What are the responsibilities and job description for the Medical Information Specialist position at ATR International?
We are seeking an Associate Manager Medical Information - I for a very important client.
This role consists of both Medical Reviewer for Promotional Review and Medical Information.
- As a Medical Reviewer, this team member will be an integral part of the Promotional Review Committee and the Medical Review Committee. This team member will be responsible for ensuring the medical and scientific accuracy of submitted materials as well as verifying that statements are adequately supported by appropriate evidence and the cited data.
- As a Medical Information Consultant, this team member will be an integral part of the US and Global Medical Information (MI) team who demonstrates therapeutic and product knowledge of Kite Cell Therapy products to optimize internal and external customer communications.
- This will be a remote-based position but must be able to attend weekly meetings that are generally set within Pacific Standard Time business hours
- Serving as a medical reviewer for US and global materials submitted to the medical and promotional review committees
o Ensure medical and scientific accuracy of US and global materials
o Ensure all claims and statements are supported by adequate scientific references and are cited appropriately
o Perform all medical reviews in a timely and expedient manner by the requested due date
o Attend and participate in all regularly scheduled and ad hoc review committee meetings
o Support and collaborate with cross-functional partners (Regulatory, Legal, Commercial, Scientific Communications, Patient Services, Market Access etc.) to achieve mutual understanding and consensus
- Researching and preparing responses for MI inquires, as well as interfacing with and supporting MI escalation's from the US and Global Medical Information vendor/call center:
o Serves as the subject matter expert for MI on Cell Therapy product(s) and associated therapeutic area(s)
o Create and deliver timely responses to unsolicited medical information inquiries/requests from HCPs
o Assist with creating/developing Standard Response Documents (SRDs) for product portfolio, as needed
The ideal candidate will possess the following qualifications:
Maintain an advanced level of medical knowledge including but not limited to the disease area of focus, product mechanism of action, therapeutic area clinical and real-world data, and the competitive landscape.
Knowledge/Skills:
- Excellent written, verbal and interpersonal communication skills
- 2 plus years of experience in medical writing, medical information/drug information, and/or relevant clinical experience
- Working knowledge of the Veeva platform (preferred)
- Ability to work well in multi-disciplinary teams
- Ability to manage multiple projects in a fast-paced environment
- Must have a strong attention to detail, excellent project management and problem-solving skills, and thinks creatively
Specific Education and Experience Requirements
- Advanced scientific or medical degree (MD, PhD, PharmD or equivalent)
- Promotional review experience in the Pharmaceutical or Biotech Industry
- Prior corporate experience in hematology/oncology, immune-oncology or related therapeutic area is highly preferred
Salary : $40 - $55