Lead, Hematology-Oncology Clinical Development

Jobtailor; New Jersey; On-site; USD 180,000 - 240,000; Full time

Job summary

Jobtailor in New Jersey is seeking a physician-lead to drive clinical strategy and oversight across a major program. You will guide Clinical Scientists and Operations staff, ensuring alignment with global development standards and regulatory expectations.

You will interact with regulators and key opinion leaders, steering program direction and contributing to SOP creation. Strong collaboration with Research, Medical Affairs, and other functions is essential.

Qualifications

• MD or equivalent medical degree with clinical Residency training.
• Hematology or Oncology fellowship training strongly preferred.
• More than 2 years of experience in clinical research or drug development across Phases I–IV.
• Medical/scientific expertise in hematologic malignancies preferred.

Responsibilities

• Lead clinical strategy and deliverables for an assigned section of a clinical program.
• Drive execution across trial phases in partnership with global line functions.
• Guide and support assigned Clinical Scientists and Clinical Operations associates.
• Represent the program in interactions with regulatory authorities, key opinion leaders, and advisory boards.
• Partner cross-functionally with Research, Early Clinical Development, Medical Affairs, Marketing, and HE&OR.
• Contribute to internal decision boards shaping program direction.
• Shape Global Clinical Development standards by authoring or reviewing SOPs.
• Participate in training programs and strategic taskforces that advance clinical development practices.

Skills

Clinical strategy development

Trial phase execution

SOP drafting and reviewing

Cross-functional collaboration

Regulatory interactions

Education

MD or equivalent medical degree

Clinical Residency training

Hematology or Oncology fellowship

Job description

Jobtailor in New Jersey is seeking a physician-lead to drive clinical strategy and oversight across a major program. You will guide Clinical Scientists and Operations staff, ensuring alignment with global development standards and regulatory expectations.

You will interact with regulators and key opinion leaders, steering program direction and contributing to SOP creation. Strong collaboration with Research, Medical Affairs, and other functions is essential.