Medical Monitor

Medical Monitor (up to Director level)

Location: Ideally commutable to Princeton, NJ | Hybrid | Travel up to 10%- OR remote must be based on the East Coast and happy to travel to the NJ site 1x per month.

This opportunity is to join an innovative, forward-thinking biopharma organization leveraging technology and global partnerships to advance clinical research in autoimmune, neurology, specifically Multiple Sclerosis, and hematology-oncology. The team is committed to developing impactful treatments and driving high-quality clinical trials from early to late phases.

Key Responsibilities

• Design and implement Phase I–III clinical trials in autoimmune and/or hema-oncology areas, ensuring alignment with ICH-GCP and global regulatory standards.
• Provide medical monitoring for clinical trials, ensuring patient safety, data integrity, and quality delivery within defined timelines.
• Collaborate cross-functionally with internal teams and external partners to drive clinical trial progress and issue resolution.
• Maintain effective communications with ethics committees, clinical research sites, patient groups, and regulatory authorities.
• Contribute to medical development activities: training, data interpretation and analysis, participation in safety committees, and preparation of medical research documents.
• Support competitive landscape analysis, clinical development plans, product profile design, and due diligence for new business opportunities.
• Provide medical expertise and insights for portfolio strategy and project development.

About You

• MD (Doctor of Medicine) required - Autoimmune/ Neurology
• Minimum 3 years of direct clinical trial experience in autoimmune and/or hema-oncology indications.
• Hands-on experience with study design, trial execution, medical monitoring, and data analysis in a pharma, biotech, or CRO environment.
• Understanding of local and global regulatory requirements and GCP.
• Strong communication and interpersonal skills for cross-functional collaboration.
• Flexibility to work across time zones; willingness to hold calls with international teams as needed.
• Strong English language and ability to speak Mandarin.

Why Join?

• Salary range is $200-250,00 plus benefits.
• Contribute to innovative clinical programs in areas of high unmet medical need.
• Work with a collaborative, globally minded team focused on advancing science through technology and partnerships.
• Opportunity for professional growth with a clear path up to the Director level.
• Hybrid work environment with reasonable travel expectations (up to 10%).

Ready to make an impact in advancing next-generation treatments? Apply now and help shape the future of clinical research to nbuckland@i-pharmconsulting.com

#medicalmonitor #clinicaldevelopment #multiplesclerosis