Join the IQVIA team, where diversity and inclusion thrive in a workplace committed to improving patients' lives. We recognize that our employees are crucial to our mission's success and have been acknowledged as a fantastic workplace. At IQVIA, we provide benefits and programs to empower you to develop and advance in your career. We are particularly interested in attracting individuals with drive and initiative, individuals who are ready to propel their careers forward and contribute to driving performance.
As a global leader in commercial solutions, IQVIA is dedicated to delivering impact both nationally and internationally. Our collaborative teams play a vital role in ensuring that biopharmaceuticals, medical devices, patient support services reach those who need them. We offer valuable insights to customers and demonstrate product value to payers, physicians, and patients. Whether acting as a sales force to physicians or providing education to patients or prescribers, you can contribute to delivering real-world medical breakthroughs with the right experience. Explore the possibilities and be part of shaping a healthier future with us.
In partnership with our client, we are actively searching for experienced Oncology Medical Science Liaisons (MSLs) to deliver on our commitment to serve patients.
The Medical Science Liaison facilitates and develops relationships 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 also participates 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, and codes of conduct.
RESPONSIBILITIES
- Provide field-based medical support to Company's clinical research programs.
- Deliver credible presentations on scientific matters in the disease area of responsibility and about the company pipeline to investigators in company-sponsored 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, supporting clinical trial enrollment.
- Support company clinical development and operations teams through site recommendations, initiation visits, facilitation of communication, and accrual support activities.
- Exchange scientific information with external parties in an accurate, fair, and balanced manner.
- Report field intelligence to IQVIA/Client, including competitive information, perspectives about compounds, and the treatment landscape.
- Establish and maintain close working relationships with site management & monitoring staff to facilitate the initiation and conduct of prioritized clinical trials.
- Support clinical study sites with knowledge and training on the disease, treatment, mode of action, and new data on investigational molecules in a compliant manner.
- Assist in the preparation and conduction of advisory boards.
- Consult with physicians, pharmacists, and other medical professionals to refer appropriate patients to clinical trial sites and review clinical practice topics as requested.
- Act as the point of contact with thought leaders for investigator-initiated studies within the company pipeline.
- Participate in site selection by suggesting sites and investigator names for potential research collaborations or educational roles, ensuring scientific integrity.
- Facilitate medical and scientific field intelligence, maintaining a list of investigators, understanding competitor research activities, and generating insights from investigators.
- Attend scientific meetings and conferences, representing the company at scientific booths at congresses.
- Assist physicians with requests for access to company medicines on a named patient or compassionate use basis, adhering to legal and regulatory requirements.
- Ensure all activities comply with local, global, and national laws, regulations, guidelines, codes of conduct, and company policies.
- Identify and categorize key opinion leaders (KOLs) in the therapy area.
- Work with stakeholders to enhance the company's reputation and demonstrate partnership qualities to clinicians.
- Coach and develop scientific speakers through clinical training and build relationships with advocacy organizations.
- Serve as a scientific resource for marketing, medical, and clinical teams, sharing insights proactively.
- Identify and profile investigators and institutions for observational registries and investigator-initiated trials.
- Manage territory, projects, CRM data, and input data timely.
- Exchange information with thought leaders and gather insights on new treatment options, ensuring compliance.
- Adhere to all legal and compliance requirements, including reporting drug risks and completing mandatory e-learning courses.
- Represent IQVIA professionally as an ambassador at all times.
REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES
- Experience in the pharmaceutical or healthcare environment, or an equivalent combination of education, training, and experience.
LI-CES
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
We are an equal opportunity employer. All qualified applicants will receive consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status by law.
The potential base pay range for this role is $200,000 to $265,000 annually. Actual offers may vary based on qualifications, location, schedule, and additional compensation or benefits.
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