Global Channel Management, Inc.
Senior Paralegal - Biotech & Pharma Contracts Specialist
Global Channel Management, Inc., Marlborough, Massachusetts, us, 01752
Description
In this role, you will leverage over 5 years of direct contract experience within the Biotech and Pharmaceutical industry. You will be responsible for a variety of functions including clinical trial management, corporate governance, litigation support, and intellectual property matters. Your expertise in contract management and drafting will play a crucial part in driving our legal operations forward.
You will require a strong service mindset, possess excellent contract negotiating and influencing skills, and maintain expert knowledge of contract structures, principles, and automation functionalities. Exceptional communication skills and the ability to work independently in a dynamic environment are essential, as is a critical and innovative thinking approach to problem-solving.
Skills
In-depth knowledge of clinical trials, corporate governance, and litigationProven experience in contract management and intellectual propertyExcellent attention to detail and strong business acumenStrong stakeholder management and interpersonal skillsHigh proficiency in Microsoft Word; ability to learn other Microsoft Office applicationsFamiliarity with Contract Management systems (Agiloft preferred)Capacity to learn new software programs/systems quickly
Responsibilities
Draft, negotiate, and administer contracts with minimal supervisionCollaborate with business functions to draft and negotiate various agreements including master service agreements and confidentiality agreementsManage contract template processes and incorporate best contracting practicesOversee the electronic contract management system and assign tasks to attorneysIdentify risks and propose alternatives for effective solutionsDevelop improvements to the contracting process and ensure ongoing complianceMonitor contracts throughout their life cycleAdvise internal teams on contracting processes and recommendationsEnsure compliance of templates and agreements with legal standards and best practicesParticipate in other legal projects as necessary
Employment Type: Full-Time
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In this role, you will leverage over 5 years of direct contract experience within the Biotech and Pharmaceutical industry. You will be responsible for a variety of functions including clinical trial management, corporate governance, litigation support, and intellectual property matters. Your expertise in contract management and drafting will play a crucial part in driving our legal operations forward.
You will require a strong service mindset, possess excellent contract negotiating and influencing skills, and maintain expert knowledge of contract structures, principles, and automation functionalities. Exceptional communication skills and the ability to work independently in a dynamic environment are essential, as is a critical and innovative thinking approach to problem-solving.
Skills
In-depth knowledge of clinical trials, corporate governance, and litigationProven experience in contract management and intellectual propertyExcellent attention to detail and strong business acumenStrong stakeholder management and interpersonal skillsHigh proficiency in Microsoft Word; ability to learn other Microsoft Office applicationsFamiliarity with Contract Management systems (Agiloft preferred)Capacity to learn new software programs/systems quickly
Responsibilities
Draft, negotiate, and administer contracts with minimal supervisionCollaborate with business functions to draft and negotiate various agreements including master service agreements and confidentiality agreementsManage contract template processes and incorporate best contracting practicesOversee the electronic contract management system and assign tasks to attorneysIdentify risks and propose alternatives for effective solutionsDevelop improvements to the contracting process and ensure ongoing complianceMonitor contracts throughout their life cycleAdvise internal teams on contracting processes and recommendationsEnsure compliance of templates and agreements with legal standards and best practicesParticipate in other legal projects as necessary
Employment Type: Full-Time
#J-18808-Ljbffr