Medical Science Liaison Manager (m/w/d)

Region: Kiel, Bremen, Oldenburg

Our client is a leading internationaly operating biopharmaceutical enterprise.
We are searching as soon as possible for a dedicated and experienced

Medical Science Liaison Manager (m/w/d)

Region: Kiel, Bremen, Oldenburg

  • Bereich:


  • Berufssparte:

    Medical Affairs

  • Arbeitsregion:

    Homeoffice in der Region

  • Art der Anstellung:


  • Kennziffer:


  • Aktualisierung:


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Your tasks

  • Identifies, develops and maintains collaborative relationships with current and future KOLs, key centers and local collaborative groups and develops required qualitative and quantitative reports.
  • Works with KOLs to develop clinical therapeutic concepts that support the advancement of the science associated with Celgene´s advances in the therapeutic area.
  • Works with local patient organizations in collaboration with designated person at EU headquarter.
  • Implements and disseminates high quality complex scientific information, innovative medical education materials and research concepts to KOLs incl. speakers preparation and slide kit development.
  • Supports development and implementation of internal training plan which continuously monitors and updates knowledge of disease area.
  • Serves as the face for the company to centers of influence in supporting visiting professorships, guest lecturers, symposia workshops that are within the goals of local therapeutic audience team.
  • Fosters medical and scientific information exchange from the medical community to the company.
  • Supports or makes clinical and scientific presentations to regional healthcare audiences aligned with central medical education programs.
  • Organizes local advisory boards with key stakeholders in designated area and educational symposia at local congresses and forwards key finds to Lead RML Inflammation & Immunology.
  • Supports KOLs in developing concepts and protocols for IITs that support the companies products.
  • Manages budget for medical education programs.
  • Effectively supports communication activities from IITs, in collaboration with relevant medical communication manager and publication team.
  • Supports field sales and corporate account efforts related to presenting clarity around clinical and scientific information supporting therapeutic decisions in patient care.
  • Works with marketing and sales to ensure prioritization of key accounts.
  • Identifies new opportunities, that support key product messages, based on medical and scientific data for both internal and external customers.
  • Supports appropriate screening process to identify potential investigators for company initiated clinical trials, collaborate with clinical trial groups to evaluate requests and assess capacity. Oversees implementation of approved clinical trial support activities.
  • Provides support for answering unsolicited off-label questions and questions regarding new indications and future products.
  • Collects and reports competitive intelligence derived from centers’ of influence and scientific meetings.
  • Develops Congress reports /summary slide decks of important national congresses.
  • Execution and placement of MA activities (including Medical Education programs, IITs).
  • Is involved in territory business planning and prioritization of business expenses.
  • Ensuring of scientific up to date information of speakers and KOLs in respect to company products and therapeutic areas.
  • Ensures compliance with GMA SOPs, GCP and ICH, compliance policies and procedures, relevant country reports regulations as well as with legal and ethical standards.

Your qualifications

  • Strong identification with the company’s values.
  • Medical or scientific experience (M.D., Ph.D. or Pharm.D. preferred, but not required).
  • Specific knowledge in dermatology and/or rheumatology and/or immunology and scientific research experience preferred.
  • Documented medical or scientific experience in therapeutic area (e.g. subspecialty board certification, academic track record).
  • Knowledge of commercialization and business practices.
  • Field force experience preferred.
  • Knowledge of Regulatory Affairs, Drug Safety, legal and compliance environment.
  • Network of customer contacts.
  • Experience or knowledge of Health System and Health Care decision making.
  • Project Management and Medical Affairs skills (clinical trial design, clinical data analysis, basical statistical techniques, literature knowledge).
  • Attitude for understanding and applying the law and regulatory policies to business situations.
  • Strong customer orientation, science based and marketing minded.
  • Excellent communication and presentation skills, scientific and non-scientific, throughout all levels and geographies of an organization, in English and German, proven experience of successful to read cross-functional teams.
  • Fluency in English (both oral and written, presentation skills).
  • Willingness to travel.
  • Valid driver‘s license.

Ihre Ansprechpartnerin

Bettina Cöppicus
Senior Personalberaterin


Optares ICM GmbH & Co. KG
Bettina Cöppicus
Heiligengeist Höfe 8
26121 Oldenburg