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The Investigator Contracts Lead is responsible for negotiating contracts and budgets with clinical investigator sites, managing escalations, and collaborating with various partners to ensure timely execution of agreements. They lead relationships with key sites, develop processes, and implement solutions for complex contracting needs and challenges in clinical trials.

The Investigator Contracts Lead is responsible for negotiating contracts and budgets with clinical investigator sites, overseeing the Per-Subject Cost process, and managing escalations related to budget issues. They collaborate with legal and finance teams, and lead the contracting activities while ensuring adherence to clinical trial timelines.

The Investigator Contracts Lead is responsible for managing site-facing contract and budget negotiations during clinical trials. This includes overseeing contract execution, managing budgets, resolving escalations, collaborating with various departments, and maintaining relationships with investigational sites.

The Investigator Contracts Lead oversees contract and budget negotiations with clinical investigator sites, manages the Per-Subject Cost process, and ensures timely contract execution for clinical trials. This role includes collaboration with various departments, resolving budget issues, and supervising other professionals involved in site contracting.

The Investigator Contracts Lead is responsible for negotiating contracts and budgets with clinical investigator sites, overseeing contract execution, managing budget issues, and collaborating with various teams to ensure timely site contracting processes for clinical trials.

As a QC Supervisor at Pfizer, you will lead a quality assurance team, analyzing chemical and microbiological products to ensure safety standards are met. Responsibilities include training staff on GMP, conducting laboratory investigations, and supervising QC personnel. You will also manage laboratory budgets and support other departments in troubleshooting and laboratory testing.

As a member of the digital pathology group, you will support drug discovery by performing whole-slide image analysis and developing image analysis algorithms. Key responsibilities include scanning slides, quality assessment, data analysis, generating reports, and maintaining compliance with regulations.