Come and Save Lives with Us!
SERB Pharmaceuticals is a growing international specialty pharmaceutical group that is a dedicated ally to healthcare providers treating patients with critical conditions, focusing on emergency care and rare diseases. We have over 470 employees in 16 countries and a group revenue in excess of €350m.
Our portfolio of 80 rescue medicines makes a real difference in the lives of patients and their caregivers and that gives every one of our employees a sense of purpose.
Our Purpose Is Supported By Our 4 Key Values
- We make patients our priority
- We act with integrity and accountability
- We work together as one team
- We look for better ways forward
Broad Overview
Responsible for establishing, fostering, cultivating and maintaining credible and unbiased medical and scientific dialogue with multiple external entities, including but not limited to external scientific and medical leaders, and Advocates of the group product portfolio, academic medical institutions, disease and patient societies and healthcare professional organisations. The end goal is to act as the conduit for accurate, unbiased and updated clinical, scientific and medical information between the external scientific community in the assigned countries and the company which will support the strategic growth of the Group’s Portfolio in each Country.
As The Medical Science Liaison Your Responsibilities Will Include
Ensure that regional and local medical plans are effectively implemented to support the strategic growth of the Group’s product portfolio in relevant specialities.Provide a world-class field-based expert Medical Service to KOLs, Product Advocates, experts, HCPs and commercial team within the designated countries and therapeutic areas.Identify local medical and patient needs, defining and executing local Medical Plans aligned with the individual country and regional field medical strategy.Engage in scientific exchange and develop / maintain relationships with cooperative groups, medical associations and external experts within countries / therapeutic areas in order to identify unmet medical needs, evidence gaps, obtain insight and optimize the scientific community’s knowledge of the Group’s product portfolio and development activities within compliance.Provide high-quality medical and scientific educational programs, guidance and product training to HCPs and commercial team to support the safe and effective use of our products within compliance.Work closely with the Country & Commercial / Market Access functions to ensure the knowledge and inclusion of company products in local guidelines / formularies, through the best available evidence of the product’s value and effectiveness.Participate in training via quality medical education presentations for internal, new field-based medical staff and field-based sales force.Provide key market insights and field feedback to Medical Director and Country Manager(s).Support publication strategies to ensure rapid and appropriate publication of generated data.Coordinate the IISs at Regional level, ensuring that projects submitted are scientifically sound, acting as IIS Facilitator at the IIS-RC and as a link with the Investigator when required.In collaboration with the Clinical team assist in identification of potential clinical sites, collect feedback on potential clinical development options from multi-disciplinary physicians and support patient recruitment activities as directed.Collaborate and share with Line Manager and Group Clinical / Medical Support Team ideas to overcome challenges and maximize opportunities related to clinical utility of the Group’s product portfolio.Participate in internal project teams for local projects or initiatives as requested by Line Manager / Country Manager.Work closely with Line Manager, Country Teams and Group Clinical / Medical Support Team to optimize time and efficiency within a large geographic area in order to maximize patient outcomes.Ensure compliance with all local laws regulating company activities and that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company values.Support and advise the local Compliance Officer and Line Manager to ensure compliance of activities under Association of the British Pharmaceutical Industry (ABPI) Code of Practice, and the Association of British HealthTech Industries (ABHI) and all applicable regulations applicable.The above duties and responsibilities are not an exhaustive list, and you may be required to undertake any other reasonable duties compatible with your experience and competencies. This description may be varied from time to time to reflect changing business requirements.
To Be Successful In This Role, You Should Demonstrate
Graduate level scientist or pharmacist or MDA post-graduate qualification and / or PhD or equivalent work experience a benefit.Holder of ABPI UK exam a benefitDemonstrated credibility within the medical community.Ability to effectively communicate concepts and ideas with a high degree of independence, professional maturity, strategic thinking with an entrepreneurial spirit.Strong analytic skills and a creative thinker who can solve problems.Excellent interpersonal skills with demonstrated ability to develop networks and maintain business relationships.Proven track record of results.Superior written and verbal communication skills with both internal and external customers in local language and English.Company Benefits
25 annual leave days plus bank holidays and 3 annual company closure days (to be taken between Christmas and New year)Competitive Pension SchemePrivate Medical InsuranceDiscretionary Bonus PlanPaid Maternity and Paternity LeaveAcademic Study AssistanceEyecare vouchersEmployee Assistance ProgrammeSERB Pharmaceuticals is an equal opportunity employer. We offer competitive compensation & benefit packages, challenging opportunities and a culture of working together in a supportive way built on our strong foundation of values. #J-18808-Ljbffr
