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Bracco

Produces radiology contrast agents for imaging

Director – Medical Affairs - Oncology

Biology & BiotechUpdated on Nov 12
Full-time

About the Job

Requirements

  • An advanced scientific or clinical degree (MD, PharmD, PhD, PA, NP, MSc, or equivalent) is required.
  • A minimum of five years of relevant work experience is required, including at least three years in the pharmaceutical or biotech industry in Medical Affairs and/or Research & Development.
  • Understanding of clinical trials and FDA approval processes is required.
  • Knowledge of US regulatory rules, including pertinent FDA Guidance for Industry, Office of Inspector General and Department of Justice statutes and regulations, and the overall compliance landscape is required.
  • Ability to comprehend and combine complex data across multiple projects and products is required.
  • Ability to handle multiple demands in a fast-paced environment and interact within multidisciplinary teams is required.
  • Strong analytical ability and excellent written and oral communication and presentation skills are required.
  • Ability to communicate professionally and credibly with external scientific leaders is required.
  • Initiative and independence are required.
  • Legally authorized to be employed in the United States is required.
  • Ability to influence and build relationships across broad global constituencies with competing priorities is required.
  • Strong coaching, facilitation, and organizational skills, and experience working in cross-functional, highly matrixed organizations are required.

Responsibilities

  • Provide medical oversight of and support management of the BED Investigator-Initiated Trials program.
  • Represent US Medical Affairs and support company-sponsored clinical trials and global development programs, including advising on investigator and site selection, liaising with key opinion leaders and investigators, and generating insights.
  • Participate in multidisciplinary strategic planning with clinical development, research and development, regulatory affairs, and commercial functions.
  • Serve as a medical reviewer for Promotional Review Committee and Medical/Legal/Regulatory review processes.
  • Oversee the Medical Information function and serve as the first medical escalation point for unsolicited medical information requests, ensuring responses are scientifically accurate, balanced, compliant, and aligned with regulations and company policies.
  • Serve on the US Medical Affairs–Oncology leadership team and drive assigned programs and initiatives.
  • Collaborate in training sales representatives and US Medical Affairs field personnel on disease management principles and practices and on the attributes and clinical data of marketed and developmental products.
  • Lead the planning, execution, and scientific oversight of advisory boards to gather external expert insights for medical strategy, evidence generation, and patient care initiatives.
  • Establish and maintain relationships with national and international key opinion leaders in the United States and targeted therapy areas, working with Medical Science Liaisons.
  • Serve as the primary contact between Medical Affairs and the commercial team, providing medical and scientific information to external clinicians and organizations as needed.
  • Serve as an internal medical subject matter expert for US Medical Affairs and the broader organization.
  • Provide medical input into field-team tools and resources.
  • Stay current in targeted therapy areas and with current and future competition, including marketed and developmental products.
  • Maintain communication with global Medical Affairs and Clinical Development colleagues to advance related initiatives.
  • Perform other duties requested by the VP of US Medical Affairs–Oncology or senior leadership, and other duties as business needs require.
  • Travel approximately 30% for major national conferences, advisory boards, interactions with scientific leaders and organizations, annual national company meetings, and departmental training sessions and retreats.

Desired Qualifications

  • Clinical care and research experience in the therapeutic areas in which the company has products or developmental assets is preferred.
  • Diagnostic nuclear medicine experience is preferred.
  • Product launch experience is preferred.

About the Company

Bracco

Produces radiology contrast agents for imaging

Bracco Imaging is a global leader in diagnostic medical imaging, focusing on contrast agents and imaging solutions. It develops and sells iodine-based contrast agents that are used during radiology and imaging procedures to make blood vessels and organs easier to see on scans. These agents work by altering the way tissues appear on CT and other imaging modalities, improving visualization of anatomy and pathology. Bracco emphasizes research and development to create products with better visibility and patient tolerability, building a presence in more than 100 countries from its headquarters in Italy. Unlike many competitors, Bracco’s history spans nearly a century, starting as a family business and growing through sustained innovation in imaging chemistry and supportive imaging technologies, aiming to provide clinicians with safer, clearer imaging options to aid diagnosis and treatment planning.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Milan, Italy
Founded
1927

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