Medical Science Liaison at IQVIA

Singapore

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Clinical Research, HealthcareIndustries

Requirements

Ability to facilitate and develop relationships with the medical/scientific community, including physicians and medical centers
Expertise in communicating scientific and medical therapy area-related information to investigators and institutions
Knowledge of research developments and new concepts in medical treatment
Capability to partner with Site Management & Monitoring staff in the initiation, oversight, and follow-up of clinical studies
Strict adherence to applicable laws, regulations, guidelines, and codes of conduct in a non-promotional manner
Ability to engage with clinical trial site investigators and staff to understand and address enrollment/screening barriers from a medical perspective
Skills in site recommendations, initiation visits, communication facilitation, and accrual support
Proficiency in exchanging scientific information accurately, fairly, and balanced with external parties
Capacity to report field intelligence, including competitive information, compound perspectives, and treatment landscape
Experience in maintaining close working relationships with site management & monitoring staff
Knowledge to support clinical study sites with training on disease, treatment, mode of action, and investigational molecules compliantly
Ability to support preparation and conduction of advisory boards
Consultation skills with physicians, pharmacists, and medical professionals to refer patients and review clinical topics compliantly
Role as point of contact for thought leaders on investigator-initiated study (IST) ideas
Participation in site selection by suggesting qualified sites and investigators for collaborations
Ability to facilitate medical and scientific field intelligence, maintain investigator lists, and generate insights on challenges/opportunities
Willingness to attend scientific meetings, conferences, and represent the company at congresses
Capability to assist with named patient or compassionate use access requests under legal requirements
Commitment to conducting all activities in compliance with laws, regulations, policies, and best practices
Skills to identify and categorize key opinion leaders (KOLs) in the therapy area
Ability to work with stakeholders to enhance company reputation as a partner of choice

Responsibilities

Provide field-based medical support to Company’s clinical research programs
Deliver credible presentations on scientific matters in the disease area and company pipeline to investigators in company-sponsored interventional research
Engage with clinical trial site investigators and staff to understand enrollment/screening barriers and work with sites/clients on medical solutions to support enrollment
Provide support to company clinical development and operations teams through site recommendations, initiation visits, communication facilitation, and accrual support
Exchange scientific information accurately, fairly, and balanced with external parties
Report field intelligence to IQVIA/Client, including competitive information, perspectives on compounds, and treatment landscape
Establish and maintain close working relationships with site management & monitoring staff to facilitate initiation and conduct of prioritized clinical trials
Support clinical study sites with knowledge and training on disease, treatment, mode of action, and new data on investigational molecules compliantly
Support and aid in the preparation and conduction of advisory boards
Consult with physicians, pharmacists, and other medical professionals compliantly to refer appropriate patients to clinical trial sites and review clinical practice topics
Act as the point of contact with thought leaders for investigator-initiated study (IST) ideas within company pipeline assets
Participate in site selection by suggesting sites and investigator names for collaborative efforts like research, educational, or advisory roles
Facilitate medical and scientific field intelligence, including maintaining investigator lists, understanding competitor activities, and generating insights from investigators
Attend relevant scientific meetings and conferences and represent company at scientific booths
Assist physicians with requests for access to company medicines on named patient or compassionate use basis, subject to legal requirements
Ensure all activities and interactions comply with applicable laws, regulations, guidelines, codes of conduct, company policies, and best practices
Identify and categorize key opinion leaders (KOLs) with interest in the designated therapy area
Work with identified stakeholders to establish and enhance the company’s reputation as a partner of choice for consultant clinicians

Skills

Scientific Presentations

Clinical Trial Support

Investigator Engagement

Site Management

Disease Area Expertise

Regulatory Compliance

Medical Communication

Field Intelligence

Enrollment Strategies

Clinical Development

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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