Clinical Scientist Associate Director at Jobgether – United States

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Scientist Associate Director in the United States.

This role plays a critical part in the execution of late-stage cardiovascular clinical trials, ensuring scientific rigor, operational excellence, and high-quality data delivery across global studies.
You will act as a key clinical development expert, translating scientific strategy into actionable study execution plans that guide complex, event-driven trials.
Working at the intersection of clinical science, operations, and regulatory compliance, you will support cross-functional teams in delivering decision-ready data.
The environment is highly collaborative and science-driven, with strong engagement across medical, safety, data management, and regulatory functions.
You will contribute directly to protocol development, endpoint strategy, and ongoing medical and scientific data review.
This position offers high visibility within global clinical programs and a meaningful impact on cardiovascular drug development.
Overall, you will help ensure clinical trials are executed with precision, integrity, and alignment to regulatory and scientific standards.

• Serve as a clinical and scientific subject matter expert for cardiovascular clinical trials, supporting protocol design, execution, and interpretation.
• Contribute to medical monitoring activities, including review of subject-level and aggregate data to identify safety signals, trends, and risks.
• Support development of key clinical documents such as protocols, endpoint definitions, data review plans, and study charters.
• Ensure scientific and operational integrity of global late-stage clinical trials, particularly event-driven cardiovascular studies.
• Lead clinical data review activities to ensure accuracy, consistency, and compliance with protocol and regulatory requirements.
• Collaborate cross-functionally with clinical operations, data management, safety, and regulatory teams to resolve study issues.
• Provide input into study startup, enrollment strategy, endpoint adjudication, and ongoing trial conduct.
• Support inspection readiness and data quality assessments to ensure high standards throughout the clinical lifecycle.
• Participate in interpretation of study results and preparation of scientific outputs, including publications and regulatory submissions.

Requirements:

• Advanced degree in life sciences or clinical field (PhD, MD, PharmD, Master’s, Bachelor’s, or equivalent experience with progressive clinical science responsibility).
• 3+ years of pharmaceutical clinical development experience for advanced degrees, or equivalent progressive experience in clinical science roles.
• Strong experience supporting late-stage global clinical trials, preferably in cardiovascular or outcomes-based studies.
• Deep understanding of clinical trial design, execution, Good Clinical Practice (GCP), and regulatory expectations.
• Experience with clinical data review, endpoint evaluation, and medical monitoring activities.
• Ability to interpret complex clinical data and translate findings into actionable scientific and operational insights.
• Strong communication and presentation skills for both technical and non-technical audiences.
• Experience collaborating across cross-functional teams in a highly regulated environment.
• Familiarity with clinical data tools and visualization platforms (e.g., Spotfire or equivalent).
• Experience contributing to regulatory documents, publications, or scientific congress materials is a plus.

Benefits:

• Competitive annual salary ranging from approximately $169,793 to $229,721 USD.
• Comprehensive health, dental, and vision insurance for employees and eligible dependents.
• Retirement savings plan with strong employer contributions.
• Annual bonus eligibility and long-term stock-based incentive programs.
• Flexible work models supporting work-life balance where applicable.
• Generous paid time off and award-winning leave programs.
• Career development opportunities within a global, science-driven organization.
• Inclusive and collaborative culture focused on innovation and patient impact.