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Corporate Counsel, Contracts
Refer job# LDSZ141693
 
Corporate Counsel, Contracts The candidate will draft, review, and negotiate various contracts, such as: confidentiality agreements, materials transfer agreements, research collaboration agreements, government grants, formulation development and manufacturing agreements, clinical trial agreements with clinical sites and contract research organizations, consulting agreements, raw material purchase agreements, preclinical service agreements, bioanalytical testing agreements, compound screening/testing agreements, investor relations agreements. Will assist on statements of Work, Work Orders, Proposals and Quotations (a) emanating from master service agreements and (b) generated as standalone documents in the absence master service agreements. HR related agreements to support agency hires and temp placements. Subscription agreements associated with on-line libraries and software licenses, lease or sublease agreements, and agreements to support facilities repair and maintenance. Quality agreements in collaboration with the head of QA. Term sheets and license agreements under the direction of the GC and such other agreements as requested. Coordinate with GC, internal staff, or external counsel to update contract templates for conformance with regulatory requirements. Select, populate and manage a contract database to record all executed contracts. Use such database to track upcoming contract expiries, payment and other obligations. Draft contract extensions, notices of terminations or amendments, as applicable, in coordination with stakeholder needs.

The candidate should have Law degree from a Canadian university or JD degree from an accredited US law school. Must have 3-4 years of prior work experience in private practice or as in-house counsel at biotechnology or pharmaceutical company. Must have familiarity with terminology typically used within the areas of drug regulatory affairs, quality control, quality assurance, analytical development, process development, manufacturing and clinical trials. Must have good understanding of the work flow and interdependencies among the various departments within a biopharmaceutical company. Must have understanding of intellectual property rights sufficient to collaborate with IP counsel. Prior life sciences research experience is highly desirable. Must have proficiency in contract drafting and template creation.
 
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This particular job is currently not active. However, since our clients regularly share with us similar and other job openings, we strongly recommend that you submit your resume. We shall review your resume and get in touch with you as soon as a suitable vacancy comes up to further discuss your interest in exploring the opportunity. Assisting you is our highest priority.

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