Medical Science Liaison

ESSENTIAL DUTIES & RESPONSIBILITIES

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  Medical Communication & Education:
  * Provide medical information to physicians, treatment center personnel, and patients regarding Kaneka Medical America products.
  * Lead content development for medical communications and education.
  * Conduct orientation sessions for clinical, marketing, and sales teams on clinical practices, research projects, guidelines, and adverse event handling.

  
  
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  Collaboration & Relationship Management:
  * Regularly interact with sales, marketing, and clinical teams to address scientific inquiries.
  * Establish and maintain relationships with key customers, opinion leaders, treatment centers, and patient groups.
  * Engage with physicians and medical personnel at existing and potential LIPOSORBER customer sites.

  
  
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  Clinical Study Support:
  *Support all new and ongoing clinical studies and related activities.

  
  

*Assist in daily tasks related to clinical development projects and clinical study protocols.

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• Scientific Insights & Presentations:
  * Present scientific information at professional meetings as needed.
  * Gather insights from key opinion leaders to conduct gap analyses and support strategic planning.
• Emotional Intelligence Skills:
  * Demonstrate empathy, adaptability, excellent communication, and interpersonal skills.

OTHER RESPONSIBILITIES

• Maintain complete and open lines of communication with other personnel, functions, or departments to facilitate operations and interaction in the organization.
• Keep manager informed of status and progress, ensuring that regular and periodic communication takes place.
• Maintain professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks and keeping abreast of industry trends and related compliance issues within the area of responsibilities.
• Maintain professional conduct, attendance, and high ethical standards in the work place, complying with company's policies and procedures.
• Fulfill mandatory training requirements applicable for department and job duties as appropriate.
• Perform other duties and responsibilities as required or requested by supervisor or Management.
• Assist with overseeing external vendors working on the study.
• Assist with site medical monitoring, data management, IRB application and interaction, pharmacovigilance, and other critical activities for FSGS post-approval study.
• Assist with clinical study protocol and protocol amendments.
• Prepare for clinical documents, e.g., protocols, annual report updates, case report forms and clinical study reports, monitoring plans, and budget as requested by supervisor or Management.
• Assist management with new sites joining the adult and pediatric FSGS post-approval study.
• Support functional area management with medical content creation and review for targeted therapeutic areas.

Enthusiastic - Shows intense and eager enjoyment and interest
Team Player - Works well as a member of a group
Loyal - Shows firm and constant support to a cause
Dedicated - Devoted to a task or purpose with loyalty or integrity
Detail Oriented - Capable of carrying out a given task with all details necessary to get the task done well

Doctorate (required)
PHD of Pre-Medicine (required)
Bachelors of Pre-Medicine (required)

2 years: Therapeutic area experience: Cardiology & Nephrology (preferred)
1 years: Managing clinical studies (required)
1 years: Medical device/Pharmaceutical industry (required)
2 years: Scientific/Medical affairs (required)

Skills