Medical Science Liaison (Msl) Reproductive Medicine
Medical Science Liaison (MSL) Reproductive Medicine
Medical Science Liaison (MSL) Reproductive Medicine Apply locations Milan, Italy time type Full time posted on Posted 2 Days Ago time left to apply End Date: March 30, 2025 (30+ days left to apply) job requisition id R0032819
Job Description: Medical Science Liaison- MSL At Ferring Pharmaceuticals, we help people around the world build families and live better lives.
We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women's health, gastroenterology and urology.
Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.
The MSL RM (reproductive medicine) is a full field-based scientific expert to external and internal stakeholders reporting to the Italy Medical Affairs Director.
This role is in charge of delivering non-promotional information exchange, establishing scientific collaborations and supporting data and insight generation.
Your day at Ferring The MSL represents a medical-scientific reference point for the products of the therapeutic area of competence at national level.
Main areas of responsibility are as below:
Customer facing scientific expert supporting and developing partnerships with external customers Carries out identification, mapping and updating of external opinion leaders.
Maintains the KOL database.
Identifies opportunities for collaboration and builds collaboration with main KOLs and external medical experts.
Provides Medical information services and support to customers.
Reactively respond to unsolicited and documented queries from HCP.
Conducts fair and balanced scientific exchanges with KOL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings, potential research collaborations.
Provide scientific/educational presentations to HCP: Reactively: on products (on-label and off-label indications), on compounds in development.
Proactively: on disease area management.
Supports organisation and - if required - carries out Adv 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.
Gather and report field Insights to support the local/regional/global strategy Collect, analyse, and report actionable insight from HCP related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment.
Contribute to dissemination of insights and information within the company.
Report spontaneous adverse events and product-related quality complaints in accordance to global and local SOP.
Medical/scientific liaison support in oversight & execution of data generation activities Identifies opportunities to generate data.
Coordinates and facilitates unsolicited Investigator-Initiated Study (IIS) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs' objectives.
Supports implementation & follow up of the R&D projects and Company Sponsored Studies (CSS) incl.
post-marketing projects (investigators site and external expert identification and evaluation, feasibility, recruitment, investigator meetings, study management, investigators query) when appropriate.
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.
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.
Attends appropriate scientific congresses to interact with HCPs, develop knowledge in relevant therapy areas and to produce congress summaries for dissemination to HCPs.
Collect and understand competitor activity in therapeutic areas relevant to Ferring's interests and strategy – updating internal team.
Support cross-functional teams and carry out Medical operations in the cluster/country.
Supports cross functional teams (sales, marketing, market access) in response to enquiries and deliver scientific presentations on the disease area and on the product.
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 Manager and cross-functional teams.
Compliance with GCP, SOP's, guidelines and regulatory requirements within the country.
Competencies and Skills BioMedical, Scientific University education.
Medical practice or research career (hospital and/or hospital related, university research, pharmaceutical industry research or Medical Affairs).
Ideally previous experience as biologist/embryologist in a Fertility center.
Ideally proven experience and successful track record as an MSL or Medical Affairs department professional in a previous company.
Experience in Reproductive Medicine or Gynecology area preferred.
Experience in delivery scientific presentations and development of relationships with KOL is strongly preferred.
Ideally, knowledge in data analysis and statistics for purpose of understanding clinical study results.
Ideally, current working knowledge of regulatory, legal and compliance regulations and guidelines relevant to industry interactions with health-care professionals.
Comprehensive understanding of the pharmaceutical industry and clinical operations.
Strong communicator.
Fluent in English.
People come first at Ferring Get inspired from our commitment to advocate for everyone's right to build a family, no matter who you are, where you live or who you love.
Our inclusive support package – "Building Families at Ferring" provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role.
Parental leave for both birthing and non-birthing parents.
Extended support on family building journey.
Making a difference in the life of millions of people means we succeed by working together.
Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member's contributions.
Imagine the power of your career when it's Ferring + You.
Behind our purpose… There's you If our mission and your vision are aligned, please apply!
We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status.
Location: Ferring Italy
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