<Main Responsibilities> 
Develops, maintains & disseminates high level of scientific and technical expertise in 
therapeutic areas 
•     Keeps up to date with evolving science and evidence base. Ensure this is 
communicated to the appropriate personnel  
•     Prepares and presents critical reviews of scientific publications and congresses, 
internally and externally. 
•     Provides high quality non promotional, medical and scientific 
support/communications to internal and external customers  
•     Attends appropriate scientific congresses to interact with HCPs, develop 
knowledge in relevant therapy areas and to produce congress summaries for 
dissemination to HCPs 
•     Gathers and disseminates competitor activity in therapeutic areas relevant to 
Ferring’s interests and strategy – updates relevant colleagues.   
•     Carries out and supports the development, review and approval of scientific and 
clinical content of relevant promotional and non-promotional materials and activities, 
publication planning, slide-deck development and internal training initiatives, ensuring 
informed, balanced, current, and compliant communications. 
Customer facing medical/scientific expert supporting and developing partnerships with 
external opinion leaders (national or international), patient organizations, authorities 
where required and payers (in support to market access).  
•     Carries out identification and mapping of external opinion leaders 
•     Identifies opportunities and build relationships with National, Regional or Local 
KOLs 
•     Provides field based Medical Affairs support to MSLs in their scientific liaison 
activities as well as coordinating Medical information activities 
•     Organises Ad board meetings, regional/national training 
courses/workshops/events with KOLs 
•     Assists in the organisation and scientific support of key external National and 
Regional events e.g. satellite symposia etc 
Medical/scientific Input, oversight & execution of data generation activities (research, 
clinical studies, RWE, patient programmes, data mining etc) 
•     In support to R&D, Region and CRAs, contributes to the design and execution of 
product / diseases area data generation activities (local, EU, Global), ensure successful 
completion of the trials and their publication.  
For Internal Use - Internal  
•     Ensure that proposals are aligned with medical objectives locally, regionally and 
globally 
•     Ensures and carries out excellence in local execution, timely, legally compliant, 
high-quality performance  
Carry out Medical operations in the cluster/country 
•     Creation of non-promotional and review of promotional materials and activities in 
the appropriate systems/tools and in compliance with SOPs, rules and regulations.   
•     Completes necessary documentations in order to ensure knowledge preservation 
(CRM reports). Use necessary tools to develop and follow up on strategic measures 
(project plans). 
•     In collaboration with cluster/country cross-functional teams, supports creation 
and implementation of strategic and operational plans in the cluster/country, in line 
with Ferring’s global and regional strategy, enabling cluster/country achievement of 
Global Medical Affairs, regional and cluster/country targets  
•     Carries out successful execution of the Medical Affairs strategy and plan in line 
and consultation with the responsible cross-functional teams  
•     Compliance with GCP, SOP’s, guidelines and regulatory requirements within the 
country   
Provides Medical/scientific expert input and support at regional & global level 
•     Provides cluster/country input, field insights at the Global Medical Affairs and 
regional level where required 
•     Acts as TA/product expert/champion at the regional level where required 
•     Supports regional medical activities as appropriate 

Required Education/Qualifications/Skills  
•     BioMedical, Scientific University education ideally to post-graduate degree level 
e.g. MSc, PhD, MD, PharmD  
•     Ideally Master in Pharmaceutical industry/clinical trials 
•     Minimum 3-4 years’ experience in Pharmaceutical Industry or biotechnology 
companies working in Medical Affairs (including KOL management, clinical studies 
oversight)   
•     Current working knowledge of legal, regulatory, and compliance regulations and 
guidelines relevant to industry interactions with health-care professionals 
•     Comprehensive understanding of the pharmaceutical industry and clinical 
operations   
For Internal Use - Internal  
•     Experience of Fertility therapy area and preferably Gastroenterology and/or 
urology   
•     Fluent in English 
Required Ferring Competencies (Behavioural Indicators) 
Customer focus 
Decision quality 
Informing 
Drive for results 
Comfort around high management 
Process management 
Techincal learning 
Peer relationship 
For Internal Use - Internal