Scientific Writer - Entry Level

Description

1. Home
2. Search Jobs
3. Job Description

Scientific Writer - Entry Level

Contract: Irvine, California, US

Salary Range: 30.00 - 35.00 | Per Hour

Job Code: 369647

End Date: 2026-06-25
Days Left: 22 days, 3 hours left

Apply

To Discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL ), email your updated resume at Email View email address on click.appcast.io . Thank you!

*]:pointer-events-auto R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]" dir="auto" data-turn-id="request-WEB:9b59a97c-f35a-4664-8948-c986e54e07ff-2" data-turn-id-container="request-WEB:9b59a97c-f35a-4664-8948-c986e54e07ff-2" data-testid="conversation-turn-4" data-scroll-anchor="false" data-turn="assistant">

Pay Range: $30 to $35 an hour.

Client Industry: Pharmaceutical

Job Mode: Onsite

Contract Duration: 6 Months (Possibilities of Extension)

Job Summary:

We are seeking an experienced Scientific Writer to support scientific publication and regulatory documentation activities within a large enterprise environment. This role will focus on preparing high quality scientific documents, publication materials, and regulatory content while ensuring documentation accuracy and compliance. The ideal candidate will collaborate with cross functional teams to support journal submissions, abstracts, posters, and controlled documentation processes. Strong organizational skills and experience managing documentation systems are essential for success in this role. This is an excellent opportunity for professionals with life sciences and regulatory writing expertise.

Key Responsibilities:

• Prepare scientific and regulatory documents for publication and submission activities
• Generate graphs and figures for journal publications and poster presentations
• Manage controlled and non controlled documentation processes
• Maintain publication records and update project tracking systems
• Coordinate with cross functional teams to gather scientific content and documentation
• Support preparation of abstracts, study reports, and posters
• Ensure documentation accuracy, compliance, and version control within internal systems
• Complete additional scientific writing projects as assigned

Required Qualifications:

• Bachelor's degree in Life Sciences, Clinical Laboratory Science, or related field
• Minimum 3 years of scientific writing or regulatory writing experience
• Experience supporting scientific publications and regulatory submissions
• Strong communication and organizational skills
• Experience using SharePoint or similar document management platforms
• Ability to work effectively with multiple teams and departments

Preferred Qualifications:

• Master's degree in Life Sciences or related field
• Experience within pharmaceutical, biotechnology, or medical device environments
• Familiarity with publication planning and scientific communication activities
• Experience working with secure documentation and tracking systems

Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)

Job Requirement

• Scientific Writing
• Regulatory Writing
• Abstracts
• SharePoint
• Documentation Management
• Publication Support
• manuscripts

Reach Out to a Recruiter

• Recruiter
• Email
• Phone
• Deepak Arya
• View email address on click.appcast.io

Apply Now