Associate Director, Clinical Sciences & Study Design

Isbjørn Is; Cambridge, Northern (MA, KY); Hybrid; USD 150,000 - 190,000; Full time

Job summary

Hemab Therapeutics in Cambridge, MA is seeking an Associate Director, Clinical Sciences to translate science into well‑designed clinical studies and reliable evidence about how our treatments perform in patients.

You'll lead protocol development, study execution and data review with Medical Directors, guiding sites and vendors to ensure trials run as intended across two hubs and multiple time zones.

Qualifications

• Significant experience in clinical science or clinical research within drug development.
• Experience developing clinical protocols and reviewing clinical study data.
• Strong working understanding of ICH-GCP and regulated drug development.
• Ability to interpret clinical information and apply it to development decisions.

Responsibilities

• Drive clinical science contribution to study design and execution.
• Lead protocol development with Medical Director and amendments as needed.
• Review study data, identify safety/efficacy trends needing action.
• Develop study documents (informed consent forms, eCRFs, monitoring plans).
• Guide sites and vendors on protocol requirements and participant management.
• Help communicate findings to internal and external stakeholders.

Skills

Clinical sciences

Clinical research

Study design

ICH-GCP

Data interpretation

Cross-functional collaboration

Education

Advanced scientific or clinical degree

Job description

Hemab Therapeutics in Cambridge, MA is seeking an Associate Director, Clinical Sciences to translate science into well‑designed clinical studies and reliable evidence about how our treatments perform in patients.

You'll lead protocol development, study execution and data review with Medical Directors, guiding sites and vendors to ensure trials run as intended across two hubs and multiple time zones.