Pipeline CSM, Immunology

AbbVie · Remote; Seoul, Seoul, Korea, republic of

  • Senior
  • Full-time
  • Posted 2026-09-03
  • Confirmed live on 25 September 2026

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Job description

Job Description
• Position: Pipeline Clinical Science Manager, Immunology

• Reports to: Therapeutic Area Head, Immunology

• Location: Seoul, South Korea
PRIMARY FUNCTION

Clinical Science Manager (CSM) are key members of the affiliate medical department. These field-based roles focus on interacting with, and supporting the needs of, investigators participating in priority sponsored studies. Clinical Science Manager (CSM) work to communicate information and facilitate dialogue about AbbVie’s investigational products, and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures (see Note 1, below) and accepted standards of best practice.

Clinical Science Manager (CSM) serve to enhance the scientific credibility of the Company with established and emerging clinical investigators as well as key scientific institutions and collaborative study groups, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of requests for scientific and medical information. Clinical Science Manager (CSM) also participate in close partnership with affiliate-based Site Management & Monitoring staff in the initiation, oversight and follow-up of clinical studies. They also interface with other key members of the affiliate medical department - for example: Medical Managers, Medical Advisers, Clinical Research Managers and functions such as Health Economics and Outcomes Research, Market Access and others as appropriate - relevant to the therapeutic area for which the Clinical Science Manager (CSM has responsibility, and work collaboratively and cross-functionally with other in-field members while retaining functional independence They maintain a high level of scientific knowledge to ensure credible dissemination of scientific information and informed scientific dialogue with key external stakeholders.
Notes:

1. An Acceptable Practices Policy exists in all affiliates, and governed by the Affiliate Compliance Committee, to describe activities permitted by this role.

2. This Job Description does not apply to those employees whose primary job function relates to the monitoring or management of clinical studies.
JOB RESPONSIBILITIES:

• Ensure a strong medical and scientific presence for Abbvie in investigational sites and key scientific centers by facilitation of clinical research and of interventional phase 1-3 trials with Abbvie drugs, while supporting requests for medical and scientific information on products or areas of therapeutic interest to Abbvie

• Establish and maintain a close working relationship with Site Management & Monitoring staff and partner in facilitating the initiation and conduct of prioritized Abbvie-led clinical trials through site feasibility assessment, site engagement and training, defining recruitment issues and answering query from the sites.

• Provide scientific and technical leadership to ensure professional and credible relationships with investigators.

• Consult with physicians, pharmacists, and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the investigator or referring sites.

• Act as the point of contact with external thought leaders to facilitate Sponsor-initiated study (SIS) ideas with AbbVie pipeline assets and requests for support to the local and global medical teams as appropriate.

• Deliver credible presentations on scientific matters in the disease area of responsibility and about AbbVie’s pipeline to investigators in Abbvie-sponsored interventional research.

• Participate in the selection process to identify appropriately qualified external experts the Company would wish to engage in collaborative efforts – such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.); while ensuring a high level of scientific or educational integrity in these collaborative efforts.

• Identify opportunities for R&D collaborations with key institutions and thought leaders and liaise with the Search& Evaluation team and Discovery or Clinical Development teams to facilitate further assessment.

• Facilitate medical and scientific field intelligence – for example, maintain a list of investigators/potential investigators within a given TA, understand competitive research activities in active or planned study sites, generate insights from investigators on challenges and opportunities for AbbVie-sponsored clinical trials – and communicate, where appropriate, within the Company.

• Attend relevant internal and external scientific meetings and Conferences.

• Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requiremen

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