Associate Manager Medical Information

Date Posted: 01/06/2026

Hiring Organization: Rose International

Position Number: 495194

Industry: Biotech/Healthcare

Job Title: Associate Manager Medical Information

Job Location: Santa Monica, CA, USA, 90404

Work Model: Onsite

Shift: 8 to 5 PM PST

Employment Type: Temporary

FT/PT: Full-Time

Estimated Duration (In months): 12

Min Hourly Rate($): 50.00

Max Hourly Rate($): 55.00

Must Have Skills/Attributes: Pharmaceutical, Project Management, Regulatory, SOP

Experience Desired: Knowledge and understanding of Kite’s marketed and investigational products. (5 yrs); Ability to provide analysis and evaluate clinical, biomedical and scientific data. (5 yrs)

Required Minimum Education: Bachelor’s Degree

Preferred Education: Master’s Degree

**C2C is not available**

Job Description

Education and Experience

• Pharmacy, Nursing or Medical/ Life Sciences degree/advanced degree or equivalent (PharmD preferred)
• Experience in MI or working in a healthcare environment preferred.
• Experience in the pharmaceutical industry or a MI vendor preferred.
• Experience in Cell Therapy, Hematology or Oncology preferred
  
  

Knowledge and Skills

• Excellent written, verbal and interpersonal communication skills, and the ability to work well in multidisciplinary teams, across geographies
• Ability to create and provide clear communication of scientific data for different audiences, including members of the public
• Knowledge and understanding of Client’s marketed and investigational products
• Knowledge of applicable regulatory and legal requirements for the provision of MI in the pharmaceutical environment, with understanding of regional or country regulations related to the provision of MI services
• Ability to provide analysis and evaluate clinical, biomedical and scientific data
• Ability to develop and maintain good working relationships with departmental and cross-functional colleagues
• Understanding of internal and external stakeholder needs and priorities
• Serve as an advocate for MI affiliate or Global MI
• Demonstrates Client core values and Leadership Commitments
• Has a strong attention to detail, excellent project management and problem-solving skills, and ability to think creatively
• Good organizational and work planning skills and ability to manage multiple projects in a fast-paced environment
• Awareness of digital solutions for communicating with healthcare providers and patients
• Previous experience with problem-solving and project management preferred
  
  

Job Overview

• Responds to unsolicited medical requests regarding Client products from HCPs, members of the public, and internal Client colleagues. Responses are provided in a timely manner using approved standard documents, up-to-date literature support and other resources
• Uses scientific and MI expertise to drive strategic initiatives and empower key stakeholders, HCPs, patients and other requestors with globally aligned resources that enable timely, informed decisions and improved patient outcomes
• Prepares global resources in collaboration with local affiliate teams (TA specialist team). Prepares local resources (affiliate MI specialist team). Vendors may be used
• Identifies, reports and records adverse events and product complaints in a timely manner in accordance with SOP. May be asked to provide medical review for promotional and/or medical materials
  
  

Responsibilities

Routine responsibilities may include the following

• Respond to unsolicited requests for medical and scientific information regarding Client products and documents in the request handling system (MiQ)
• Researches and collaborates with cross functional colleagues to provide response to complex requests. TA specialist responds to complex requests from affiliate MI and internal colleagues
• Create, update, and participate in review and quality check of MI response documents in accordance with local laws and regulations
• MI specialist collaborates with affiliate MI and relevant internal partners who may include medical affairs, development, regulatory, global patient safety and operations, commercial, to manage global response topics and content
• MI specialist prepares data on file to support response documents and complex requests
• Maintain document repository with regular/routine review of approved documents for new data from regulatory updates, scientific conferences, up-to-date literature searches, proactive literature surveillance, or newly published materials
• Understand the needs and preferences of internal and external partners and customers
• Review and provide analysis of MI databases for trends, customer insights and data gaps to guide content development and prepare customer interaction reports to share with internal stakeholders
• May oversee and/or evaluate external consultant writers
• MI specialist provides process and product training to colleagues and vendors as required
• Support departmental strategic initiatives to address major activities within TA (product launches, labelling updates, patient engagement etc.)
• Identify, report and record adverse events and product complaints in a timely manner in accordance with SOP
• Participate in MI activities and projects in line with global and regional strategic MI plans
• Works under supervision of manager or colleague
• **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
• **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
  
  

Benefits

For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).