Responsibilities:

1. Assists in the management of all aspects IITs, COOPs, and Third Party Trials
2. Adjusts priorities and demonstrates adaptability, identifies and implements new or different ways to achieve goals
3. Identifies, analyzes, and communicates problems, issues, and opportunities. Develops and implements effective solutions to achieve desired outcomes
4. Lead Medical Affairs Ops process improvement initiatives
5. Completes assigned tasks within functional team
6. Assist with any special projects as assigned
7. Expected to provide valuable input on plans & decisions
8. Evaluates and manages time and resources effectively
9. Provide mentorship within functional team
10. . Knowledge of the drug development process in the planning and management of clinical studies
11. Develops and delivers information in a clear and concise manner within company and clinical research guidelines
12. Listens actively and shares relevant information with others
13. Develops effective working relationships with business partners to achieve business goals
14. Demonstrates an understanding of study drug and industry competition
15. Understands the disease state and treatment options
16. Develops project plans and manages multiple projects to achieve goals within established timelines
17. Ability to create and deliver a presentation
18. Collaborates to identify strengths and developmental areas; creates, owns, and implements professional development plan
20. Responsible for implementing plans & decisions in collaboration with Operation Manager

Qualifications
Required Competencies-Knowledge, Skills, and Abilities:
1. Ability to communicate effectively in the English language in person, by phone and in writing
2. Excellent organizational skills
3. Ability to work collaboratively, effectively, and productively in diverse organization structures
4. Ability to work in a team-oriented, collaborative environment
5. Ability to demonstrate leadership capabilities
6. Solid computer skills and practical knowledge of MS Word, Excel, PowerPoint and project management software
7. Ability to create and deliver presentations to management or team members
8. Must be flexible and manage change easily
9. Ability to work positively within a continually changing environment
10. Ability to problem-solve
11. Ability to effectively prioritize and execute tasks in a high-pressure environment

Education & Experience:
1. BS/BA in a health-related science or RN
2. Six to eight years of experience in clinical research, clinical coordinator, clinical nurse role or an equivalent combination of education and experience
3. Knowledge of drug development process, FDA, ICH, and GCP guidelines
4. Oncology experience is strongly preferred
5. Experience working with Cooperative groups strongly preferred
6. Investigator Initiated experience required
7. Drug forecasting experience preferred

WORK ENVIRONMENT
1. Corporate office environment
2. Cross-functional interactions

SUCCESS FACTOR
Deliver quality work, dependability, innovation, integrity and compassion