Henlius USA Inc.
Corporate Paralegal- part time
Apply below after reading through all the details and supporting information regarding this job opportunity. Henlius USA, Inc. located in Milpitas, CA, focuses on developing and delivering high-quality, innovative, and affordable medicine to patients worldwide to treat a range of chronic and life-threatening diseases with a focus in oncology and autoimmune diseases.
Job description To provide paralegal support to attorneys with respect to contracts and IP, including managing multiple projects within required timelines, reviewing, revising and drafting a broad range of contracts and interpreting contract provisions, conducting research, preparing memoranda and other documents under the supervision of an attorney. Typical agreements include confidentiality disclosure agreements, clinical trial agreements, consultant agreements, vendor agreements, material transfer agreement, SOWs and amendments.
Primary Responsibilities
Reviewing and revising contracts and ensuring adherence to company policies, other requirements, and conformance to master agreements
Reviewing appropriate terms and conditions, coordinating with internal legal counsel and business units for acceptance of any non-standard agreement terms where necessary
Coordinating and tracking a large volume of contracts and providing advice and guidance regarding contract requests
Organizing, analyzing, cross-checking and validating information
Preparing correspondence, checking and editing legal forms and documents for accuracy
Gathering, assembling and analyzing information from a variety of sources to prepare and format contracts and other documents for legal review
Maintaining electronic and physical filing systems for contracts and other legal documents
Performing project administration responsibilities and other assignments as directed
Education/Experience Bachelor’s degree and minimum of 5 years’ paralegal or equivalent experience. Specific experience in contract review and administration is required. Certificate program in paralegal studies desirable. Thorough knowledge of legal principles and practice, legal research techniques and legal and contract terminology preferred.
Skills
Strong analytical, research and critical thinking skills with the ability to comprehend difficult instructions and maintain written records
Highly detail-oriented
Ability to produce high quality work
Must work quickly, efficiently, and calmly in a high-volume, high-demand environment
Discreet in handling sensitive and confidential information
Excellent professional ethics, integrity and judgment
Ability to work accurately, to follow instructions precisely and to handle multiple priorities efficiently and effectively
Self-motivation with excellent interpersonal and communications skills, including tact, diplomacy and flexibility
Ability to function independently as well as have effective interactions with team members
Excellent verbal and written communication skills required
Strong computer literacy (including Microsoft Office) and ability to learn specialized computer programs
Knowledge of or experience in the pharmaceutical or biotech industry desired
Extensive knowledge and experience in clinical trial agreements and related clinical documents desired
Reading and writing proficiency in Mandarin required
Hours Starting part-time, 3 days per week, may increase in the future.
Location First year on-site in Milpitas, CA; FWH/hybrid possible afterwards
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Apply below after reading through all the details and supporting information regarding this job opportunity. Henlius USA, Inc. located in Milpitas, CA, focuses on developing and delivering high-quality, innovative, and affordable medicine to patients worldwide to treat a range of chronic and life-threatening diseases with a focus in oncology and autoimmune diseases.
Job description To provide paralegal support to attorneys with respect to contracts and IP, including managing multiple projects within required timelines, reviewing, revising and drafting a broad range of contracts and interpreting contract provisions, conducting research, preparing memoranda and other documents under the supervision of an attorney. Typical agreements include confidentiality disclosure agreements, clinical trial agreements, consultant agreements, vendor agreements, material transfer agreement, SOWs and amendments.
Primary Responsibilities
Reviewing and revising contracts and ensuring adherence to company policies, other requirements, and conformance to master agreements
Reviewing appropriate terms and conditions, coordinating with internal legal counsel and business units for acceptance of any non-standard agreement terms where necessary
Coordinating and tracking a large volume of contracts and providing advice and guidance regarding contract requests
Organizing, analyzing, cross-checking and validating information
Preparing correspondence, checking and editing legal forms and documents for accuracy
Gathering, assembling and analyzing information from a variety of sources to prepare and format contracts and other documents for legal review
Maintaining electronic and physical filing systems for contracts and other legal documents
Performing project administration responsibilities and other assignments as directed
Education/Experience Bachelor’s degree and minimum of 5 years’ paralegal or equivalent experience. Specific experience in contract review and administration is required. Certificate program in paralegal studies desirable. Thorough knowledge of legal principles and practice, legal research techniques and legal and contract terminology preferred.
Skills
Strong analytical, research and critical thinking skills with the ability to comprehend difficult instructions and maintain written records
Highly detail-oriented
Ability to produce high quality work
Must work quickly, efficiently, and calmly in a high-volume, high-demand environment
Discreet in handling sensitive and confidential information
Excellent professional ethics, integrity and judgment
Ability to work accurately, to follow instructions precisely and to handle multiple priorities efficiently and effectively
Self-motivation with excellent interpersonal and communications skills, including tact, diplomacy and flexibility
Ability to function independently as well as have effective interactions with team members
Excellent verbal and written communication skills required
Strong computer literacy (including Microsoft Office) and ability to learn specialized computer programs
Knowledge of or experience in the pharmaceutical or biotech industry desired
Extensive knowledge and experience in clinical trial agreements and related clinical documents desired
Reading and writing proficiency in Mandarin required
Hours Starting part-time, 3 days per week, may increase in the future.
Location First year on-site in Milpitas, CA; FWH/hybrid possible afterwards
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