Director, Clinical Science – Hematology Trials Leader

SystImmune, Inc.; Princeton (NJ); On-site; USD 180,000 - 245,000; Full time

Benefits offered by this job

Premium healthcare

STD

LTD

401(k) match

PTO 15 days

Holidays

Job summary

SystImmune, Inc. is seeking a seasoned clinical development professional to drive strategy for assigned trials and contribute to regulatory submissions.

You will author core documents with the Medical Director and lead medical data review, ensuring high-quality data interpretation across hematology programs. Key responsibilities include developing eCRF guidelines, coordinating with KOLs, and preparing materials for investigator meetings and publications.

Qualifications

• Bachelor’s degree in life sciences or health-related field required.
• Advanced degree preferred; therapeutic/clinical science focus beneficial.

Responsibilities

• Contributes to developing the program strategy for assigned trials/compounds.
• Author components with Medical Director for regulatory documents to support registration and commercialization.
• Develops eCRFs and completion guidelines, supporting data management deliverables.
• Lead the development of medical data review and monitoring plans; summarize efficacy and safety data.
• Provide input for country/site selection and feasibility assessment; interact with KOLs.
• Prepare charters and coordinate committee meetings with senior leadership.
• Participate in study plans and liaise with project teams.
• Prepare Investigator meeting presentations and training materials.
• Support publications in coordination with Scientific Communications.

Skills

Data review & interpretation

ICH & GCP knowledge

Scientific communication

Cross-functional collaboration

KOL interaction

Presentations

Education

Bachelor’s degree in life sciences or health-related field

Advanced degree (Masters/PhD/PharmD/MD)

Job description

SystImmune, Inc. is seeking a seasoned clinical development professional to drive strategy for assigned trials and contribute to regulatory submissions.

You will author core documents with the Medical Director and lead medical data review, ensuring high-quality data interpretation across hematology programs. Key responsibilities include developing eCRF guidelines, coordinating with KOLs, and preparing materials for investigator meetings and publications.