Join McKesson, a company with a mission-driven focus on advancing the fight against cancer and making a difference in patients' lives, as a Research Systems Analyst. In this lead role, you will develop and manage projects and tools to ensure assigned tasks are conducted professionally and meet client expectations. You will work closely and effectively with cross-functional teams, ensuring deliverables adhere to SOPs, ICH GCP, applicable regulations, and company policies.
What You'll Do
- Provide the lead project manager role to support business operations across functional units.
- Consult with key team contacts to clearly establish project specifications.
- Ensure schedules are established and necessary budgets are developed and agreed upon prior to project commencement.
- Partner with project sponsors to define project objectives, scope, schedule, and budget.
- Provide direction and ongoing monitoring of team activities to ensure project milestones are met.
- Ensure consistent use of tools and compliance with standard processes and policies.
- Evaluate tool performance, recognize successful results, and take corrective actions when needed.
- Establish project charter and plan, including metrics.
- Manage project execution from planning through delivery, including team, resource, budget, schedule, performance, and quality.
- Communicate effectively with project teams, sponsors, and stakeholders regarding status, risks, and issues.
- Assist in gathering information for tool development and manage requirements documentation and change management.
- Confirm project outcomes by establishing standards and testing requirements.
- Continuously re-evaluate project status, identify issues and risks, and provide recommendations for resolution.
- Initiate changes to internal processes to enhance services and key performance indicators.
- Develop specific work instructions to assist teams in tool utilization.
- Conduct project training for teams as necessary.
- Develop and monitor tool request metrics, including prioritization of new development requests.
- Participate in required educational activities and programs.
- Maintain strict confidentiality.
- Perform related work as required.
What We're Looking For
- Bachelor's Degree
- 3+ years of experience in project management
- Knowledge of applicable sections of the Code of Federal Regulations, FDA Guidance documents, and ICH recommendations for clinical trials
- Knowledge of medical and clinical research terminology
- Strong interpersonal, communication, and organizational skills
- Demonstrated ability to deliver results to the appropriate quality and timeline metrics
- Excellent customer service skills
- Sound judgment and decision-making skills
- Strong software and computer skills, including Smartsheet, clinical trial management systems, clinical trial databases, and MS Office applications
Nice to Have
- Smartsheet Certification strongly preferred
Technical Stack
- Smartsheet
- Clinical trial management systems
- Clinical trial databases
- MS Office applications
Benefits & Compensation
- Compensation: $60,000 to $88,000
- Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
