Cardiologist Physician Scientist (Associate Director or Director)

Novartis Group Companies; Cambridge (MA); On-site; USD 204,000 - 440,000; Full time

Job summary

A leading company in biomedical research seeks an Associate Director or Director to lead clinical trials and drug development projects. The role involves overseeing Phase 1 and 2 trials, collaborating with cross-functional teams, and driving innovative strategies in cardiovascular metabolism. Candidates must possess a doctoral degree and relevant industry experience, with a strong emphasis on leadership and communication skills.

Qualifications

• Doctoral degree required, with clinical subspecialty training preferred.
• At least 1-2 years of experience in pharma/biotech; 5+ years for Director level.
• Recognized medical expertise with publications in international journals.

Responsibilities

• Lead global project teams through the PoC phase.
• Responsible for clinical portions of the Integrated Development Plan.
• Communicate clinical team matters to project teams and decision boards.

Skills

Clinical Trials

Data Analysis

Data Monitoring

Drug Development

Drug Discovery

Medical Strategy

People Management

Education

Doctoral degree (MD)

Clinical subspecialty training in cardiovascular disease or endocrinology/metabolic disease

Job description

Job Description Summary

Internal Title: Associate Director or Director

This position will be located in Cambridge, MA and will not have the ability to be located remotely.

#LI-Hybrid

About the role:

The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis, collaborating across the company and beyond to develop powerful new technologies for therapeutic breakthroughs. Translational Medicine (TM), the clinical research arm of NIBR with about 900 associates globally, plays a pivotal role in bringing innovative medicines to patients by translating research advances into new therapies and bridging drug discovery and clinical application.

The TM Discovery & Profiling (TMDP) team, comprising physicians and clinical researchers, drives innovative science from discovery to the patient through the selection, profiling, and development of medicines. TM experts oversee Phase 1 and 2 clinical trials to demonstrate proof-of-concept (PoC) and support Phase 3 development. They are key members of global cross-functional project teams that design and implement early research and discovery projects culminating in clinical PoC studies. These experts collaborate with biology and chemistry colleagues to identify disease targets with unmet medical needs and provide input on clinical development pathways. PoC studies led by TM experts are among the most critical steps in drug development at Novartis. After PoC, if the program proceeds to full development, TM experts continue as key members of the development team through registration.

As a Cardiovascular Metabolism (CVM) TM Expert, you will collaborate with the CVM TM Head or other experienced TM Experts to develop high-value decision strategies for the translational medicine component of drug development projects and lead global cross-functional teams through the PoC phase and beyond.

Job Description

Key Responsibilities:

1. Lead global project teams through the PoC phase, driving the implementation of the PoC strategy; participate in project teams throughout the program lifecycle from NTRC to registration.
2. Responsible for the clinical portions of the Integrated Development Plan (IDP) through PoC.
3. Act as medical monitor for one or more clinical studies.
4. Communicate clinical team matters to project teams and relevant decision boards (Disease Area Decision Board).
5. Convene relevant internal and external leaders to consider proposed approaches to PoC.
6. Evaluate clinical centers and foster communication with key investigators.
7. Oversee publication and external presentation of PoC clinical study results.
8. Accountable for compound-related biomarker strategies; work closely with biomarker experts to implement these strategies.
9. Collaborate with research scientists to identify, develop, and implement strategies for preclinical support of program objectives, including assessment of medical needs, clinical development pathways, and review of preclinical data for clinical implications.
10. Participate in team presentations to Health Authorities as a TM Expert.

Essential Requirements:

• Doctoral degree, MD required, with clinical subspecialty training preferred in cardiovascular disease or endocrinology/metabolic disease; additional PhD or post-doctoral research experience is a plus.
• At least 1-2 years of experience in a pharmaceutical/biotech company, CRO, or academic medical center; 5+ years for consideration at the Director level.
• Recognized medical expertise and scientific contributions, including publications in international journals.
• Excellent written and oral communication skills.
• Ability to work independently on study planning and execution, with supervision on project planning.
• Leadership skills to lead multidisciplinary teams in a matrix organization.
• Innovative mindset to seek new clinical discovery opportunities and PoC approaches.
• Additional experience in data science, genetics/genomics, AI, or digital methods related to cardiovascular imaging or electrocardiography is a plus.
• A demonstrated passion for science.

This is a dual-level posting. The final level and title will be determined based on skills, experience, and capabilities.

Compensation and Benefits:

The pay range at commencement is expected to be between $204,400 and $379,600 at the Associate Director level, and between $236,600 and $439,400 at the Director level. Salary adjustments may occur based on market conditions, experience, and other factors. The total compensation may include bonuses, stock units, and other benefits, including medical, financial, and paid time off benefits. Details will be provided upon offer.

EEO Statement:

Novartis is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other protected status.

Accessibility and Accommodations:

We are committed to providing reasonable accommodations for individuals with disabilities. Contact us at [e-mail] or call [phone] with your request and contact information, including the job requisition number.

Salary Range: $204,400 - $379,600

Skills Desired: Clinical Trials, Data Analysis, Data Monitoring, Drug Development, Drug Discovery, Medical Strategy, People Management