Job Description

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

Works in compliance with principles of Good Clinical Practice and applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards.

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.

Minimum Requirements

* Minimum of three years of clinical research experience

Critical Skills

* Prior oncology research experience
* Study management/project management experience

Additional Knowledge and Skills

* Attention to detail, solid execution, meeting aggressive timelines, strong interpersonal skills and team player. Excellent verbal and written communication skills.
* Must be pro-active team player, flexible, and open to change.
* Works in compliance with principles of Good Clinical Practice and applicable federal, state, and local regulations.
* Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards.
* Experience developing study plans and budgets including risk mitigation strategies.
* Experience in multiple phases of research preferred.

Education/Training

* Bachelors degree in clinical or scientific discipline (or equivalent experience)

Working Conditions

* General Office, may require travel by air or automobile approximately up to 10% of the time.
* Large percent of time performing computer-based work is required.

Must be authorized to work in the US. Sponsorship is not available for this position.

McKesson is an Equal Opportunity/Affirmative Action employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.Qualified applicants will not be disqualified from consideration for employment based upon criminal history.

McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to McKessonTalentAcquisition@mckesson.com . Resumes or CVs submitted to this email box will not be accepted.

Current employees must apply through the internal career site.

Join us at McKesson!