Infotree Global Solutions
Senior Medical Science Liaison
Infotree Global Solutions, San Mateo, California, United States, 94403
Position Summary:
We are seeking a highly motivated Medical Affairs Manager with demonstrated experience in providing operational and strategic support for global late-phase (Phase 4) research in the Oncology or other Therapeutic Area (TA). The successful candidate will support the planning and execution of late-phase and real-world evidence studies, including company-sponsored research and Investigator-Sponsored Research (ISR), in close collaboration with internal cross-functional teams and external stakeholders.
This role is ideal for professionals with a background in Clinical Development, Clinical Operations, or Medical Affairs, who are seeking to build upon their experience in phase 4 and real-world evidence research in a dynamic and global environment.
Submit your CV and any additional required information after you have read this description by clicking on the application button.
Key Responsibilities: Provide operational support for global late-phase oncology research programs, including interventional and observational studies. Actively contribute to the planning and execution of Phase 4 clinical trials, Real-World Evidence (RWE) studies, and ISR programs. Schedule meetings via Outlook and secure participation from key stakeholders. Prepare and distribute agendas, presentations, meeting minutes, and follow-up materials. Collaborate cross-functionally with Clinical Development, Regulatory, Legal, Compliance, and external partners to ensure alignment on study goals and timelines. Support development of study protocols, charters, and data dissemination plans in collaboration with scientific and medical leads. Monitor and track key operational metrics, timelines, and budget aspects of assigned projects.
Qualifications: Advanced degree (PhD, PharmD, MD, or equivalent required). 1–2 years of experience in Clinical Development, Clinical Operations, or Medical Affairs. Proven experience in managing operational aspects of clinical or observational research studies. Strong knowledge of clinical trial regulations, ICH-GCP guidelines, and ethical requirements. Exceptional project management, communication, and organizational skills. Ability to work effectively in a global matrix environment and across multiple stakeholders. Proficient in MS Office tools (Outlook, PowerPoint, Excel). Multiple therapeutic area experience strongly preferred. Experience working with global teams and stakeholders.
Submit your CV and any additional required information after you have read this description by clicking on the application button.
Key Responsibilities: Provide operational support for global late-phase oncology research programs, including interventional and observational studies. Actively contribute to the planning and execution of Phase 4 clinical trials, Real-World Evidence (RWE) studies, and ISR programs. Schedule meetings via Outlook and secure participation from key stakeholders. Prepare and distribute agendas, presentations, meeting minutes, and follow-up materials. Collaborate cross-functionally with Clinical Development, Regulatory, Legal, Compliance, and external partners to ensure alignment on study goals and timelines. Support development of study protocols, charters, and data dissemination plans in collaboration with scientific and medical leads. Monitor and track key operational metrics, timelines, and budget aspects of assigned projects.
Qualifications: Advanced degree (PhD, PharmD, MD, or equivalent required). 1–2 years of experience in Clinical Development, Clinical Operations, or Medical Affairs. Proven experience in managing operational aspects of clinical or observational research studies. Strong knowledge of clinical trial regulations, ICH-GCP guidelines, and ethical requirements. Exceptional project management, communication, and organizational skills. Ability to work effectively in a global matrix environment and across multiple stakeholders. Proficient in MS Office tools (Outlook, PowerPoint, Excel). Multiple therapeutic area experience strongly preferred. Experience working with global teams and stakeholders.