Medical Director

Scorpion Therapeutics; Boston (MA); On-site; USD 230,000 - 320,000; Full time

Job summary

Scorpion Therapeutics in the Boston area seeks a Medical Director to oversee clinical and medical initiatives for oncology assets, reporting to the Chief Medical Officer. The role covers early to late-stage development, including antibody modalities.

On-site in Brighton, MA with a 4-day/week onsite expectation. You will lead clinical research activities, manage CRO relationships, monitor trial progress, oversee data and safety activities, and collaborate with clinical operations and

Qualifications

• MD with oncology or immuno-oncology background.
• Minimum 5+ years in the pharmaceutical industry.
• Extensive clinical trial and drug development experience.
• Deep understanding of regulatory guidelines (FDA, cGCP).
• Strong communication and mentoring abilities.

Responsibilities

• Ensure milestone achievement within quality and regulatory standards.
• Lead clinical research activities.
• Manage CRO relationships.
• Monitor trial progress.
• Oversee data and safety activities.
• Collaborate with clinical operations and cross-functional teams.
• Develop external KOL relationships.
• Evaluate clinical data for efficacy and safety.

Skills

MD with oncology/IO background

5+ years in industry

FDA & cGCP regulatory knowledge

Strong communication

Mentoring ability

Education

MD in Oncology or IO

Job description

Role

Medical Director overseeing clinical and medical initiatives for early to late-stage oncology assets, including antibodies, reporting to the Chief Medical Officer.

Responsibilities

• ensure milestone achievement within quality and regulatory standards


• lead clinical research activities


• manage CRO relationships


• monitor trial progress


• oversee data and safety activities


• collaborate with clinical operations and cross-functional teams


• develop external KOL relationships


• evaluate clinical data for efficacy and safety.

Qualifications

• MD with oncology or immuno-oncology background


• 5+ years in industry


• extensive clinical trial and drug development experience


• deep understanding of regulatory guidelines (FDA, cGCP)


• strong communication skills


• ability to mentor.

HighValue

• oncology


• immuno-oncology


• antibody modalities


• clinical development from early to late phases


• regulatory oversight


• GxP compliance


• stakeholder collaboration.

WorkSetup

on-site in Brighton, MA, with a 4-day/week onsite expectation.