Regional Medical Affairs Manager

This is a fully remote position, open to applicants in Illinois.

📋 Description

• Establish and nurture peer-to-peer relationships with national and regional key opinion leaders (KOLs)

• Create and engage in medical communication, education, and training initiatives for KOLs

• Identify gaps in data concerning disease areas or products through clinical insights

• Participate in both local and national congresses

• Assist in the creation, execution, and facilitation of Medical Advisory Boards

• Lead or assist in the design, planning, and implementation of clinical projects, which may encompass interventional, observational, or post-marketing (e.g., Phase 4) studies

• Provide input on study protocols, investigator brochures, statistical analysis plans, and clinical study reports

• Manage study timelines, budgets, and milestones to ensure successful project delivery

• Oversee site identification, feasibility assessments, and Site Initiation Visits (SIVs)

• Support the onboarding and training of investigators and study personnel

• Serve as the primary sponsor representative for CROs and vendors

• Assist in managing vendor performance, timelines, and deliverables

• Contribute to the oversight of sponsor studies, investigator-initiated studies (IIS/IITs), and research collaborations from both scientific and operational viewpoints

• Support ongoing registry programs with an emphasis on data quality and site performance

• Contribute to medical communication and the dissemination of data

• Participate in the development of publication strategies, including abstracts, manuscripts, and presentations at scientific congresses (e.g., AUA, EAU)

• Collaborate with investigators to produce and support manuscripts

• Keep internal stakeholders updated to ensure the timely dissemination of clinical data

• Coordinate with Photocure Global Medical Affairs on various topics (e.g., publication communications)

⛳️ Requirements

• Advanced degree (MD, DO, PharmD, PhD) in life sciences or a related field

• 5+ years of experience in medical affairs or clinical development

• Experience in urology, oncology, or medical device/diagnostics is highly preferred

• Familiarity with bladder cancer or cystoscopy technologies is advantageous

• Background in supporting regulatory submissions and publications is a plus

• Ability to collaborate across functions in a fast-paced, dynamic environment

• Capability to work independently and complete tasks within set deadlines

• Understanding of PhRMA, OIG, and other regulations related to compliant medical communications

• Proven ability to synthesize and communicate medical information effectively

• Exceptional oral and written communication skills

• Willingness to travel approximately 50% of the time, or as required, within the US, Canada, or Europe for KOL visits, SIVs, conferences, etc.

🏝️ Benefits

• Competitive salary and performance-based bonuses

• Comprehensive health, dental, and vision insurance

• Generous paid time off and holiday schedule

• Opportunities for professional development and continuing education

• Collaborative and innovative work environment