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Pharmaron · 1 month ago

Scientific Writer – Preclinical Ocular Services

Carlsbad, CA

Full-time

Onsite

Entry, Mid Level

$65K/yr - $75K/yr

2+ years exp

Pharmaron is a global CRO helping pharma and biotech companies bring new therapies to life. They are seeking a Scientific Writer to support their Preclinical Ocular Services group, responsible for drafting and finalizing nonclinical study protocols and reports to support regulatory submissions and preclinical development milestones.

BiotechnologyChemicalPharmaceutical

Responsibilities

Draft, revise, and finalize nonclinical study protocols and reports in collaboration with scientific teams

Prepare written summaries and data tables in compliance with internal templates and sponsor guidelines

Provide editorial review to ensure clarity, consistency, accuracy, and adherence to regulatory and eCTD formatting requirements

Verify data and perform crosschecks to ensure completeness and accuracy of all documents

Translate complex scientific information into concise, high-quality written content

Work effectively within multidisciplinary teams and adapt to shifting timelines and priorities

Communicate clearly and proactively with scientific, operational, and project stakeholders

Support additional scientific writing and documentation needs as assigned

Qualification

Scientific writingDrug development knowledgeNonclinical study protocolsTechnical data interpretationEnglish communicationAttention to detailOrganizational skills