Senior Director, Clinical Scientist - Oncology Trials

Menarini Group; New York (NY); On-site; USD 215,000 - 275,000; Full time

Benefits offered by this job

Incentive programs

401(k) with company match

Health insurance (PPO/HDHP)

Life & AD&D insurance

Pre-tax FSA/HSA

Job summary

Menarini Stemline seeks a Clinical Scientist (Director/Senior Director) to lead and execute oncology clinical development programs. You will partner with Medical Directors to shape study design, data interpretation, and regulatory submissions, while guiding cross-functional teams in a matrix environment.

The role includes collaboration with KOLs, site training, and presenting data at conferences. Domestic and international travel may be required, with ETZ hours and a competitive compensation

Qualifications

• 5+ years’ experience in drug development as a clinical scientist or related role in pharmaceutical/biotech industry.
• Advanced degree (e.g. MS, PharmD, PhD) or equivalent experience is required
• Experience in late phase solid tumor oncology is required.
• Proficient with Microsoft Word/Excel/PowerPoint, EDC systems (e.g. Medidata RAVE), and data review tools
• Knowledge of GCP, ICH Guidelines and current US FDA regulations.

Responsibilities

• Plan, execute, and report clinical trials, primarily in oncology.
• Contribute to study documents and regulatory submissions (protocols, ICFs, CSRs).
• Collaborate with external partners and cross-functional teams; oversee study committees.
• Develop and present training materials and study data results to internal and external audiences.
• Support trial operations and data collection aligned with the protocol.

Skills

Clinical development

Oncology expertise

Data interpretation

Regulatory awareness

Cross-functional collaboration

Education

Advanced degree (MS/PhD/PharmD)

Tools

Medidata RAVE (EDC)

MS Office (Word/Excel/PowerPoint)

Job description

Menarini Stemline seeks a Clinical Scientist (Director/Senior Director) to lead and execute oncology clinical development programs. You will partner with Medical Directors to shape study design, data interpretation, and regulatory submissions, while guiding cross-functional teams in a matrix environment.

The role includes collaboration with KOLs, site training, and presenting data at conferences. Domestic and international travel may be required, with ETZ hours and a competitive compensation