Associate Director of Cardiovascular Division

Essen Medical Associates•New York, NY

3d•Hybrid

About The Position

The Associate Director (AD) of the Cardiovascular Division provides strategic, operational, and scientific leadership to support the development, launch, and lifecycle management of cardiovascular products or programs. This role partners cross-functionally to ensure alignment with clinical, regulatory, commercial, and medical objectives while maintaining the highest standards of scientific integrity, compliance, and patient focus.

Requirements

Advanced degree preferred: MD, PharmD, PhD, or equivalent in a life science or medical discipline.
Relevant bachelor’s or master’s degree with significant experience may be considered.
7–10+ years of experience in cardiovascular medicine within pharma, biotech, medical affairs, clinical research, or related fields.
Demonstrated experience working cross-functionally in a matrix environment.
Prior leadership or project-management experience preferred.
Strong knowledge of cardiovascular disease areas and therapeutic landscapes.
Excellent strategic thinking, analytical, and problem-solving skills.
Strong communication and presentation abilities.
Ability to influence without authority and work effectively across functions.
High level of professionalism, integrity, and attention to detail.

Nice To Haves

Experience supporting product launches or late-stage development programs.
Exposure to global or regional cardiovascular strategies.
Strong relationships with cardiovascular KOLs or professional societies.

Responsibilities

Contribute to and execute the cardiovascular division’s short- and long-term strategy.
Support portfolio planning, indication expansion, and lifecycle management initiatives.
Analyze competitive landscape and emerging trends in cardiovascular medicine.
Provide subject-matter expertise in cardiovascular disease areas (e.g., heart failure, hypertension, dyslipidemia, arrhythmias).
Review and contribute to clinical trial protocols, study reports, and publications.
Support interactions with key opinion leaders (KOLs), investigators, and advisory boards.
Partner with Clinical Development, Regulatory Affairs, Commercial, Market Access, and Pharmacovigilance teams.
Ensure alignment of medical strategy with commercial objectives while maintaining compliance.
Support global and regional team coordination as needed.
Lead or support cardiovascular projects, ensuring timelines, budgets, and deliverables are met.
Oversee vendors, CROs, or external partners as applicable.
Contribute to SOP development and process improvement initiatives.
Ensure all activities adhere to internal policies, industry regulations, and ethical standards.
Support regulatory submissions, audits, and inspections as required.
Mentor junior team members and contribute to talent development.
Act as a role model for scientific excellence, collaboration, and accountability.