• Collaborate closely with internal and external stakeholders for HCP consultancy agreements • Manage HCP contracting tasks and activities • Prepare Conflict of Interest Disclosure Forms • Independently manage assigned business functions • Cultivate relationships with internal support functions • Identify opportunities for process improvement

• Draft, review, and negotiate high-value and complex contracts related to clinical trials, including Clinical Trial Agreements (CTAs), Confidentiality Agreements (CDAs), and other relevant documents • Ensure contracts are compliant with local and international regulations and company policies • Collaborate with internal teams, including legal, clinical operations, regulatory affairs, and finance, to ensure alignment and compliance with contractual requirements • Liaise with external stakeholders, including clients, sites, and vendors, to facilitate the contract negotiation and approval process • Monitor the progress of contract negotiations and address any issues or concerns that arise • Maintain accurate records and documentation related to contracts and agreements • Provide guidance and support to project teams on contractual matters throughout the lifecycle of clinical trials • Participate in the development and implementation of contract management strategies and processes • Ensure timely execution of contracts to meet project timelines and deadlines • Support the resolution of contractual disputes and issues as they arise • Stay up-to-date with changes in regulations and industry standards related to clinical trial contracts • Mentor and provide guidance to junior contract specialists, assisting in their professional development • Participate in training sessions and workshops to enhance the contract management skills of the team

• Support federal acquisition activities throughout the procurement lifecycle • Conduct acquisition planning, market research, and procurement strategy development • Prepare and maintain solicitation packages, including Requests for Quotations (RFQs) and supporting acquisition documentation • Assist with proposal receipt, evaluations, negotiations, and contract award documentation • Prepare contract awards, modifications, and closeout documentation • Support post-award contract administration activities • Ensure compliance with the Federal Acquisition Regulation (FAR) and agency policies

• Draft, review, and negotiate high-value and complex contracts related to clinical trials, including Clinical Trial Agreements (CTAs), Confidentiality Agreements (CDAs), and other relevant documents. • Ensure contracts are compliant with local and international regulations and company policies. • Collaborate with internal teams, including legal, clinical operations, regulatory affairs, and finance, to ensure alignment and compliance with contractual requirements. • Liaise with external stakeholders, including clients, sites, and vendors, to facilitate the contract negotiation and approval process. • Monitor the progress of contract negotiations and address any issues or concerns that arise. • Maintain accurate records and documentation related to contracts and agreements. • Provide guidance and support to project teams on contractual matters throughout the lifecycle of clinical trials. • Participate in the development and implementation of contract management strategies and processes. • Ensure timely execution of contracts to meet project timelines and deadlines. • Support the resolution of contractual disputes and issues as they arise. • Stay up-to-date with changes in regulations and industry standards related to clinical trial contracts. • Mentor and provide guidance to junior contract specialists, assisting in their professional development. • Participate in training sessions and workshops to enhance the contract management skills of the team.