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Associate Director Director Compliance

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Company: Genzyme

Location: Cambridge, MA

Date Posted: June 8, 2014

Source: Genzyme

Associate Director/Director, Compliance-70065689-35258


Description

One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. Since its founding in 1981, the company has introduced breakthrough treatments that have provided new hope for patients. The company's areas of focus are rare genetic diseases, multiple sclerosis, cardiovascular disease and endocrinology. Genzyme is a Sanofi company. Genzyme's press releases and other company information are available at http://cts.businesswire.com...

Sanofi, a global and diversified healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, rare diseases, consumer healthcare, emerging markets and animal health. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).

Associate Director/Director, Compliance

Genzyme is currently seeking ...

Associate Director/Director, Compliance-70065689-35258


Description

One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. Since its founding in 1981, the company has introduced breakthrough treatments that have provided new hope for patients. The company's areas of focus are rare genetic diseases, multiple sclerosis, cardiovascular disease and endocrinology. Genzyme is a Sanofi company. Genzyme's press releases and other company information are available at http://cts.businesswire.com...

Sanofi, a global and diversified healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, rare diseases, consumer healthcare, emerging markets and animal health. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).

Associate Director/Director, Compliance

Genzyme is currently seeking a Compliance professional with industry experience to work with Genzyme’s Rare Disease and Multiple Sclerosis business units in the United States and Canada. This position is based in Cambridge, Massachusetts and level will be commensurate with the experience of identified candidate.

Key Responsibilities:

Help support the operation of Sanofi Group’s North America (NA) Compliance Program for Genzyme’s businesses in the United States and Canada, working under the direction of the Sanofi NA Compliance Officer and the Genzyme Global Compliance Officer

Cultivate an understanding of unique perspectives of internal partners and communicate clearly, concisely, and persuasively relevant Compliance requirements and how their needs are accommodated in the strategic and operational plan of the Sanofi NA Compliance Department

Understand the environment in which Genzyme operates and use analytical skills and experience to set Compliance priorities, make choices, and recommend options to minimize Compliance risk

Develop and leverage working relationships throughout Genzyme as well as the Sanofi NA Compliance Department to facilitate teamwork and achievement of mutual goals across organizational boundaries to achieve Compliance objectives

Support the effective implementation of NA Compliance policies, standards and procedures within Genzyme; work with members of Genzyme’s businesses to understand the policies, standards, and procedures and how to implement business initiatives within that context; identify and help close any Compliance gaps

Assess Compliance training needs for Genzyme’s businesses in light of external developments and risk areas and assist the Sanofi NA Compliance Department with the development and delivery of content to meet these needs

In coordination with the Legal Department and the Sanofi NA Compliance Department, assist with investigations relating to potential violations of NA policies, standards or procedures or other Compliance issues in all areas, including but not limited to fraud and abuse, product promotion and other regulatory matters, research and development, government price reporting and manufacturing

Assist with auditing and monitoring activities related to Genzyme’s businesses and help ensure compliance with applicable reporting requirements.

Support and implement policies, standards, and processes to meet commitments made by Genzyme to the federal government that may be included in settlements or other agreements, along with counseling Genzyme clients to comply with commitments made to the federal government

Assist in the implementation of reporting requirements and any additional commitments made by Genzyme to the federal government

Support operational efforts in connection with FMV, Transparency and training on standard operating procedures.

There will be some travel required with this position (less than 25%). The position does not have management or budgetary responsibilities.



Qualifications

Basic Qualifications:

BA/BS from an accredited school

5-7 years of experience with biotechnology, pharmaceuticals or human healthcare industries

Preferred Qualifications:

Advanced Degree preferred.

Substantive knowledge of applicable US laws relating to healthcare and life science business, plus familiarity with current the US life science marketplace

Working knowledge of US healthcare compliance considerations

Prior in-house experience preferred

Professional Skills:

Sound judgment and commitment to ethical conduct

Excellent communication, interpersonal and writing skills

Demonstrated ability to (i) understand and digest complex scenarios in order to identify relevant issues and risks, (ii) propose solutions that take into consideration the relevant business objectives, and (iii) communicate those issues, risks, and solutions clearly and concisely

Ability to work independently and to be reliable, responsible, responsive, and accountable

Team player with a commitment to developing strong collaborative relationships

Ability to organize, coordinate and motivate cross-functional teams

Ability to handle multiple responsibilities simultaneously and still meet high quality and timeliness standards under pressure

Strong attention to detail.

Relocation is available.

#LI-GZ



Job : Quality
Primary Location : United States-Massachusetts-Cambridge


Job Posting : Jul 30, 2014, 10:17:01 AM

Shift : Day Job
Job Type : Regular
Employee Status : Regular








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