Clinical Science Liaison - Interventional Oncology and Embolization

Location

Maple Grove, MN | United States

Job description

Additional Location(s): N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.                

Clinical Science Liaison Position – Interventional Oncology and Embolization

About the Role:

At Boston Scientific, the Americas field based “Clinical Science Liaison” (CSL) is responsible for assisting the Boston Scientific Interventional Oncology and Embolization (IO&E) clinical and medical department with clinical trial site activities including on-site investigator and personnel support. The CSL is responsible for all field-based support of BSC IO&E clinical trial initiatives. The CSL has an assigned territory autonomously managing, developing, and growing clinical activities/initiatives achieving key clinical and medical objectives.

TERRITORY – WEST AREA: IDEAL LOCATIONS: CHICAGO, DENVER, LOS ANGELES, DALLAS

Your Responsibilities Include:

• Assist Boston Scientific Clinical Development department with company sponsored clinical trials focusing on clinical trial site identification, site initiation, site protocol education, and ongoing support. Identify key issues that are accelerating or inhibiting patient recruitment, quality data collection or patient retention. Recommend research sites that can perform well delivering patient enrollment and quality data. Support principal investigator and provide up to date information that may improve patient recruitment and/or data quality. Provide medical insights and updates on key findings affecting the study performance.
• Provides input into the development of global clinical trial strategies.
• Participate in IO&E franchise and study-level feasibility activities through providing key site-specific knowledge including patient pathways and operational execution.
• Interface and function as an expert on the clinical trial protocol(s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trials.
• Contribute to the trial specific site feasibility / selection strategy and collaborate with the Clinical Trial Manager (CTM) and CRO to support the site start-up process as needed.
• Oversee and track patient recruitment process and pro-actively identify ways to prevent recruitment delays.
• Proactively work to fully understand all matters that impact the successful patient recruitment and high-quality conduct of the clinical trial at each site, e.g., the Principal Investigator (PI) and site preferences and best practices on clinical trials, standard of care treatments, competing studies etc. Ensure a supportive relationship with clinical sites and trial personnel.
• May attend live and virtual events to assist in responding to questions about clinical trial(s) and other information on Boston Scientific therapies.
• May participate in monitoring oversight activities such as accompanying the CRO/CRA during site visits (This to ensure high quality conduct and execution of the clinical trials according to the protocol and ICH GCP and local regulatory requirements)
• Closely work together with the Medical Affairs colleagues (MSLs) to ensure optimal synergies in the respective site contacts and support.
• Optimize site engagement for a specific trial and across the IO&E franchise to ensure site engagement and quality for the site-level enrollment and execution of every trial.
• Pro-actively identify issues and look for solutions in the assigned clinical trial and timely escalate them to the respective study CTM, CODL, Global Head of Clinical Site Communication, Recruitment and Liaisons, Head of Trial Operations and/or Senior Management, as needed.
• Identify efficiencies, best practices and lessons learnt and ensure they are shared across trials/indications.
• May be asked to provide input to the clinical development strategy/plan.
• Participate in workstreams and provide input to procedures/SOPs/WIs and related document.
• Through scientific exchange, discover novel investigator sponsored research (ISR) ideas. Clearly articulate Boston Scientific strategic interest and fully understand how a concept fits within the strategy. Fully appreciate novel ideas that could significantly impact patient care. Support Investigator Initiated research/study program by discovering and championing innovative ideas, facilitate study start up and provide ongoing consultation. Provide quarterly updates to senior leadership on study progress and medical/scientific insights. Inform Boston Scientific leaders of major milestone accomplishments.
  • Build, maintain, and manage effective professional peer-peer relationships with contracted External Experts (EE), or Key Opinion Leaders (KOL) engaging in bi-directional scientific/educational exchange. Understands medical/scientific barriers that may influence study design, patient enrollment and patient outcomes.

• Investigate and gather field medical intelligence/insights that might affect therapy safety/efficacy, Clinical/R&D strategies, and competitive activities. Communicates knowledge in a simple, coherent, and informative manner to internal stakeholders.
  • Identify clinical insights and knowledge gaps and be able to articulate the impact and magnitude of the findings.

What We’re Looking For:

Required Qualifications:

• Bachelor’s degree required, terminal degree in clinically related area preferred (PharmD, PhD, MD/DO)
• Over 5 years’ experience functioning in an industry medical or clinical role supporting clinical trials.
• Record for creating, managing, and completing medical/scientific related projects.
• Clinical trial acumen; preferably having clinical trial experience and knowledge of GCP.
• Ability to travel extensively within the US (North America) and within assigned territory. Some international travel may be required.
• Ability to operate a car and maintain a valid driver’s license.
• Physical ability to operate interventional instrumentation.

Preferred Qualifications:

• Oncology experience or demonstrated ability to master new therapeutic areas.
• Industry experience in a clinical, medical, or scientific liaison role
• Field experience
• Medical devices experience
  

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