McKesson Corp is a Fortune 7 company and is one of the largest providers of medicines, pharmaceutical supplies and health information technology (IT) products and services in the United States with revenues of $208.4 billion in 2018. The company was founded in 1833 by John McKesson and Charles Olcott in New York with a focus on importing and wholesaling pharmaceutical products. United by our ICARE values, McKesson's 78,000 employees work together every day to make better care possible for patients around the globe.

We take pride in our culture of connection and believe in a workplace where everyone can be their full, authentic self. We welcome and encourage veterans, individuals with disabilities and others with diverse perspectives to join our growing team. Your unique perspective and experience are valuable assets that can translate into a rewarding career path with us. Apply to join our team and help shape the future of healthcare!

Position Description

Key Responsibilities

• Serve as the clinical point person managing protocol execution. Responsible for communication and escalation of study related issues as required. Work cross-functionally to ensure clinical program timelines and goals are met. Managing selective open to enrollment (registries, non-treatment, roll over, phase II-IV) and closed to enrollment studies. Mentor Senior Clinical Trial Associate. Exposure to study start up. Ensure trial adherence to ICH/GCP/local regulations. Develop and manage clinical trial budgets. Communicate effectively with internal and external study personnel (investigative staff, vendors, etc.).
• Vendor identification and management (e.g., CROs, IVRS, Reading Centers, etc.); including participating in negotiation of vendor scope of work, budgets, performance management, issue resolution, and quality assessments. Ensure availability of clinical/non-clinical supplies.
• Ensure internal and external systems are updated in a timely manner (CTMS, clinicaltrials.gov). Identify, address, and communicate quality and compliance concerns.
• Participate in development and testing of clinical systems (laboratory, data entry, IVRS, etc.). Provide study-specific direction and mentoring to other staff as appropriate.