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You will be updated with latest job alerts via email Services rendered will adhere to applicable clients SOPs WIs policies local regulatory requirements etc.
Support creation and maintenance of contract templates in accordance with changes in laws regulations or corporate policies.
Support creation and maintenance of fallback language and negotiation guidelines related to contract templates.
Support training on contract templates and fallback language and provide training to first line negotiators and others as required.
Provide specialized support and guidance on the negotiation of CTAs and CDAs to first line negotiators.
Work with the legal department to create risk assessments to support the decision-making process.
Assess risks of legal terms and conditions independently and communicate them to stakeholders such as clinical team law department and internal team where appropriate. Provide guidance to 1st line negotiators stakeholders and others as required.
Lead negotiations on Master Agreements and custom templates or those requiring extensive modifications and identify potential risks to the business.
Participate in contract negotiations on terms and conditions of high-risk and complex agreements and other relevant legal documents as they relate to clinical trials and company/departmental policies (subject to and within the limits of the clients negotiation parameters and the clients form of written contract). For the avoidance of doubt the service shall not have authority to sign contracts on behalf of the clients party.
Coordinate with cross-functional departments to ensure consistency and compliance with process external communications and policies.
Assist in coaching/mentoring staff members.
Liaise with all members of clinical team as needed in addition to representatives of investigator sites academic research organizations contract research organization and site management organizations as directed.
Identify and promote best practices. Adhere to SOPs ethics and departmental compliance as determined by GCDO management as well as R&D companies corporate HCC and QA guidelines.
Collaborate with internal stakeholders to ensure proper dissemination and management of knowledge.
Monitor departmental processes to ensure compliance with corporate policies.
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Manager
Full-Time