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Role Summary: A team leader and subject matter expert with sales contracts review and negotiation experience, specifically in the pharmaceutical and medical device manufacturing industries. Able to build training materials, monitor queues, perform quality checks (QC) and provide feedback to team members based on project guidelines and client instructions.

Responsibilities and Duties:

• Negotiate third party sales agreements and other contract-types as needed based on client guidance
• Liaise between the client and global delivery teams
• Work in developing project guidance materials and project knowhow documents and imparting training to the team on the same
• Build productivity and delivery reports and analytics
• Maintain personal and team records of work done
• Train team members on processes including contract review and management
• Perform QC based on project guidelines and client instructions
• Create project specific documentation and guidelines
• Contribute to process improvement ideas and actively participate in process improvement initiatives
• Manage client timelines and ensure SLAs (turn around time, Quality) are met individually

Required Skills/Abilities:

• Ability to read and understand contractual language to identify and flag client risks and suggest mitigation as per client’s playbook
• Experience in Contract Review in the Pharmaceutical Industry, with a strong preference for experience in medical device manufacturing
• Proven track record in leading teams and delivery within the pharmaceutical and medical device sectors
• Flexible to work in rotating shifts
• Ability to comprehend questions and respond appropriately (writing and verbal)
• Knowledge of MS Office – Word including redlining and document comparisons
• Logical thinking and good decision-making abilities
• Work independently, self-learning attitude, disciplined, sincere and need less supervision
• Responsible for compliance with ISO standards and other confidentiality

Education and Experience:

• Licensed Attorney with 4-5 years’ experience of team and client leadership, contract negotiation, review, and drafting, preferably within the pharmaceutical and medical device manufacturing industries

Additional Skills:

• Familiarity with regulatory requirements specific to medical device manufacturing
• Experience with compliance standards related to medical devices, such as FDA regulations

Benefits: Health, vision, dental, 401k and tuition discount

Company Information

Integreon is a trusted, global provider of award-winning legal and business solutions to leading law firms, corporations and professional services firms. Our highly trained, experienced staff of over 3,000 employees globally service a comprehensive range of client needs that require scale and expertise, enabling clients to become more operationally efficient. Integreon works with corporations and law firms who rely on our team’s experience and expertise in documents, administrative and business services. With delivery centres on three continents, Integreon offers multi-lingual, around-the-clock support, as well as onshore, offshore and onsite delivery of our award-winning services.

If you are exceptional at what you do, we would love to put you to work in an exceptional company in an exceptional position. We are One. We are On. Follow us https://www.linkedin.com/company/integreon/ Visit us at www.integreon.com