Senior Director, Clinical Research, Atherosclerosis

Job Description

The Senior Director (Sr. Principal Scientist) is responsible for planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The role manages the entire cycle of late‑stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.

• Planning clinical trials (design, operational plans, settings) based on clinical development strategies.
• Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Atherosclerosis drugs.
• Analyzing and summarizing clinical findings to support safety, efficacy decisions, new drug applications, clinical study reports, and publications.
• Participating in internal and joint research project teams relevant to new and existing compounds.
• Evaluating pre‑clinical and translational work to generate early clinical development plans and Investigational New Drug (IND) applications.
• Developing clinical development strategies for investigational or marketed Atherosclerosis drugs.
• Supporting business development assessments of external opportunities.
• Working closely with Clinical Scientists and cross‑functional groups (commercialization, regulatory affairs, statistics, manufacturing) to manage clinical development projects.
• Maintaining a strong scientific knowledge base through awareness of new findings and research methodologies.
• Identifying and establishing relationships with qualified investigators to assist in the evaluation of company drugs.
• Attending scientific meetings to maintain competency and stay informed on research activities.
• Authoring detailed development documents, presentations, budgets, and position papers for internal and external audiences.
• Facilitating collaborations with external researchers worldwide.
• Traveling on company business, approximately 20–25% of the time, to manage ongoing or future clinical research projects.

• M.D. or M.D./Ph.D.

• Experience in industry or as senior faculty in academia.
• Minimum of 3 years experience in clinical medicine.
• Minimum of 3–5 years industry experience in drug development or equivalent academic biomedical research experience.
• Demonstrated success in overseeing Phase 2 and Phase 3 clinical studies and protocols.
• Demonstrated record of scientific scholarship and achievement.
• Proven track record in clinical medicine and background in biomedical research.
• Strong interpersonal skills and ability to work effectively in a team environment.
• Outstanding verbal and written communication and presentation skills.

• Board Certified or Eligible in Cardiology (adult or pediatric), Endocrinology, Nephrology, or a related discipline.
• Prior specific experience in clinical research and prior publication.

• Atherosclerosis
• Cardiovascular Diseases
• Clinical Development
• Clinical Research
• Clinical Sciences
• Clinical Trials
• Cross‑Functional Teamwork
• Drug Development
• Medical Monitoring
• Scientific Writing

• Current employees apply HERE
• Current contingent workers apply HERE

25% of the time.

Hybrid.

Salary range: $ – $. To be determined based on experience. Eligible for annual bonus and long‑term incentive, if applicable. The company offers a comprehensive benefits package including medical, dental, vision, healthcare, retirement benefits (401(k)), paid holidays, vacation, and compassionate and sick days.

As an Equal Employment Opportunity Employer, we provide equal opportunities for all employees and applicants and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability status, or any other legally protected characteristics.