Regional Medical Science Liaison
Tardis Medical
United Kingdom
13d ago


Regional Medical Science Liaison (RMSL)


JobTitle : Regional Medical ScienceLiaison (RMSL)

Department : Medical Affairs outsourced through TardisMedical

ReportsTo : Tardis Medical & Manager ofField-Based Medicine in Europe

Anywhere in UK (home office andtravel 50 - 70% + / -)

Territory : UK / Denmark Region

Contract : Permanentwith Tardis Medical

The Opportunity

Providing aunique and strong collaborative network in support of our innovative pipelineacross therapeutic areas including gastroenterology, cardiology, inflammation,autoimmunity, and pain.

You will have the opportunity to make a difference inpeople’s lives every day. The function of the Regional Medical Science Liaisonis fundamental to both execution of our Clinical Development programs andbuilding appropriate connections to the external medical community,communicating scientific / clinical information and collecting impactful insightsto enhance our strategic objectives.

In this role,you will support activities across both Medical Affairs and ClinicalDevelopment objectives for a portfolio of pipeline products.

You will serve asa key interface with clinical trial sites across all development programs,working closely with Clinical Development and Clinical Operations.

Additionally, you will collaborate with Medical Affairs to identify and engageopinion leaders within the medical community to communicate non-

promotionalscientific and medical information regarding disease state and / or pipelineproducts across a range of therapeutic areas.

  • What you will dive into;
  • You will serve as the primary interface between the sponsor and clinicaltrial sites across all development programs, working closely with ClinicalDevelopment and Clinical Operations to ensure the successful execution of highquality clinical studies.

    You willadvise and participate in the planning and set-up of clinical studies for yourassigned region.You will collaborateand ensure alignment with local CD / Clinical Operations / CRO colleagues to ensureflawless execution of the clinical trials at the sites in your region.

    ScientificExpertise : You will developdeep scientific expertise across several therapeutic areas, including inflammatorybowel disease, cardiology and chronic pain.

    You will be the subject matterexpert in these therapeutic areas in your region.You will consistently demonstrate that youare a scientifically credible leader and collaborative partner that is highly perceptive,socially intelligent and intuitive

    OpinionLeader Engagement : Youwill cultivate and maintain strong relationships with opinion leaders, clinicalinvestigators and their respective study staff within your assigned region acrossa range of therapeutic areas.

  • Cross-Functional Support : You will provide scientific support toClinical Development, Medical Affairs, Commercial and other cross-
  • functionalcolleagues to ensure the successful execution of key corporate strategies. Youwill support activities, including but not limited to scientific congresses,advisory boards, speaker programs.

    You will share important clinical andscientific insights that you have gathered from your fieldwork tocross-functional teams.

    Compliance : Youwill operate in a highly ethical manner and comply with all laws, regulationsand policies.

    What we expect

  • Ideallyadvanced degree (PhD, PharmD or MD) preferred or Master degree
  • Biotechexperience is a plus
  • Fluentin English and fluency in the language of a local country is required
  • Strongwritten and verbal communication skills, ability to present medical / scientificinformation in a clear and concise manner
  • Adeptat developing relationships and building networks
  • Excellentorganizational skills and results oriented mindset
  • Abilityto influence without authority and negotiate with confidence
  • Abilityto function well, both independently and within a team setting, in a dynamic, fast-pacedenvironment
  • Relevanttherapeutic area knowledge, ideally inflammatory bowel diseases
  • Experiencewith clinical trial design, conduct and evaluation
  • Permanentresidence within region assigned
  • Ableto travel up to 50-70% of time
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