http://bauschandlomb.jobs2web.com/go/Los-Angeles-Manager-Jobs/118217/ View Los Angeles Manager Jobs at Bausch and Lomb en-us http://basf.jobs2web.com/images/bauschandlomb/logo.gif http://bauschandlomb.jobs2web.com/go/Los-Angeles-Manager-Jobs/118217/ 720 Job Title:
Director, Clinical & Scientific Affairs

Req #:
5228BR

Job Description:
Position Summary The Surgical Director of Clinical & Scientific Affairs at Bausch & Lomb is responsible for the development of products in the Surgical medical device category. 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. Specific 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 Surgical 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 Surgical business and more specific product clinical development plan. . Performs management functions such 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. Management Competencies . Demonstrated knowledge and skill in submission strategies as well as overall Regulatory Science. . Demonstrated experience in leading a team and carrying out performance management and talent processes. . Ability to partner, negotiate, and drive towards win/win outcomes. . Develops effective global internal/external relationships (e.g. cross category, cross functional, etc.) . Excellent oral communication skills (command of English language) and technical writing skills. . Ability to effectively present information in one-on-one and small group situations to internal customers and other employees of the organization. Ability to communicate well with all levels of the organizations. Technical Competencies . Strong questioning and problem-solving skills. . Mathematical skills commensurate with educational background and necessary for describing and summarizing laboratory and/or clinical data in product registration submissions. . Ability to read, analyze and interpret governmental regulations, general business periodicals, professional journals and technical procedures. . Ability to write routine reports and business correspondence. . Computer literate with general office software and internet use.

Qualifications
. Medical Degree (MD / OD) from an accredited US or foreign medical school preferred. PhD with ophthalmic clinical study experience. . At least 5 years of total experience, post-medical training, including clinical practice AND industry experience in the planning, execution, and reporting of clinical trials. . Strong understanding of GCP, ICH, and regulatory compliance. . Knowledge of scientific methods, research design, and medical practices and procedures in ophthalmology.

Work Location CA - Aliso Viejo Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Director,-Clinical-&-Scientific-Affairs-Job-CA-92653/609162/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Director,-Clinical-&-Scientific-Affairs-Job-CA-92653/609162/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Director, Medical Affairs

Req #:
5224BR

Job Description:
Position provides leadership and management, within the Surgical business of medical and scientific, with support for approved products. Assists in the development of phase IV and Investigator Initiated Studies, peer to peer education of doctors, scientific publication and investigation of safety issues and business development. Acts as thought partner to marketing and R&D on designing Clinical Development Programs, labeling, and communications all within compliance parameters.

Job Duties:
- Takes an active role in managing Phase IV clinical programs supporting both products in development as well as marketed product globally. - Provides near and long-term strategic direction of the scientific platform and plays a major role in developing the research agenda for the Surgical business. - Develops and maintains relationships externally with advisory boards, professional associations, professional meetings and conferences, etc. to achieve business unit objectives. - Possesses ability to lead direct reports and oversee large-scale projects. Individuals in this position collaborate with internal stakeholders, external customers and key thought leaders to develop phase IIIb/IV research initiatives, and create clinical education and support programs. - Has knowledge of marketplace medical trends and works closely with the sales and marketing group to provide clinical input for marketing initiatives, sales materials, education and training. Industry specific knowledge medical & legal regulations, procedures, and practices that impact the business. - Strong ability to interpret and communicate clinical studies. Ability to recommend, present and defend appropriate product claims, scientific opinions and interpretations for products in prelaunch, launch and post launch phases. - Oversees scientific communication planning process, and coordinates closely with the medical education and CME groups. - Oversees the development and distribution of scientific and medical information to effectively provide accurate, quality, and up-to-date information to internal and external customers while meeting appropriate legal and regulatory requirements - Ability to forge strong external relationships with KOLs, PBMs, and the FDA and act as a liaison between company and clinical investigators. Develops credible relationships with opinion leaders, medical directors, and key regulatory officials. - Builds functional excellence by attracting and retaining top quality talent, maintaining strong external relationships, and maintaining strong internal lines to ensure appropriate flow of medical information. - Provides editorial content and comments for phase IV clinical study reports & manuscripts. Manages Phase IV Clinical Programs.

Qualifications
- MD/OD/PhD with Surgical/Ophthalmic experience - 7- 10 years in ophthalmic industry/medical device industry - Demonstrated experience with several products, led through clinical development, regulatory approval, and launch Management Competencies: - Demonstrated ability to collaborate with Commercial functions - Demonstrated ability to communicate and plan effectively with other departments and to respond to inquiries or complaints from customers. - Demonstrated ability to effectively present complex issues in oral and written form. - Participates in safety review committees and risk management activities as appropriate. - Demonstrated knowledge and skill in submission strategies as well as overall Regulatory Science. - Demonstrated experience in leading a team and carrying out performance management and talent processes. - Ability to partner, negotiate, and drive towards win/win outcomes. - Develops effective global internal/external relationships (e.g. cross category, cross functional, etc.) - Excellent oral communication skills (command of English language) and technical writing skills. - Ability to effectively present information in one-on-one and small group situations to internal customers and other employees of the organization. - Ability to communicate well with all levels of the organizations. Technical Competencies: - Strong questioning and problem-solving skills. - Mathematical skills commensurate with educational background and necessary for describing and summarizing laboratory and/or clinical data in product registration submissions. - Ability to read, analyze and interpret governmental regulations, general business periodicals, professional journals and technical procedures. Ability to write routine reports and business correspondence. - Computer literate with general office software and internet use.

Work Location CA - Aliso Viejo Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Director,-Medical-Affairs-Job-CA-92653/607603/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Director,-Medical-Affairs-Job-CA-92653/607603/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Accounting Manager

Req #:
5352BR

Job Description:
Position Summary The Manager of Accounting & Financial Reporting is responsible for accounting, financial reporting, and Sarbanes-Oxley compliance to support the Bausch & Lomb US Surgical commercial business. Specific Job Duties .Full responsibility for the finance accounting department of the US Surgical Division. .Manage and develop a team of four highly motivated finance accountants. .Improve financial and business processes by establishing standard operating procedures. .Coordinate monthly general ledger close to ensure accurate and timely reporting of monthly financial results under US GAAP and Sarbanes Oxley requirements. .Review journal entries; account analyses, corporate reporting submission, Sales & COGS, and Balance Sheet quarterly variance analysis. .Recommend accounting treatment of various transactions in accordance with US GAAP. .Maintain strong internal control documentation and controls, including periodic update of risk control matrix, flowcharts, narratives, and critical spreadsheets. .Act as the focal point for the audits and SOX testing and maintain communication with internal and external auditors. .Liaise with EPM and PeopleSoft support groups to resolve problems and improve processes.

Qualifications
Qualifications .Bachelor's degree in Accounting or Finance is required with 8+ years progressive experience with a minimum of 5 years experience in financial accounting and/or audit. .CPA preferred and/or experience working with public accounting or Sarbanes Oxley environments. .Advanced Peoplesoft, Excel and HFM experience a plus. .Taking initiative, positive attitude, flexibility and keen analytical skills are important attributes for this role.

Work Location CA - Aliso Viejo Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Accounting-Manager-Job-CA-92653/664782/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Accounting-Manager-Job-CA-92653/664782/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS