Translational Medicine Expert – Dermatology, Associate Director

Novartis; Basel; Hybrid; CHF 122.500 - 227.500; Vollzeit

Benefits dieser Stelle

Competitive base salary

Performance-based bonus

Long-term equity awards

Flexible working options

Paid parental leave

Zusammenfassung

Novartis in Basel, Switzerland is seeking a Translational Medicine Expert (TME) to provide medical and scientific leadership for early and late global programs. Responsibilities include developing strategies and leading cross-functional teams to ensure successful drug development.

The ideal candidate is a board-certified dermatologist with an MD and a Ph.D. in dermatology/immunology, along with at least 5 years of relevant experience. The position offers a competitive salary, performance bonus, equity awards, and extensive benefits including flexible working options.

Qualifikationen

• At least 5 years’ experience in a pharmaceutical/biotech company, CRO, or academic medical center.
• Recognized expert driving success for studies and respected within R&D and Development.

Aufgaben

• Develop and implement strategies for early global programs.
• Act as a key leader in late-stage clinical projects support.
• Collaborate closely with teams to ensure operational excellence.
• Lead study-specific teams and clinical trial teams.

Kenntnisse

Medical expertise in dermatology

Leadership skills

Clinical pharmacology knowledge

Research development

Fluent English

Ausbildung

Doctoral degree, MD

Board certified Dermatologist

Ph.D. in dermatology/immunology

Jobbeschreibung

Job Summary

Location: Basel, Switzerland

As a Translational Medicine Expert (TME), you will provide medical and scientific expertise and leadership to:

• Drive success of early global programs, develop and implement strategies to achieve Transition Decision Point (TDP)
• Drive success of late global programs by developing and implementing strategies, which lead to clinical pharmacology and profiling packages that meet regulatory requirements and support differentiated and competitive drug labeling.
• Support translational research in developing new indications, endpoints and biomarkers, using in vitro, in vivo, or in silico methods.
• Provide scientific expert assessments and support for in‑licensing opportunities, including due diligences.

Key Responsibilities

• Early Clinical Projects (Phase I / II, “Discovery”) – Develop, in collaboration with the dermatology TA and work with teams to carry out strategies for the Translational Medicine component of drug development projects from research to TDP in single or multiple indications, including post‑indication expansion (PIE) projects.

• Late‑Stage Clinical Projects (post‑TDP, “Profiling”) – In collaboration with the dermatology TA Head, act as a key leader in developing the Phase 2–3 and post‑approval profiling strategy for drug programs, representing TMDP on the Global Project Team along with other TM line functions. Provide support for dose selection, study design, and other clinical pharmacology matters throughout the development cycle. Oversee conduct and interpretation of studies prioritized to support the pivotal trials, such as special populations, drug‑drug interactions, mechanism of action assessments, Pediatric Investigational Plan, etc.

• Translational Research (TR; indication seeking, endpoint and biomarker development) – In collaboration with the dermatology TA Head, BR research scientists, and other TM line functions (BMD, CS&I, PCS, PKS), develop strategies to identify initial or expansion (PIE) indications and obtain sufficient evidence to fund these ideas.

• Business Development and Licensing (BD&L; in‑licensing and out‑licensing compounds) – Participate on BD&L teams as the TM representative.

• General Responsibilities

  • Responsible for clinical monitoring and integrated safety data review during and after the live phase of a study.
  • Provide medical and scientific leadership and expertise to all line functions on the study team.
  • Represent clinical Translational Medicine aspects to health authorities and other stakeholders (e.g. payers, patient advocacy groups).
  • Oversee publication strategy for TM studies; lead writing of scientific publications and present study results externally where appropriate.

• Leadership

  • Lead study‑specific teams/clinical trial teams in partnership with other line functions.
  • Lead BR‑sub‑team(s) on Global Project Teams for late‑phase programs.
  • Collaborate closely with other TM (especially CS&I) and non‑TM (especially Project Management) line functions to ensure operational excellence, continued urgency, and close attention to timelines, costs, and subject burden in balance with high scientific standards and innovation.

Essential Requirements

• Doctoral degree, MD
• Board certified Dermatologist
• Preferably Ph.D. within dermatology/immunology
• At least 5 years’ experience in a pharmaceutical/biotech company, CRO, or academic medical center, or related experience
• Innovation: Seeks out new clinical discovery opportunities and approaches to reach TDP
• Recognized expert in field, driving success for individual studies and projects; respected by colleagues across R&D, Development, and externally
• Fluent oral and written English

Benefits & Rewards

Competitive base salary, performance‑based bonus, long‑term equity awards, insurance plans, retirement plans, wellbeing resources, global recognition programs, flexible and hybrid working options, and a minimum of 14 weeks paid parental leave.

Expected Annual Base Salary Range For Role

• 122,500.00 - 227,500.00 CHF Annual

The base salary offered is determined based on gender‑neutral objectives such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and will be reviewed periodically upon joining Novartis.

In addition to base salary, you may be eligible for a performance‑based bonus depending on certain performance parameters. Long‑term equity awards granted at group level may also be part of the package.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Commitment to Diversity and Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Accessibility and Accommodation

Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process or in order to receive more detailed information about the essential functions of the position, please send an e‑mail to [e-mail] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.