Clinical Development Lead, Radioligand Therapy

ARTBIO; Cambridge (MA); On-site; USD 180,000 - 260,000; Full time

Benefits offered by this job

Competitive compensation and benefits

Hands-on training and professional dev

International, collaborative culture

Job summary

ARTBIO is seeking a Clinical Development Scientist to serve as the day-to-day clinical lead for an RLT oncology program. You will design protocols, chair the study team, drive timelines, and translate clinical data into decisions to advance the asset.

You will own safety review, data management, and regulatory contributions, while coordinating with Clinical Operations, Finance, and external partners in a fast-paced biotech setting.

Qualifications

• Advanced degree in life sciences, pharmacy, medicine or a closely related discipline.
• Minimum 4 years of clinical development experience with hands-on oncology study responsibility.
• Demonstrated protocol authoring from concept through approval.
• Hands-on clinical data review and data-package preparation for safety or dose-escalation committees.
• Experience with early-phase oncology trial design including dose escalation and cohort expansion.
• Ability to read and interrogate imaging, dosimetry, pharmacokinetic and biomarker data.

Responsibilities

• Design and author clinical study protocols and informed consent forms.
• Chair study team meetings and drive decisions to closure.
• Manage study budget and forecast with Clinical Operations and Finance.
• Oversee ongoing clinical data review and safety data packages.
• Support regulatory content for IND/CTA submissions and DSURs.
• Engage sites, vendors and investigators and manage external relationships.

Skills

Protocol authoring

Clinical data review

Early-phase oncology trial design

Imaging/dosimetry data interpretation

Cross-functional collaboration

Budget & forecast management

Study team facilitation

Education

Advanced degree (MSc/PhD/PharmD/MD) in life sciences or related

Job description

ARTBIO is seeking a Clinical Development Scientist to serve as the day-to-day clinical lead for an RLT oncology program. You will design protocols, chair the study team, drive timelines, and translate clinical data into decisions to advance the asset.

You will own safety review, data management, and regulatory contributions, while coordinating with Clinical Operations, Finance, and external partners in a fast-paced biotech setting.