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Senior Clinical Trials Specialist
1 month ago
Careers at CTI Clinical Trial and Consulting Services are uniquely interesting, life-changing opportunities to make a difference in the lives of patients. As a Senior Clinical Trials Specialist - Hematology Expert, you will be part of a dynamic team that brings together passion, innovation, and urgency to deliver exceptional results.
About the Role:
This is a field-based position that requires a majority of time spent interacting with external stakeholders, including investigators and clinical thought leaders, while also supporting internal stakeholders and maintaining a high level of therapeutic expertise. The territory being supported is Michigan, Indiana.
Key Responsibilities:
• Medical Engagement: Effectively collaborate and engage in scientific dialogue with TLs to gain insights on the clinical landscape and ensure development of a medical plan that translates into effective launch.
• Strategically engage payers in the pre- and peri-launch phases (with fHEOR and Account Executives).
• Provides medical support to address unsolicited HCP questions in real-time, both in face-to-face interactions and through the Medical on Call virtual capability.
• Develops credible connections with key Thought Leaders (TLs) in hematology through high-quality peer-to-peer scientific dialogue.
• Appropriately document and achieve annual goals.
• Leverages digital capabilities to enhance medical engagement.
Clinical Trial Engagement:
• Provides recommendations and insights to the clinical development team on study feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with home office medical and GDO.
• Liaises with key large accounts to understand clinical barriers to patient access and ensuring equity in access to clinical trials.
• Leads major evidence read-outs with clinical trial investigators e.g., Ph 3 top-line data.
• Support Interventional and Non-Interventional Research (NIR) studies to facilitate patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with home office medical and Global Development Operations (GDO) and as defined by the study scope document.
Requirements:
A MD, DO, PharmD, DNP, or PhD required with minimum 3 years clinical or research experience in hematology OR 3 years as a medical science liaison in lymphoma or multiple myeloma disease landscapes. Cell therapy experience strongly preferred. Proven ability to work independently as well as in cross-functional teams. Current working knowledge of US legal, regulatory, and compliance regulations and guidelines relevant to industry interactions with health-care professionals. Ability to partner and maintain relationships within the medical community. Excellent communication, presentation, and time management skills. Travel expected for this role, including operation of a Company-provided vehicle. Compensation details include an estimated salary range from $150,000 - $200,000 annually, plus incentive cash and stock opportunities based on eligibility.
