Regional Clinical Science Liaison, North America

Overview

Regional Clinical Science Liaison, North America

Reports to Senior Director, Clinical Development & Medical Affairs

The Regional Clinical Science Liaison (CSL) plays a pivotal role in advancing breast cancer clinical trials at Menarini Stemline by cultivating robust relationships with clinical trial sites and investigators, with a primary focus on optimizing patient enrollment.

Responsibilities

• Site Engagement and Relationship Management:
  • Identify and evaluate potential clinical trial sites and investigators specializing in breast cancer, ensuring alignment with study protocols and patient eligibility criteria.
  • Build and sustain strong relationships with investigators and site staff participating in breast cancer trials.
  • Serve as the primary point of contact for site inquiries related to recruitment and enrollment, providing timely and accurate information.
  • Facilitate seamless communication and collaboration between sites and the study team to align recruitment objectives and strategies.
• Recruitment Strategy and Support:
  • Collaborate with sites to develop and implement effective patient recruitment strategies tailored to breast cancer studies, considering patient demographics, tumor characteristics, and current treatment paradigms.
  • Provide expert guidance and support to sites facing recruitment challenges, leveraging knowledge of breast cancer patient advocacy groups, support organizations, and relevant medical conferences.
  • Proactively monitor site enrollment progress in partnership with the study team to identify and address potential roadblocks or inefficiencies.
  • Collaborate with CRAs to ensure smooth study conduct and resolve any recruitment-related issues in breast cancer trials.
• Trial Education and Scientific Communication:
  • Deliver accurate and current information regarding the company's breast cancer pipeline products to healthcare professionals through various channels, including one-on-one meetings and scientific presentations.
  • Support site initiation activities, including comprehensive training on breast cancer-specific recruitment procedures and providing essential study materials, and updates on protocol amendments.
  • Support organizing regional investigators’ meetings.
  • Actively gather insights from healthcare professionals concerning study protocols, site‑specific requirements, and the evolving breast cancer treatment landscape, informing the company's research and development strategies.
• Compliance and Quality Assurance:
  • Maintain a thorough understanding of relevant regulations, GCP, and ICH guidelines pertaining to clinical trial conduct and patient recruitment, with a specific emphasis on breast cancer research.
  • Ensure all recruitment activities adhere to ethical standards and applicable laws and regulations.
  • Participate in ongoing training to enhance expertise in breast cancer research, treatment advancements, and best practices in patient recruitment.
  • Escalate any site concerns or issues to the Clinical Development team and Senior Director for timely resolution.

Qualifications

• An advanced degree in a life-science field (MD, Ph.D. or Pharm.D.) is preferred.
• Minimum of 5 years of experience in clinical research, with a strong focus on breast cancer clinical trials.
• In-depth knowledge of breast cancer, including disease subtypes, staging, treatment options, and the current research landscape.
• Experience in site management, monitoring, or recruitment, strong understanding of clinical trial operations, GCP, and ICH guidelines.
• Excellent communication, interpersonal, and presentation skills, with the ability to clearly articulate complex scientific concepts.
• Proven ability to build and maintain strong relationships with key stakeholders.
• Strong organizational and time‑management skills, with the ability to prioritize tasks effectively.
• Ability to work independently and collaboratively within a team.
• Willingness to travel up to 60% or more as needed covering clinical trial sites across multiple territories.

Base Salary Range of $180,000 - $230,000 plus 25% annual bonus & 35% Long‑term Incentive Bonus. Menarini Stemline offers generous compensation and benefits packages, including Fidelity 401(k) (with company match), Anthem Premier PPO and HDHP insurance plans, Company paid Basic Life & AD&D insurance and pre‑tax FSA/HSA programs.

Menarini Stemline is committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.