Medical Science Liaison

2 weeks ago

Singapore Novasyte Full time

PURPOSE


The Medical Science Liaison facilitates and develops the relationship with the medical/scientific community including physicians and medical centers, by communicating scientific and medical therapy area related information to investigators and institutions.

They provide information on research developments, and new concepts in medical treatment.

The Medical Science Liaison will also participate in close partnership with Site Management & Monitoring staff in the initiation, oversight, and follow-up of clinical studies.

This is done in a strictly scientific, non-promotional manner, and in full compliance with applicable laws and regulations, guidelines, codes of conduct.


RESPONSIBILITIES

  • Provide fieldbased medical support to Company's clinical research programs
  • Deliver credible presentations on scientific matters in the disease area of responsibility and about company pipeline to investigators in companysponsored interventional research.
  • Engage with clinical trial site investigators and staff to understand enrollment/screening barriers from a medical perspective and work with the site and client to find potential medical solutions. Aiming to support clinical trial enrollment.
  • Provide support to company clinical development and operations teams through site recommendations, initiation visits, facilitation of communication, and accrual support activities
  • In an accurate, fair and balanced manner, exchange scientific information with external parties
  • Report field intelligence to IQVIA/Client including competitive information, perspectives about compounds, and the treatment landscape.
  • Establish and maintain a close working relationship with site management & monitoring staff and partner in facilitating the initiation and conduct of prioritized Company clinical trials.
  • Supports clinicals study sites with knowledge and training on the disease, the treatment, the mode of action and new data on investigational molecules in a compliant manner
  • Supports and aids in the preparation and conduction of advisory boards
  • Consult with physicians, pharmacists, and other medical professionals, in compliance with relevant laws and regulations, to refer appropriate patients to clinical trial sites and review clinical practice topics as requested by the investigator or referring sites.
  • Act as the point of contact with thought leaders for investigatorinitiated study (IST's) ideas within company pipeline assets.
  • Participate in the site selection process by suggesting sites and investigator names to help identify appropriately qualified external experts the Company would wish to engage in collaborative efforts such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.); while ensuring a high level of scientific or educational integrity in these collaborative efforts.
  • Facilitate medical and scientific field intelligence including maintaining a list of investigators/potential investigators within a given therapy area, understand competitor research activities in active or planned study sites, generate insights from investigators on challenges and opportunities
  • Attend relevant scientific meetings and conferences and may represent company in scientific booths at congresses.
  • Ensure that all activities and interactions are conducted with due regard to all applicable local, global, and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.
  • Identify, and categorize key opinion leaders (KOL) with an interest in the designated therapy area.
  • Work with identified stakeholders to establish and enhance the reputation of the company as required and demonstrate themselves to be a partner of choice for consultant clinicians interested in the designated therapy area.
  • Coach, and develop scientific speakers who are actively interested in the designated therapy area through oneonone clinical training on approved clinical slide sets. Act as a clinical resource with professional, and advocacy organizations with the objective of developing relationships
  • Serve as scientific resource to, marketing, medical and clinical as appropriate gathering insights and sharing them proactively.
  • Identify, and profile communitybased investigators, and institutions in order to assess their ability to participate in observational registries, to conduct investigatorinitiated trials, participating in company sponsored studies
  • Territory management, project management and CRM mastery and timely data input
  • Reactively and balanced information exchange with thought leaders and insights gathering on new treatment options in development to better serve patient needs and in compliance with applicable laws, rules and regulations
  • Comply with all legal requirements of the role, all IQVIA compliance requirements as well as the respective requirements of the customers are met. Reports of drug risks are

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