Offer summary

Qualifications:

Bachelor's degree or equivalent experience., At least 4 years of relevant experience in research or project management., Strong organizational and communication skills., Experience with large-scale clinical trials and data management..

Key responsibilities:

Support and manage real world research projects from start-up to closure.

Develop and maintain documentation of study procedures and processes.

Coordinate meetings with internal teams and external partners.

Ensure timely delivery of quality data and manage study financials.

Job description

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care.

What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.

This position will be responsible for the operational aspects of real world research studies. The successful candidate will work closely with cross functional teams to ensure the successful execution of RWR studies through all phases of study conduct including start-up, execution, and closure activities. This role requires collaboration across multiple functions within Ontada, including Biostatistics, Clinical Data Services, and others as required by the study. This person must have excellent communication skills and the ability to multi-task in a fast paced environment while meeting deadlines.

Key Responsibilities

Provide project management support to real world research projects
Develop and maintain comprehensive documentation of study procedures and processes
Manage financials related to study operations
Conduct regular meetings with internal team members and external partners
Ensure timely delivery of quality data
Perform other duties as assigned

Minimum Requirement

Degree or equivalent and typically requires 4+ years of relevant experience.

Education
Bachelor’s degree or equivalent experience

Critical Skills

Strong organizational and time management skills
Excellent verbal and written communication skills
Experience working on large scale clinical trial projects
Demonstrated problem solving abilities
Ability to take initiative and self-motivation
Proven leadership skills
Proficiency in Microsoft Office Suite, including MS Project, Visio, and O365

We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered. For more information regarding benefits at McKesson, please click here.

Our Base Pay Range for this position

$82,100 - $136,800

McKesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees and is committed to a diverse and inclusive environment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age or genetic information. For additional information on McKesson’s full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

Join us at McKesson!

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