Joulé
Temporary Corporate Counsel, Contracts Attorney
Joulé, Alameda, California, United States, 94501
Job Title
Senior Corporate Counsel, Contracts (R&D)
Location
1851 Harbor Bay Parkway, Alameda, California, 94502, USA
Contract Type
Contract (6‑Month, renewable)
Compensation
$140 per hour (Contractor Work Model: Onsite)
Summary / Job Purpose
The Senior Corporate Counsel, Contracts takes a supporting role in setting the material terms of the many business transactions undertaken by the company, drafting and negotiating definitive and ancillary agreements, and organizing processes necessary and helpful for the company to transact efficiently and effectively. This function also plays a transactional oversight role, working with Legal and operational colleagues to help ensure that the company’s R&D activities and transactions are carried out with efficiency and reflect an appreciation for an appropriate level of business and legal risk.
Duties and Responsibilities
Draft, review, and negotiate a wide range of contracts with a high degree of independence in support of R&D organizations (including confidentiality agreements, collaboration agreements, licensing agreements, consulting agreements, materials transfer agreements, simple and complex clinical trial agreements, clinical advisory board agreements, vendor services agreements, manufacturing agreements for cGMP drug supply, etc.). Act as a legal point person for ongoing agreements in support of R&D efforts. Review redlines, supervise negotiations and provide guidance to junior attorneys and contracts managers. Assist with maintaining up‑to‑date form agreements consistent with industry standards and applicable laws. Identify and define operational and legal risks and communicate them to appropriate internal decision‑makers. Cultivate strong and highly effective cross‑functional relationships and communication with internal colleagues to address legal and business questions. Effectively represent the company. Handle miscellaneous legal tasks on an as‑needed basis.
Supervisory Responsibilities
No supervisory responsibilities; may provide direction to other individuals.
Education, Experience, Knowledge & Skills
BS/BA degree in life sciences or related field (advanced life science degree preferred). JD degree required; minimum six to eight years of relevant experience. Admitted to practice law, preferably in California. Experience as an attorney in a law firm or in‑house legal environment in biotechnology or pharmaceutical industry. Complex contract drafting and negotiation experience required, including significant volume of contracts supporting drug R&D activities. Clear and concise verbal and written communication skills; excellent interpersonal communication skills. Strong computer skills (Microsoft Office Suite, document management systems, redlining software). Detail‑oriented with strong organizational skills. Ability to handle multiple tasks simultaneously and re‑prioritize under short time frames. Ability to make complex decisions based on available data; drives to finish on all projects. Works under pressure to meet specific deadlines. Works well independently and in a team environment; addresses differences fairly and equitably. Dedicated to quality, reliability, and highest professional standards in all work tasks. Self‑starter and quick learner with good judgment.
Equal Opportunity Employer
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Reference
Ref: #568‑Clinical
#J-18808-Ljbffr
Senior Corporate Counsel, Contracts (R&D)
Location
1851 Harbor Bay Parkway, Alameda, California, 94502, USA
Contract Type
Contract (6‑Month, renewable)
Compensation
$140 per hour (Contractor Work Model: Onsite)
Summary / Job Purpose
The Senior Corporate Counsel, Contracts takes a supporting role in setting the material terms of the many business transactions undertaken by the company, drafting and negotiating definitive and ancillary agreements, and organizing processes necessary and helpful for the company to transact efficiently and effectively. This function also plays a transactional oversight role, working with Legal and operational colleagues to help ensure that the company’s R&D activities and transactions are carried out with efficiency and reflect an appreciation for an appropriate level of business and legal risk.
Duties and Responsibilities
Draft, review, and negotiate a wide range of contracts with a high degree of independence in support of R&D organizations (including confidentiality agreements, collaboration agreements, licensing agreements, consulting agreements, materials transfer agreements, simple and complex clinical trial agreements, clinical advisory board agreements, vendor services agreements, manufacturing agreements for cGMP drug supply, etc.). Act as a legal point person for ongoing agreements in support of R&D efforts. Review redlines, supervise negotiations and provide guidance to junior attorneys and contracts managers. Assist with maintaining up‑to‑date form agreements consistent with industry standards and applicable laws. Identify and define operational and legal risks and communicate them to appropriate internal decision‑makers. Cultivate strong and highly effective cross‑functional relationships and communication with internal colleagues to address legal and business questions. Effectively represent the company. Handle miscellaneous legal tasks on an as‑needed basis.
Supervisory Responsibilities
No supervisory responsibilities; may provide direction to other individuals.
Education, Experience, Knowledge & Skills
BS/BA degree in life sciences or related field (advanced life science degree preferred). JD degree required; minimum six to eight years of relevant experience. Admitted to practice law, preferably in California. Experience as an attorney in a law firm or in‑house legal environment in biotechnology or pharmaceutical industry. Complex contract drafting and negotiation experience required, including significant volume of contracts supporting drug R&D activities. Clear and concise verbal and written communication skills; excellent interpersonal communication skills. Strong computer skills (Microsoft Office Suite, document management systems, redlining software). Detail‑oriented with strong organizational skills. Ability to handle multiple tasks simultaneously and re‑prioritize under short time frames. Ability to make complex decisions based on available data; drives to finish on all projects. Works under pressure to meet specific deadlines. Works well independently and in a team environment; addresses differences fairly and equitably. Dedicated to quality, reliability, and highest professional standards in all work tasks. Self‑starter and quick learner with good judgment.
Equal Opportunity Employer
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Reference
Ref: #568‑Clinical
#J-18808-Ljbffr