Site Support Contracts Legal Analyst
- Experience Level
- Experienced (non-manager)
Under general supervision, serve as Single Point of Contact (SPOC) for escalation, review, and negotiation of agreements for assigned Site Service project sites.
Provide contracting intelligence to support assigned studies and the wider company, as required.
Accountable for overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.
Assess and review the contracting landscape and lead the collection, interpretation, analysis and dissemination of accurate guidance to operational contacts, including identification of legal requests vs. business decisions
Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Accountable for specialist legal, operational and financial contracting support provided by the team to ensure efficient
Inform team members of completion of contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents in line with project timelines.
Support the delivery of activities as determined by the appropriate team lead and conducts specific tasks under guidance of senior staff.
Experience and Skills:
Strong interpersonal communication and organizational skills
Good attentional to detail and ability to work on multiple projectsa
In-depth knowledge of clinical systems, procedures, and corporate standards.
Experience negotiating with or on behalf of Investigator Sites for Clinical Research
Excellent negotiating and legal writing skills.
Effective communication, organizational, planning and interpersonal skills.
Ability to work independently and to effectively prioritize tasks.
Ability to work within a matrix team environment
Ability to work on multiple projects.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements, including local regulations, SOPs and company’s Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Proven ability to work on multiple projects balancing competing priorities
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.