Director, Corporate Counsel
Otsuka America Pharmaceutical Inc.
The Otsuka US Legal Team is looking for an attorney familiar with the legal and regulatory frameworks within which life sciences companies operate. The attorney will provide proactive guidance and counseling related to drafting, reviewing, and negotiating complex business transactions, including commercial supply agreements, manufacturing agreements, master services agreements, collaboration agreements, intellectual property license agreements, and acquisition agreements. This role offers the opportunity to provide legal advice in many different areas of corporate law, as well as direct legal support to several functional areas of our life sciences business, with an emphasis on technical operations, business development, and related regulatory quality matters.
The Director, Corporate Counsel will have experience in the pharmaceutical industry or at a law firm serving pharmaceutical industry clients and be able to bring a foundational understanding of the industry and the other functional areas within a pharmaceutical company. The candidate will have a strong background in contract law and negotiations, excellent analytical skills, and the ability to appropriately communicate complex legal concepts and potential risks clearly to non-legal stakeholders for consideration. As a Director within the Legal team, it is expected the individual will also work independently, be able to develop well-reasoned positions, and know when to appropriately escalate complex and unique topics for further discussion and consideration.
This role can be located in Otsuka’s Princeton, NJ or Rockville, MD offices, or it can be remote, but availability during US Eastern time zone business hours is mandatory. No matter where the role is located, up to 25% travel is required based upon business needs.
At Otsuka our mission is to create new products for better health worldwide. Our purpose is to defy limitation so others can too.
Otsuka is committed to diversity and inclusion in the workplace. Individuals seeking employment at Otsuka are considered without regards to race, color, religion, sex, sexual orientation, gender identification, national origin, age, marital status, ancestry, physical or mental disability, veteran status, or genetic information, among other protected bases.
To that end, the Legal Affairs department at Otsuka is seeking qualification as a Mansfield Rule 3.0 Certified Law Department as part of the Diversity Lab’s Mansfield Rule initiative, which measures and seeks to increase diversity within law departments. Providing your data during the application process helps us with achieving that goal and with meeting reporting/record-keeping obligations under federal and state law and other legal requirements. Providing your data is entirely voluntary and will not be considered in the hiring process or thereafter. Any information that you do provide will be treated confidentially.
**Job Description**
**Specific Role Responsibilities:**
+ Review, analyze, and negotiate agreements, such as commercial supply agreements, with suppliers and vendors to ensure alignment with company policies, risk management strategies, and regulatory requirements and processes;
+ Create, review, analyze, and negotiate strategic collaboration agreements, licensing agreements, acquisition agreements, or other agreements for business development transactions, ensuring they align with the company’s strategic goals and risk management strategies;
+ Provide internal clients in Technical Operations and Business Development, among others, with legal advice and guidance regarding terms and conditions of agreements and other related inquiries;
+ Draft and revise contract templates and related legal documentation to ensure clarity and enforceability;
+ Maintain current awareness of evolving FDA laws and regulations, as well as interpretations, advisory comments, enforcement actions and policy issues, especially as they relate to the business agreements being negotiated;
+ Collaborate with, counsel and coach colleagues in other functional areas as well as other attorneys and support staff working on complex transactions;
+ Provide guidance to multi-functional teams to ensure compliance with company policies and legal/regulatory requirements;
+ Work closely with other Corporate Counsel to administer policies, procedures, and guidelines in core compliance areas (e.g., anti-kickback, antitrust, anti-bribery, data privacy & security); and
+ Perform other legal, administrative and corporate duties upon request.
Ensure all licensing activities comply with relevant laws and regulations.
**Additional Director Responsibilities**
+ **Solutions Analysis** : Analyze specific problems and issues to find the best solutions. Solutions could be technical or professional in nature.
+ **Policies and Procedures Development:** Contribute to the drafting of policies, procedures, and related guidelines within an area of expertise to meet defined key principles and ensure compliance with external requirements.
+ **Internal Client Relationship Management:** Contribute to the management of partnering relationships with internal clients, building effective working relationships, and providing high-quality professional services to support in delivering business strategy and plans.
+ **Information and Business Advice:** Resolve queries from internal or external customers or suppliers by providing information on complex processes and the related policies, referring to others where necessary for interpretation of policy.
**Risk Scenario Modeling** : Analyze, assess, and quantify the risks associated with products/individual applications/business activities/the market to determine whether any risk is within the agreed risk appetite. Undertake tactical risk modeling.
**Qualifications**
**EDUCATION:**
+ Doctor of Jurisprudence (J.D.) or equivalent degree required
+ Admission to at least one state bar
**EXPERIENCE:**
+ Minimum of 5 years of relevant experience as an attorney in the pharmaceutical industry or at a law firm advising pharmaceutical industry clients
+ Experience & demonstrated ability to collaborate, build and sustain effective partnerships with multicultural key stakeholders and project teams
+ Strong negotiation (on paper and live person-to-person), drafting, and analytical skills
+ In-depth understanding or proven experience with respect to licensing practices
BEHAVIORAL COMPETENCIES
+ **Decision Quality:** Makes good and timely decisions that keep the organization moving forward.
+ **Ensures Accountability:** Holds self and others accountable to meet commitments.
+ **Communicates Effectively:** Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.
+ **Collaborates:** Builds partnerships and works collaboratively with others to meet shared objectives.
+ **Persuades:** Uses compelling arguments to gain the support and commitment of others. For example, states position with conviction and persuasive rationale.
+ **Develops Talent:** Develops people to meet both their career goals and the organization’s goals.
+ **Optimizes Work Processes:** Knows the most effective and efficient processes to get things done, with a focus on continuous improvement.
+ **Plans and Aligns:** Plans and prioritizes work to meet commitments aligned with organizational goals.
+ **Customer Focus:** Builds strong customer relationships and delivers customer-centric solutions.
+ **Business Insight:** Applies knowledge of business and the marketplace to advance the organization’s goals.
TECHNICAL COMPETENCIES
+ **Questions Strategically:** Works with limited guidance to uncover clients’ explicit needs and/or unforeseen opportunities and challenges.
+ **Analyze Alternatives and Recommend Solutions:** Works at an intermediate level to analyze potential solutions and create recommendations based on the expected benefits, costs, and overall value of the solution for key stakeholders.
+ **Policy and Regulation:** Works with limited guidance to interpret and apply knowledge of laws, regulations and policies in area of expertise.
+ **Effectively Presents Solutions:** Works with limited guidance to clearly present solutions that link directly to the key objectives and challenges important to the client.
+ **Project Risk and Issue Management:** Uses comprehensive knowledge and/or skills to act independently with guiding and training others on identifying, assessing, prioritizing and managing project related risks.
+ **Negotiation Support:** As necessary, collaborates with external legal counsel to ensure comprehensive support and expertise to draft and negotiate legally sound licensing agreement or other strategic business development agreements.
**Disclaimer**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to their protected veteran or disabled status, or any protected status
The Otsuka US Legal Team is looking for an attorney familiar with the legal and regulatory frameworks within which life sciences companies operate. The attorney will provide proactive guidance and counseling related to drafting, reviewing, and negotiating complex business transactions, including commercial supply agreements, manufacturing agreements, master services agreements, collaboration agreements, intellectual property license agreements, and acquisition agreements. This role offers the opportunity to provide legal advice in many different areas of corporate law, as well as direct legal support to several functional areas of our life sciences business, with an emphasis on technical operations, business development, and related regulatory quality matters.
The Director, Corporate Counsel will have experience in the pharmaceutical industry or at a law firm serving pharmaceutical industry clients and be able to bring a foundational understanding of the industry and the other functional areas within a pharmaceutical company. The candidate will have a strong background in contract law and negotiations, excellent analytical skills, and the ability to appropriately communicate complex legal concepts and potential risks clearly to non-legal stakeholders for consideration. As a Director within the Legal team, it is expected the individual will also work independently, be able to develop well-reasoned positions, and know when to appropriately escalate complex and unique topics for further discussion and consideration.
This role can be located in Otsuka’s Princeton, NJ or Rockville, MD offices, or it can be remote, but availability during US Eastern time zone business hours is mandatory. No matter where the role is located, up to 25% travel is required based upon business needs.
At Otsuka our mission is to create new products for better health worldwide. Our purpose is to defy limitation so others can too.
Otsuka is committed to diversity and inclusion in the workplace. Individuals seeking employment at Otsuka are considered without regards to race, color, religion, sex, sexual orientation, gender identification, national origin, age, marital status, ancestry, physical or mental disability, veteran status, or genetic information, among other protected bases.
To that end, the Legal Affairs department at Otsuka is seeking qualification as a Mansfield Rule 3.0 Certified Law Department as part of the Diversity Lab’s Mansfield Rule initiative, which measures and seeks to increase diversity within law departments. Providing your data during the application process helps us with achieving that goal and with meeting reporting/record-keeping obligations under federal and state law and other legal requirements. Providing your data is entirely voluntary and will not be considered in the hiring process or thereafter. Any information that you do provide will be treated confidentially.
**Job Description**
**Specific Role Responsibilities:**
+ Review, analyze, and negotiate agreements, such as commercial supply agreements, with suppliers and vendors to ensure alignment with company policies, risk management strategies, and regulatory requirements and processes;
+ Create, review, analyze, and negotiate strategic collaboration agreements, licensing agreements, acquisition agreements, or other agreements for business development transactions, ensuring they align with the company’s strategic goals and risk management strategies;
+ Provide internal clients in Technical Operations and Business Development, among others, with legal advice and guidance regarding terms and conditions of agreements and other related inquiries;
+ Draft and revise contract templates and related legal documentation to ensure clarity and enforceability;
+ Maintain current awareness of evolving FDA laws and regulations, as well as interpretations, advisory comments, enforcement actions and policy issues, especially as they relate to the business agreements being negotiated;
+ Collaborate with, counsel and coach colleagues in other functional areas as well as other attorneys and support staff working on complex transactions;
+ Provide guidance to multi-functional teams to ensure compliance with company policies and legal/regulatory requirements;
+ Work closely with other Corporate Counsel to administer policies, procedures, and guidelines in core compliance areas (e.g., anti-kickback, antitrust, anti-bribery, data privacy & security); and
+ Perform other legal, administrative and corporate duties upon request.
Ensure all licensing activities comply with relevant laws and regulations.
**Additional Director Responsibilities**
+ **Solutions Analysis** : Analyze specific problems and issues to find the best solutions. Solutions could be technical or professional in nature.
+ **Policies and Procedures Development:** Contribute to the drafting of policies, procedures, and related guidelines within an area of expertise to meet defined key principles and ensure compliance with external requirements.
+ **Internal Client Relationship Management:** Contribute to the management of partnering relationships with internal clients, building effective working relationships, and providing high-quality professional services to support in delivering business strategy and plans.
+ **Information and Business Advice:** Resolve queries from internal or external customers or suppliers by providing information on complex processes and the related policies, referring to others where necessary for interpretation of policy.
**Risk Scenario Modeling** : Analyze, assess, and quantify the risks associated with products/individual applications/business activities/the market to determine whether any risk is within the agreed risk appetite. Undertake tactical risk modeling.
**Qualifications**
**EDUCATION:**
+ Doctor of Jurisprudence (J.D.) or equivalent degree required
+ Admission to at least one state bar
**EXPERIENCE:**
+ Minimum of 5 years of relevant experience as an attorney in the pharmaceutical industry or at a law firm advising pharmaceutical industry clients
+ Experience & demonstrated ability to collaborate, build and sustain effective partnerships with multicultural key stakeholders and project teams
+ Strong negotiation (on paper and live person-to-person), drafting, and analytical skills
+ In-depth understanding or proven experience with respect to licensing practices
BEHAVIORAL COMPETENCIES
+ **Decision Quality:** Makes good and timely decisions that keep the organization moving forward.
+ **Ensures Accountability:** Holds self and others accountable to meet commitments.
+ **Communicates Effectively:** Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.
+ **Collaborates:** Builds partnerships and works collaboratively with others to meet shared objectives.
+ **Persuades:** Uses compelling arguments to gain the support and commitment of others. For example, states position with conviction and persuasive rationale.
+ **Develops Talent:** Develops people to meet both their career goals and the organization’s goals.
+ **Optimizes Work Processes:** Knows the most effective and efficient processes to get things done, with a focus on continuous improvement.
+ **Plans and Aligns:** Plans and prioritizes work to meet commitments aligned with organizational goals.
+ **Customer Focus:** Builds strong customer relationships and delivers customer-centric solutions.
+ **Business Insight:** Applies knowledge of business and the marketplace to advance the organization’s goals.
TECHNICAL COMPETENCIES
+ **Questions Strategically:** Works with limited guidance to uncover clients’ explicit needs and/or unforeseen opportunities and challenges.
+ **Analyze Alternatives and Recommend Solutions:** Works at an intermediate level to analyze potential solutions and create recommendations based on the expected benefits, costs, and overall value of the solution for key stakeholders.
+ **Policy and Regulation:** Works with limited guidance to interpret and apply knowledge of laws, regulations and policies in area of expertise.
+ **Effectively Presents Solutions:** Works with limited guidance to clearly present solutions that link directly to the key objectives and challenges important to the client.
+ **Project Risk and Issue Management:** Uses comprehensive knowledge and/or skills to act independently with guiding and training others on identifying, assessing, prioritizing and managing project related risks.
+ **Negotiation Support:** As necessary, collaborates with external legal counsel to ensure comprehensive support and expertise to draft and negotiate legally sound licensing agreement or other strategic business development agreements.
**Disclaimer**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to their protected veteran or disabled status, or any protected status
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $183,335.00 - Maximum $274,160.00, plus incentive opportunity: The range shown represents a typical pay range or starting salary for candidates hired to perform the work. Other elements may be used to determine actual salary such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. This information is provided to applicants in accordance with states and local laws.
**Company benefits** : Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; https://www.otsuka-us.com/careers-join-otsuka .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website https://vhr-otsuka.wd1.myworkdayjobs.com/en-US/External .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka’s call center at: 800-363-5670. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: https://www.ic3.gov , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. (“Otsuka”) does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka’s application portal without a valid written search agreement in place for the position will be considered Otsuka’s sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
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