Scientific Writer II, Preclinical Research

Position: Scientific Writer II Preclinical Research

Pay Range: $60k - $75k

Location: Carlsbad CA (On-site)

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25000 employees worldwide across 28 locations in the US UK China and Singapore we support drug discovery through to manufacturing with fully integrated high-quality services.

Were proud of the impact we make and just last year we supported 887 discovery projects 1100 CMC programs and 1397 clinical trials across all phases. Our teams are involved in everything from small molecules ADCs biologics and gene therapies and we work with more than 3300 global customers. To learn more visit .

What Youll Do

Join Pharmarons Preclinical Research team as a Scientific Writer II where youll play a critical role in preparing high-quality nonclinical study protocols reports and scientific documentation supporting pharmaceutical and medical device research. Working closely with Study Directors and multidisciplinary scientific teams youll translate complex preclinical study data into clear accurate and GLP-compliant documentation that supports the successful execution and reporting of nonclinical studies.

The ideal candidate is a detail-oriented scientific writer with experience supporting preclinical research who enjoys transforming complex scientific findings into well-organized regulatory-compliant reports. This is an excellent opportunity to contribute to a diverse portfolio of nonclinical studies while working in a collaborative fast-paced CRO environment.

Key Responsibilities

• Partner with multidisciplinary scientific teams to develop review and finalize nonclinical study protocols reports and scientific documentation supporting pharmaceutical and medical device development.
• Translate complex scientific data into clear concise and scientifically accurate protocols study reports summaries and regulatory documentation.
• Prepare publication-quality tables figures graphs and data visualizations that effectively communicate study results and scientific conclusions.
• Provide scientific writing guidance editorial support and standardized language to ensure clarity consistency and scientific accuracy across all documentation.
• Ensure documentation complies with GLP regulations sponsor requirements company standards and applicable regulatory guidelines.
• Collaborate with Study Directors scientists Quality Assurance and cross-functional teams to ensure timely completion of study documentation.
• Assist in the development and maintenance of protocol report and template libraries within Provantis.
• Generate statistical tables and apply appropriate reporting tools using Provantis.
• Contribute to continuous process improvement through the development and revision of SOPs templates and scientific writing best practices.
• Mentor and provide technical guidance to Assistant Scientific Writers and Scientific Writer I team members.
• Manage multiple writing projects simultaneously while meeting established study timelines.

What Were Looking For

• Bachelors Masters or Ph.D. degree in Life Sciences Pharmaceutical Sciences Pharmacology Toxicology Biology or a related scientific discipline.
• Bachelors degree with 3 years Masters degree with 2 years or Ph.D. with relevant industry experience in scientific writing preclinical research or a related scientific field.
• Experience authoring or reviewing nonclinical protocols study reports or regulatory documentation within a CRO pharmaceutical biotechnology or medical device environment.
• Strong understanding of preclinical drug development GLP studies and scientific documentation supporting pharmaceutical or medical device programs.
• Experience working in a GLP-regulated environment is strongly preferred.
• Experience using Provantis or similar electronic data management and reporting systems is preferred.
• Exceptional scientific writing technical editing and document review skills with meticulous attention to detail.
• Demonstrated ability to interpret complex scientific data and communicate findings clearly and accurately.

Why Pharmaron

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004 Pharmaron has invested in its people and facilities and established a broad spectrum of research development and manufacturing service capabilities throughout the entire drug discovery preclinical and clinical development process across multiple therapeutic modalities including small molecules biologics and CGT products. With over 25000 employees and operations in the US UK China and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America Europe Japan and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment where teamwork and innovation go hand in hand. Here your voice matters and your contributions make a real impact. Employees Number One and Clients Centered are the core cultural values at Pharmaron. Our culture which sets Pharmaron apart from other organizations has evolved from our deep commitment to our employees partners and collaborators.

Benefits: As part of our commitment to your well-being we offer a comprehensive benefits package:

• Comprehensive Medical Dental & Vision Insurance with significant employer contributions
• 401(k) Retirement Plan with generous employer matching
• Generous Paid Time Off (PTO) Paid Sick Leave & Company Holidays to support work-life balance
• Employer-funded Health Savings Account (HSA) contributions (for eligible plans) plus Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life Insurance AD&D Short- and Long-Term Disability Insurance
• Employee Assistance Program (EAP) mental health resources and wellness programs
• Family-friendly benefits including fertility support and maternity resources
• Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:

Ready to seize this incredible opportunity Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer Pharmaron values diversity and inclusion in the workplace fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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