Clinical Development Scientist
ARTBIO
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- Location
- Cambridge, MA
- Work style
- Hybrid
- Job type
- Full time
- Posted
- Oct 26
- 4 days ago
Career path
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About the company
ARTBIO
Biotechnology · 11 to 50 employees
What you'll do
- Act as the day-to-day clinical lead for a Radioligand Therapy development program
- Design and author the protocol
- Chair the study team
- Drive the timeline
- Turn emerging clinical data into decisions that advance the asset
What you need
- Advanced degree (MSc, PhD, PharmD, MD or equivalent) in life sciences, pharmacy, medicine or a closely related discipline. Minimum 4 years of clinical development experience for appointment. Experience may be gained in industry or at a CRO and must include hands-on responsibility for at least one oncology study. Demonstrated protocol authoring, including at least one protocol taken from concept through to approval. Hands-on experience of clinical data review, query resolution, and preparation of data packages for safety or dose-escalation committees. Experience with early-phase oncology trial design, including dose escalation, DLT definition and cohort expansion. Ability to read and interrogate imaging, dosimetry, pharmacokinetic and biomarker data.
Key skills
Scientific ownershipProject managementDriving the timelineClinical data
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Summary
We are seeking a Clinical Development Scientist to act as the day-to-day clinical lead for one of ARTBIO's Radioligand Therapy (RLT) development programs, combining scientific ownership of the study with hands-on project management of its execution. Reporting to the VP, Clinical Development and working closely with functional heads and subject matter experts, you will be the person who holds the program together: designing and authoring the protocol, chairing the study team, driving the timeline, and turning emerging clinical data into the decisions that advance the asset.