Clinical Study Manager (Oncology)

Are you a passionate and dedicated individual with a strong background in oncology clinical research? Do you thrive in a fast-paced, collaborative environment where your expertise can make a real impact on patient outcomes? If so, we have an exciting opportunity for you to join our team at McKesson Corporation as a Clinical Study Manager (Oncology). In this role, you will lead and oversee the planning, execution, and management of clinical trials for our oncology products, ensuring compliance with all regulatory requirements and delivering high-quality results. We are looking for someone with a deep understanding of oncology clinical research, strong leadership skills, and a commitment to driving innovation and improving patient care. If this sounds like you, we would love to hear from you.

1. Develop and oversee the execution of clinical trial protocols for oncology products, ensuring adherence to timelines, budget, and quality standards.
2. Collaborate with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure successful trial design and execution.
3. Manage site selection, initiation, and monitoring activities, and provide guidance to clinical research associates and other team members.
4. Ensure compliance with all relevant regulations, guidelines, and internal SOPs, and maintain accurate and complete study documentation.
5. Oversee vendor selection, management, and oversight, including contract negotiation and budget tracking.
6. Lead regular study team meetings and provide timely updates to senior management on study progress and potential risks.
7. Identify and implement process improvements to increase efficiency and quality in clinical trial execution.
8. Collaborate with key stakeholders to develop and review study protocols, informed consent forms, and other study-related documents.
9. Participate in site visits, as needed, to ensure protocol compliance and provide training and support to study personnel.
10. Develop and maintain strong relationships with key opinion leaders and investigators to support successful recruitment and retention of study participants.
11. Keep abreast of industry trends and developments in oncology clinical research and apply knowledge to study design and execution.
12. Act as a mentor and resource for junior team members, providing guidance and support as needed.
13. Uphold ethical and professional standards in all interactions and maintain confidentiality of sensitive information.
14. Represent the company at scientific conferences and meetings, presenting study data and contributing to the scientific community.
15. Demonstrate a commitment to patient safety and well-being, striving to improve patient outcomes through innovative and high-quality clinical research.

According to JobzMall, the average salary range for a Clinical Study Manager (Oncology) is $100,000 - $140,000 per year. However, this can vary depending on factors such as the specific company, location, experience level, and education level of the individual. Some Clinical Study Managers in Oncology may also receive additional bonuses and benefits.

Celesio AG is a healthcare and pharmaceutical company, based in Stuttgart, Germany. The company operates in 14 countries around the world and generated revenue of more than 22,000 million euros in 2014. The corporation is part of the American McKesson Corporation who has a 76% stake in the company.