-Senior-Specialist-OTC-Nutritionals-Job-NJ-07940/641700/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Head of Clinical & Scientific Affairs

Req #:
5367BR

Job Description:
Position Summary: The Head of Pharmaceutical Clinical & Scientific Affairs at Bausch & Lomb is responsible for the development of products in the Rx, OTC, Generics, and Nutraceuticals categories. Leads a group of scientists (MDs and ODs) responsible for clinical trial design, scientific evaluations during the conduct of the trials (monitoring of safety, eligibility, enrollment, and data consistency), and analysis of results.

Job Duties:
* Accountable for product clinical development programs that are of high-quality, but that also lead to timely and cost-effective regulatory approval. * Serves as the leader of the Pharmaceutical Global Clinical Development matrixed team in the planning and executions of clinical trials. The team includes operations, statistics, data management, and medical writing, in addition to scientists. * Collaborates and takes clinical leadership role within cross-functional teams, including project managers, preclinical, regulatory, clinical trial materials, etc. * Responsible for the clinical aspects of clinical study reports and responses to regulatory authorities. * Contributes to abstract/manuscript/presentation writing/review, for scientific meetings and internal management reviews. * Maintains responsibility for the clinical input into Business Development due diligences. * Provides medical expertise and medical evaluation of questions regarding ophthalmology clinical practice. * Develops/Maintains relationships with external experts who might be needed to support clinical development programs. * Provides scientific and clinical research expertise in the development of overall strategy of the Pharmaceutical business and more specific product clinical development plan. * Performs management functions as goal setting, individual development plans and performance evaluations of staff. Identifies training needs to staff and implements training plan. * Proactively evaluates and contributes to process improvement.

Qualifications
Qualifications: * MD required - Ophthalmology experience strongly preferred. * Experience: Minimum 7-10 years research, clinical trial, or related experience. Must have excellent communication, organizational, and writing skills. *

Special Skills:
Experience with ophthalmic pharmaceuticals for the treatment of glaucoma and dry eye preferred.

Work Location NJ - Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Head-of-Clinical-&-Scientific-Affairs-Job-NJ-07940/669167/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Head-of-Clinical-&-Scientific-Affairs-Job-NJ-07940/669167/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Associate Director, Clinical Affairs

Req #:
5368BR

Job Description:
Position Summary: Participate in pharmaceutical project development teams and facilitate regional and global clinical development. Accountable for expert ophthalmic contributions including the identification and evaluation of clinical scientific issues related to clinical trial implementation. Interpret clinical data and contribute to clinical study reports and related documentation required for pharmaceutical clinical development. Specific

Job Duties:
. Participate on pharmaceutical R&D teams as a clinical scientific representative. . Provide scientific expertise for pharmaceutical clinical development with respect to the planning and execution of clinical trials, including cross-functional collaboration and communication and global clinical scientific representation. . Provide input and oversight for all clinical scientific aspects of registrational trials including safety, tolerability and efficacy reporting. . Participate in global clinical development meetings, contribute to harmonized protocol designs, participate in and present clinical data during internal and external meetings and symposia. . Develop and maintain strong scientific relationships with medical experts in support of clinical development programs. . Manage all clinical scientific aspects of pharmaceutical clinical trials. . Ensure compliance with FDA regulations, GCP and ICH guidelines. . Identify and evaluate clinical scientific issues related to projects and implementation of sound resolutions. . Provide input on R&D departmental decisions related to processes and procedures.

Qualifications
Qualifications: .

Education:
MD or PhD required (MD, Ophthalmology preferred) . Experience: Minimum 5 years research, clinical trial or related experience. Must have excellent communication, organizational, and writing skills. .

Special Skills:
Experience with ophthalmic pharmaceuticals for the treatment of glaucoma and dry eye preferred. Demonstrated ability to train study personnel and study CRAs. Ability to manage multiple projects simultaneously. . Specialized Training: Experience/training in GCP, ICH, and/or FDA pharmaceutical regulations is beneficial.

Work Location NJ - Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Associate-Director,-Clinical-Affairs-Job-NJ-07940/669168/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Associate-Director,-Clinical-Affairs-Job-NJ-07940/669168/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS