Director, Clinical Scientist

Kelonia Therapeutics

Clinical Scientist supporting medical monitoring and pharmacovigilance for genetic medicines at Kelonia Therapeutics. Collaborating with cross-functional teams to drive innovative therapies.

Posted 5/5/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesLead💰 $190,000 - $252,000 per yearWebsite

About the role

Key responsibilities & impact

Support day-to-day medical monitoring, clinical development, data services, and pharmacovigilance for lead programs
Collaborate cross-functionally with Clinical Operations, Regulatory, Biometrics, Translational Sciences, and Medical teams to ensure high-quality and timely study execution
Perform ongoing review and interpretation of clinical data, including safety, efficacy, and longitudinal patient data
Act as a primary contributor and owner of key clinical deliverables, including: Clinical study protocols, Investigator’s Brochures, Clinical study reports, and Regulatory submission documents
Support clinical trial conduct and oversight, including data review, issue identification, and resolution
Contribute to regulatory interactions and submissions, including preparation of FDA-facing materials and global regulatory documentation
Partner with Clinical Operations to support patient enrollment strategy and execution

Requirements

What you’ll need

Advanced degree required: PharmD, PhD, or MS in a health or life sciences field
3–6+ years of experience in clinical development within biotech or pharma, preferably in a Clinical Scientist or similar role
Experience in oncology, hematology, and/or cell and gene therapy strongly preferred
Demonstrated experience authoring and contributing to: Clinical protocols and amendments, Investigator’s Brochures, and Regulatory submission documents and clinical datasets
Strong understanding of clinical trial design, execution, and data interpretation
Ability to independently analyze complex clinical data and communicate insights clearly
Comfortable operating in a hands-on, execution-focused role with high ownership of deliverables
Strong cross-functional collaboration skills in a fast-paced, matrixed environment
Experience supporting IND submissions and/or global regulatory activities preferred
Ability and interest to grow into a leadership role as the clinical team expands

Benefits

Comp & perks

Flexible Time Off
Competitive benefits package (health, commuter, and more)
On-site perks including free parking, a state-of-the-art gym, and a food hall

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical developmentdata interpretationclinical trial designclinical protocolsInvestigator’s BrochuresRegulatory submission documentsclinical datasetspharmacovigilanceoncologyhematology

Soft Skills

cross-functional collaborationcommunicationanalytical skillsproblem-solvingownershipleadership potentialexecution-focusedinterpersonal skillsadaptabilityteamwork

Certifications

PharmDPhDMS in health sciencesMS in life sciences