Senior Director, Clinical Research & Trials

Eikon; Jersey City (NJ); Vor Ort; USD 270.000 - 326.000; Vollzeit

Benefits dieser Stelle

401k match

Medical/dental/vision coverage

Mental health benefits

PTO and holidays

Life/AD&D insurance

Parental leave

Lunch on-site

Zusammenfassung

Eikon Therapeutics in Jersey City, NJ seeks a Senior Director, Clinical Research (Medical Director) to lead clinical development studies, providing medical leadership and oversight for oncology and non-oncology programs. The role involves collaborating with cross-functional teams to advance therapies to patients in need.

On-site presence in New Jersey is required a minimum of 3 days per week, with a focus on rigorous scientific quality, regulatory readiness, and timely delivery of study

Qualifikationen

• MD or DO with oncology focus and medical license.
• 5–7 years clinical experience; 3+ years in drug development.
• Experience in clinical trials and medical monitoring.
• In-depth knowledge of GCP and regulatory requirements.
• Ability to work effectively in a matrixed environment.
• Strong communication and cross-functional collaboration.
• IND/NDA/BLA filings preferred.

Aufgaben

• Design and conduct early-stage clinical development trials with safety and efficacy assessment.
• Provide medical monitoring and interpret trial results for regulatory submissions.
• Collaborate with discovery, translational science, toxicology, pharmacology, and regulatory teams.
• Coordinate with Clinical Science, Data Management, Clinical Operations, Biostatistics for integrated execution.
• Address protocol questions from Health Authorities and Ethics Committees consistently.

Kenntnisse

Clinical development

Medical monitoring

Leadership

Oncology experience

Regulatory knowledge

Ausbildung

MD/DO degree

Jobbeschreibung

Eikon Therapeutics in Jersey City, NJ seeks a Senior Director, Clinical Research (Medical Director) to lead clinical development studies, providing medical leadership and oversight for oncology and non-oncology programs. The role involves collaborating with cross-functional teams to advance therapies to patients in need.

On-site presence in New Jersey is required a minimum of 3 days per week, with a focus on rigorous scientific quality, regulatory readiness, and timely delivery of study