Medical Science Liaison, IBD Pipeline
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: Field-based role in the United States; listed locations include Los Angeles and South San Francisco, California. Preferred states of residence are California and Arizona. Applicants should live within 30 miles of a major airport and within 50 miles of the established territory. Business travel by air or car is required for up to 70% of the time. Relocation benefits are not available.
Salary: $161,280–$299,520 annually, plus a possible discretionary annual bonus.
Company
is a biotechnology company that discovers and develops medicines for serious and life-threatening diseases.
What you will do
- Provide clinical, scientific, health economic, and value-based information about IBD disease states, approved medicines, and pipeline products.
- Engage healthcare providers, population health decision makers, patients, thought leaders, investigators, and related organizations across the assigned region.
- Co-create and execute local medical strategies, engagement plans, clinical priorities, and customer-focused activities with regional and internal partners.
- Support Phase I–IV clinical trials, health economic outcomes research, site selection, recruitment, retention, and collaboration with CRO personnel.
- Respond to on- and off-label questions in accordance with legal, regulatory, compliance, and company guidelines.
- Provide congress support, capture field insights in CRM systems, and contribute to scientific communications, publications, conference data, and educational materials.
Requirements
- Advanced clinical or science degree such as MD, PharmD, PhD, MSN, NP, or PA; BSN candidates must have extensive pharmaceutical field medical experience.
- At least 5 years of related clinical, managed care, or industry experience.
- Proficiency in GCP and ICH standards.
- Knowledge of the relevant therapeutic area, product and safety profiles, managed care, health economics, reimbursement, and pharmaceutical legal and regulatory requirements.
- Ability to travel regularly and use a company-provided vehicle; a motor vehicle record check may be required.
Nice to have
- At least 2 years of experience in the relevant therapeutic area.
- In-depth knowledge of clinical development programs and clinical trial management.
- Experience working in matrixed organizations across clinical operations, clinical development, and medical affairs.
Culture & Benefits
- Work within a science-driven biotechnology organization focused on developing medicines for serious diseases.
- Benefits are available according to the applicable company benefits program.
- A discretionary annual bonus may be available based on individual and company performance.
- Regular external customer meetings and intermittent internal meetings are part of the field-based work environment.
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