Top 2613 Manager, regulatory affairs Jobs in Oceanside Ca

Project Manager / Senior Project Manager – Nonclinical Antiviral Development (NIAID Funded Program)
Arisan Therapeutics, Inc —Carlsbad, CA
- $145,000 - $189,000 a year
- Full-time
- Background check
- 7 years
- Project management
- Paid holidays
- Relocation assistance
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K-8 Teacher / Classroom Manager - Vista USD, CA - $22-40/hr - Open Schedule Afterschool
Kodely —Vista, CA
- $22 - $40 an hour
- Part-time
- School experience
- Classroom
- Clean driving record
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6d
Community Association Manager
HOA Community —Temecula, CA
- $75,000 - $90,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Customer service
- Health savings account
- Health insurance
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Senior Revenue Cycle Manager
The Neurology Center —Carlsbad, CA
- $80,000 - $100,000 a year
- Full-time
- Background check
- 7 years
- Microsoft Excel
- Health insurance
- Dental insurance
Quick Apply
2d
Project Manager
Aerospace and Defense Manufacturing Inc —Temecula, CA
- $75,000 - $115,000 a year
- Full-time
- Mid-level
- Office
- High school diploma or GED
- Health savings account
- Paid holidays
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18h
Vendor Manager
Ream Franchise Group —Carlsbad, CA
- $95,000 - $140,000 a year
- Full-time
- Microsoft Excel
- 5 years
- Urgent Care
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Director, Regulatory Affairs
Mapp Biopharmaceutical —San Diego, CA
- $130,000 - $250,000 a year
- Full-time
- Remote
- 5 years
- Bachelor's degree
- Product management
- Paid holidays
- Disability insurance
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Inside Sales Representative - Wholesaling (No License) - All Inbound Leads
Buying Americas Homes —Carlsbad, CA
- $91,000 - $135,000 a year
- 8 hour shift
- Sales
- Customer service
- English
- Paid training
- Paid time off
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Sr. Manager, Technical Program Management, Experience Team
ServiceNow —San Diego, CA
- $171,900 - $300,800 a year
- Online Application
- 6 years
- Bachelor of Science
- Residential
- Employee stock purchase plan
- Health insurance
Quick Apply
9d
Manager, Regulatory Affairs
Grifols —Vista, CA
- $131,363 - $197,046 a year
- Full-time
- Hybrid work
- Microsoft Excel
- 5 years
- Bachelor's degree
- Paid holidays
- Health insurance
1d
Client Relationship Manager, Employee Group Benefits - Los Angeles or San Diego, CA
The Hartford —Carlsbad, CA
- $80,000 - $120,000 a year
- Full-time
- Hybrid work
- Microsoft Outlook
- Mid-level
- Office
- Disability insurance
Manager, Customer Service Repairs and Returns | Titleist
Acushnet Golf —Carlsbad, CA
- $101,727 - $129,537 a year
- Full-time
- 5 years
- High school diploma or GED
- Analysis skills
- Health savings account
- Flexible spending account
7d
Manager, Clinic Ops - Family Practice - Jefferson Clinic
Scripps Health —Oceanside, CA
- $49.21 - $71.34 an hour
- Full-time
- Internal Medicine
- High school diploma or GED
- Clinic
6d
ADMINISTRATIVE SERVICES MANAGER
City of San Marcos, California —San Marcos, CA
- $124,487.70 - $172,268.02 a year
- Full-time
- Customer service
- Office
- Administrative experience
Public Affairs Manager, Southern California
Flock —Temecula, CA
- $130,000 - $170,000 a year
- Email
- Remote
- Writing skills
- Mid-level
- Travel
- Paid parental leave
- Health savings account
Senior Manager Talent Development & Engagement
TaylorMade Golf Company —Carlsbad, CA
- $140,000 - $155,000 a year
- Extended hours
- Microsoft Excel
- Microsoft Outlook
- Office
- Paid holidays
- Health insurance
Workplace Manager
Rockstar Games —Carlsbad, CA
- $97,500 - $136,500 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Sanitation
Quick Apply
Program Manager, Healthcare
Kellermeyer Bergensons Services —Oceanside, CA
- $130,000 - $160,000 a year
- Weekends as needed
- Remote
- OSHA
- 5 years
- Bachelor's degree
Quick Apply
Sr. Manager, Talent Management
Thermo Fisher Scientific —Carlsbad, CA
- $130,000 - $194,950 a year
- Full-time
- Office
- Analysis skills
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Regulatory Affairs Manager
ORIC Pharmaceuticals —San Diego, CA
- $145,000 - $165,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Bachelor's degree
- Senior level
Quick Apply

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Project Manager / Senior Project Manager – Nonclinical Antiviral Development (NIAID Funded Program)

Arisan Therapeutics, Inc
Carlsbad, CA

Quick Apply

Job Details

Full-time
$145,000 - $189,000 a year

Benefits

Stock options
Paid holidays
Relocation assistance
Health insurance
401(k)
Paid time off
401(k) matching

Qualifications

Project development phase management
Teamwork
Managing healthcare project budgets
DoD experience
Contract management experience in healthcare
Schedule management
Product development projects
Project management
Bachelor's degree
Pharmaceutical company experience
Project task coordination
Virology
Organizational skills
Contracts
Chemistry, manufacturing & controls
Managing projects
Toxicology
Budgeting
Project contract management
Pharmaceutical research experience
Project stakeholder communication
Cross-functional communication
Stakeholder management

Full Job Description

Project Manager / Senior Project Manager – Nonclinical Antiviral Development (NIAID‑Funded Program)

We are a small, science‑driven biopharmaceutical company located in Carlsbad, CA, advancing first‑in‑class preclinical and Phase 2 clinical development programs primarily through U.S. government‑funded support. We operate with the agility of a startup and the rigor required for global regulatory success. Every team member plays a direct role in shaping the program and accelerating delivery of urgently needed antiviral therapies.

Position Summary

We are seeking an experienced, highly organized full-time, on-site Project Manager to lead a nonclinical antiviral development program from post-discovery through Phase 1. This individual will serve as the operational hub for a cross-functional team spanning nonclinical, CMC, regulatory, and external partners. The ideal candidate brings hands-on experience managing government-funded drug development contracts—preferably with NIH/NIAID, BARDA, or the Department of Defense—and understands the unique reporting, compliance, and milestone-driven expectations of government agencies. Additional pluses would include experience with antiviral or infectious disease programs, including advanced animal efficacy models and coordinating NIAID DMID-funded testing or development networks, as well as familiarity with IND-enabling requirements and early clinical development

This role is perfect for someone who thrives in a small‑company environment, enjoys building structure where needed, and can drive execution across multiple technical workstreams.

Key Responsibilities

Program Leadership & Execution

· Lead day-to-day project management for a small‑molecule antiviral program from post-discovery through IND and Phase 1.

· Develop and maintain integrated project plans, timelines, budgets, and risk registers.

· Drive cross-functional alignment across nonclinical, CMC, regulatory, and external collaborators.

· Ensure timely execution of studies supporting IND‑enabling packages (toxicology, safety pharmacology, ADME, virology, formulation, and manufacturing).

· Operate within a government contract framework, ensuring compliance with government contractual requirements.

Government Contract Management

· Manage contract deliverables, reporting requirements, milestone documentation, and compliance obligations.

· Serve as primary operational liaison with NIAID DMID program staff and technical teams.

· Coordinate government-funded testing through NIAID/NIH networks (e.g., antiviral screening, animal models, PK/PD studies).

· Ensure alignment with FDA study compliance and expectations for documentation, transparency, and audit readiness.

Vendor & CRO Oversight

· Manage relationships with CROs, CDMOs, academic collaborators, and government testing facilities.

· Support study initiation, execution, and delivery of high-quality data packages.

· Track performance, budgets, and timelines; escalate risks proactively.

Regulatory & NDA Support

· Partner with Regulatory Affairs to support NDA planning, data QC, cross‑functional readiness, and submission execution.

· Coordinate preparation for regulatory meetings (e.g., pre‑IND, IND, and End‑of‑Phase 1).

· Ensure nonclinical, CMC, and clinical data packages are delivered on time and in compliance with contractual and global regulatory expectations.

Communication & Reporting

· Prepare and lead internal and external project updates, dashboards, and risk assessments with internal team members and government and other project stakeholders.

· Serve as a liaison with the government and other project stakeholders.

· Lead regular team meetings, ensuring clear action items and accountability.

· Deliver high‑quality written reports and presentations for government agencies and internal leadership.

Qualifications

Required

· Bachelor’s degree in life sciences, engineering, or related medical field

· 7+ years of project management experience in biotech/CRO/pharma.

· Demonstrated experience managing biopharma or government-funded (NIH/NIAID, BARDA, DoD, or similar) drug development preclinical and/or clinical contracts .

· Strong understanding of nonclinical development workflows (toxicology, pharmacology, ADME, virology, CMC).

· Proven ability to manage complex timelines, budgets, and multi-partner programs.

· Exceptional communication, organization, and stakeholder‑management skills.

· Comfortable working in a small, fast‑moving, resource‑lean environment, fostering accountability.

Preferred

· Experience conducting or managing IND-enabling studies and early clinical

· Experience with antiviral or infectious disease programs.

· Experience coordinating NIAID DMID-funded testing or development networks.

What We Offer

· A central leadership role in shaping program strategy and execution through preclinical and IND-enabling studies, and initial human clinical studies in a global health / U.S. defense medical countermeasure program.

· Collaborative, mission-focused culture with scientific rigor and operational agility.

· Competitive salary range of $145,000 – $189,000 based on experience and qualifications.

· Company incentive stock option plan.

· Health insurance coverage.

· 401k retirement savings plan with company matching.

· Paid time off and holidays.

Pay: $145,000.00 - $189,000.00 per year

Benefits:

401(k)
401(k) matching
Health insurance
Paid time off
Relocation assistance

Work Location: In person

Quick Apply

Refine Your Search

manager, regulatory affairs jobs in oceanside ca

Project Manager / Senior Project Manager – Nonclinical Antiviral Development (NIAID Funded Program)

K-8 Teacher / Classroom Manager - Vista USD, CA - $22-40/hr - Open Schedule Afterschool

Community Association Manager

Senior Revenue Cycle Manager

Project Manager

Vendor Manager

Director, Regulatory Affairs

Inside Sales Representative - Wholesaling (No License) - All Inbound Leads

Sr. Manager, Technical Program Management, Experience Team

Manager, Regulatory Affairs

Client Relationship Manager, Employee Group Benefits - Los Angeles or San Diego, CA

Manager, Customer Service Repairs and Returns | Titleist

Manager, Clinic Ops - Family Practice - Jefferson Clinic

ADMINISTRATIVE SERVICES MANAGER

Public Affairs Manager, Southern California

Senior Manager Talent Development & Engagement

Workplace Manager

Program Manager, Healthcare

Sr. Manager, Talent Management

Regulatory Affairs Manager

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