Medical Science Liaison (MSL) -Maternal-Fetal Immunology - EST/CST

Amplity•Richmond, VA

20h•Remote

About The Position

The MFI Medical Science Liaison (MSL) has a specialized focus that complements Medical Science Liaison (MSL)/ Clinical Trial Liaison (CTL) responsibilities. The key aspects and objectives of this role are: Support and enhance the enrollment of ongoing clinical studies, specifically in rare maternal-fetal diseases. The primary focus is on increasing recruitment into ongoing Phase 3 trials. Relationship Building: Establish and maintain strong relationships with healthcare professionals (HCPs) and key opinion leaders (KOLs) in the Maternal-Fetal Immunology space. Identify and build relationships with KOLs in adjacent specialties, including neonatology, pediatric hematology, and transfusion medicine, to support disease and trial awareness within institutions that are. Disease and Trial Awareness: Drive awareness of both the rare diseases being studied and the associated clinical trials and disease registries. Scientific Collaboration: Foster collaboration with HCPs and other stakeholders to support educational and data generation activities, ensuring alignment with scientific and organizational goals. Market Development: Engage and educate markets that may have limited familiarity with rare maternal-fetal diseases, including the introduction of new prenatal testing options, thus expanding the reach, and understanding of these areas. Scientific Insights: Collect valuable feedback and insights from the medical community to inform trial strategies and improve program outcomes. Non-Promotional Information Dissemination: Share accurate and relevant medical and scientific information in a non-promotional manner to support trial and disease awareness. The MFI MSL plays a critical role in the success of the program by ensuring high scientific standards, fostering collaboration, and aligning with the organization's broader strategies.

Requirements

Advanced degree e.g., Ph.D, Pharm. D, MD, MSN, NP/PA or equivalent education required from an accredited institution required.
MFM or OBGYN, experience either as an MSL or in clinical setting strongly preferred.
Neonatology or Hematology experience is also acceptable.
MSL/CTL experience desired.
Strong knowledge of clinical and scientific principles in the Obstetrics/Gynecology Neonatology, Maternal/Fetal Health desired.
Understanding of the clinical trial processes and the ability to provide support to clinical research initiatives.
Exceptional communication and interpersonal skills, with the ability to present scientific information and build new markets, is important.
Skilled at building and maintaining key relationships with healthcare professionals and key opinion leaders.
Strong clinical acumen, high learning agility a self-initiative needed.
Excellent organizational and time-management skills, with a results-oriented mindset.
Ability to work independently and collaboratively in a dynamic, fast-paced environment.
Willingness to travel 70% within the assigned multiple state region needed.
Excellent technology skills e.g., PowerPoint, Excel, digital meeting platforms
Valid driver's license with safe driving record required.
Successfully pass all required Amplity and client training

Responsibilities

Collaborate with the Director of MSLs to execute the overall program strategy, ensuring alignment with MSL/CTL organizational objectives.
Boost recruitment into the Phase 3 trials
Build and maintain trusted relationships with healthcare professionals, key opinion leaders (KOLs), clinical trial investigators/sites, and other stakeholders in assigned region.
Gather and report scientific insights from the field to inform cross-functional teams and support organizational decision-making.
Engaging in the exchange of scientific data and other medical and/or scientific information with external stakeholders
Represent the organization at scientific meetings, conferences, and advisory boards as needed.
Serve as a subject matter expert staying current with relevant scientific literature, clinical guidelines, and advancements.
Support for strategic initiatives across Medical Affairs, Clinical Development, and other internal teams.
Act as a liaison between internal teams and external stakeholders to support scientific exchange and collaboration.
Operate with the highest ethical and professional standards, adhering to all applicable laws, regulations, and organizational policies.
Ensure that all MSL and Clinical Trial activities are conducted in compliance with relevant guidelines and regulations.