Project Manager, Preclinical Research; Ophthalmology
Listed on 2026-10-23
-
IT/Tech
Information Security & Data Protection, IT Support
Position: Project Manager, Preclinical Research (Ophthalmology)
Salary Range: $70k - $100k
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 25,000 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.
We're proud of the impact we make and just last year, we supported 887 discovery projects
, 1,100+ CMC programs
, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers
. To learn more, visit
What You'll Do
The Project Manager will support complex preclinical ophthalmology programs and serve as a key liaison between clients, scientific teams, and operational leadership.
We are also open to considering candidates at the Associate Project Manager level
, depending on their experience, qualifications, and project management capabilities. The final title and level will be determined based on the selected candidate's background.
This role combines scientific understanding, regulatory awareness, and client-facing communication to ensure the successful execution of ocular and related therapeutic studies. The ideal candidate will support preclinical programs focused on ophthalmology, with exposure to CNS, oncology, or cell and gene therapy (CGT) applications.
Key Responsibilities
- Develop a strong understanding of Pharmaron's ocular testing workflows, including preclinical safety, pharmacology, and biocompatibility assessments.
- Collaborate with scientific teams to align study design, timelines, and deliverables with client expectations.
- Support project execution from initiation through final reporting, ensuring adherence to scope, timeline, and budget.
- Draft detailed study proposals, scopes of work, and budgets in collaboration with scientific leadership and Business Development teams.
- Ensure proposals align with departmental capabilities and regulatory standards.
- Support bid defense preparation and client-facing scientific discussions as needed.
- Serve as a primary point of contact for assigned studies, providing regular updates and responding to client inquiries.
- Facilitate effective communication between internal scientific teams and external sponsors.
- Maintain high-quality documentation ensuring project traceability, compliance, and transparency.
What We're Looking For
- Master's degree preferred in Biology, Neuroscience, Ophthalmology, Pharmacology, or a related life sciences discipline.
- Bachelor's degree with strong relevant experience will be considered.
- 2+ years of experience in a preclinical CRO, biotech, or pharmaceutical environment.
- Hands-on experience supporting in vivo animal research studies is required.
- Prior experience in ophthalmology, ocular research, neuroscience, or CGT programs strongly preferred.
- Demonstrated experience supporting study proposals, budgets, or client-facing scientific interactions is a plus.
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 25,000 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…
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