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Scientific Writer Job at Pharmaron USA | Biology Apply now

Scientific Writer – Preclinical Ocular Services role at Pharmaron USA

Pharmaron is hiring a scientific writer for its Preclinical Ocular Services team in Carlsbad, CA. This scientific writer job offers the opportunity to draft high-quality nonclinical study protocols and reports that support regulatory submissions and preclinical development milestones in a collaborative and innovative environment. Explore offers similar to Scientific Writer job offer.

Job Details:

  • Position: Scientific Writer – Preclinical Ocular Services
  • Location: Carlsbad, CA (On-site)
  • Salary: $65,000 – $75,000 per year
  • Job Type: Full-Time
  • Experience Required: Minimum 2+ years in pharmaceuticals, CRO, biotech, medical devices, or academic research

About Pharmaron:

Pharmaron is a leading global Contract Research Organization (CRO) supporting pharma and biotech companies in bringing new therapies to life. With over 21,000 employees across 23 locations in the US, UK, and China, Pharmaron provides fully integrated services from drug discovery to manufacturing. Last year, Pharmaron supported 780+ discovery projects, 1,000+ CMC programs, and 1,000+ clinical trials across all phases, serving more than 3,000 global clients.

Educational Requirements:

  • Bachelor’s degree in Biology, Anatomy, Animal Science, or related scientific field.
  • Minimum 2+ years of relevant industry experience preferred.

Key Responsibilities for Scientific Writer role:

  • Draft, revise, and finalize nonclinical study protocols and reports with scientific teams.
  • Prepare written summaries and data tables according to internal templates and sponsor guidelines.
  • Perform editorial review for clarity, accuracy, and regulatory compliance.
  • Verify data and crosscheck documents for completeness.
  • Translate complex scientific information into concise, high-quality content.
  • Collaborate effectively with multidisciplinary teams and manage changing priorities.
  • Communicate proactively with scientific, operational, and project stakeholders.
  • Support additional scientific writing and documentation needs as assigned.

Skills Required for Scientific Writer role:

  • Strong scientific writing and data interpretation skills.
  • Understanding of drug development and preclinical study requirements.
  • Excellent attention to detail and organizational abilities.
  • Proficiency in written and verbal English communication.
  • Prior experience drafting nonclinical study protocols or reports is highly preferred.

Benefits of the Role:

  • Comprehensive insurance including Medical, Dental & Vision with employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to Employee Assistance Program
  • Inclusive and collaborative culture valuing employee contributions

CLICK HERE TO APPLY

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