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Research Development Associate Jobs in Temecula, CA

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

... research associates. Key Responsibilities * Oversee daily operations of the in vivo / surgical ... Pharmaron has an excellent track record in delivering R&D solutions to its partners in North ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA

$80K - $100K/yr

... research associates. Key Responsibilities * Oversee daily operations of the in vivo / surgical ... Pharmaron has an excellent track record in delivering R&D solutions to its partners in North ...

IQVIA

Clinical Research Associate

Carlsbad, CA · On-site

$71K - $189K/yr

If applicable, may be accountable for supporting development of project subject recruitment plan on ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...

IQVIA

Clinical Research Associate

Carlsbad, CA

$87K - $182K/yr

If applicable, may be accountable for supporting development of project subject recruitment plan on ... Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements ...

Raya Workforce

Associate Attorney

Temecula, CA · On-site

$150K - $170K/yr

Collaborate with internal teams and contribute to case strategy development * Manage multiple case ... Strong legal research, writing, and analytical skills * Excellent verbal communication and advocacy ...

IQVIA

Clinical Research Associate, Full Service

Carlsbad, CA · On-site

$49K - $175K/yr

If applicable, may be accountable for supporting development of project subject recruitment plan on ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...

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All JobsResearch Development Associate JobsResearch Development Associate Jobs in Temecula, CA

Research Development Associate information

See Temecula, CA salary details

$28.8K

$53.1K

$80.5K

How much do research development associate jobs pay per year?

As of Aug 17, 2026, the average yearly pay for research development associate in Temecula, CA is $53,071.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,200.00 and $59,600.00 per year, depending on experience, location, and employer.

What is a research development associate?

Research Development Associates are professionals who support the development, coordination, and management of research projects, typically within universities, research institutes, or large organizations. Their responsibilities often include identifying funding opportunities, assisting with grant proposal preparation, fostering research collaborations, and ensuring compliance with funding agency guidelines. They serve as a bridge between researchers and administrative offices, helping to maximize research productivity and funding success. Research Development Associates play a key role in advancing institutional research goals and facilitating interdisciplinary initiatives.

What are the key skills and qualifications needed to thrive as a research development associate?

To thrive as a Research Development Associate, you need expertise in grant writing, project management, and research methodologies, often supported by a relevant bachelor's or master's degree. Familiarity with funding databases, proposal submission systems, and data analysis tools is typically required. Strong communication, collaboration, and organizational skills help build relationships with researchers and manage complex projects. These skills ensure effective acquisition of research funding and successful coordination of research initiatives.

How does a research development associate typically collaborate with faculty and research teams to support grant proposals?

As a Research Development Associate, you'll work closely with faculty, principal investigators, and research teams to identify funding opportunities, develop competitive grant proposals, and ensure compliance with institutional and sponsor guidelines. This often involves facilitating brainstorming sessions, coordinating interdisciplinary collaborations, and providing feedback on proposal drafts. You'll also serve as a liaison between researchers and administrative offices, helping to streamline the submission process and enhance the overall quality of proposals.

What is the difference between Research Development Associate vs Research Coordinator?

AspectResearch Development AssociateResearch Coordinator
CredentialsBachelor's or Master's in relevant field, research experienceBachelor's or Master's, often with project management skills
Work EnvironmentResearch labs, academic institutions, industry R&DResearch sites, labs, academic or healthcare settings
Employer & IndustryUniversities, biotech, pharma, research institutesHospitals, universities, research organizations
Primary FocusSupporting research development, grant writing, proposal preparationManaging research projects, data collection, compliance

The Research Development Associate primarily focuses on supporting research initiatives through grant writing and proposal development, while the Research Coordinator manages the day-to-day operations of research projects, including data collection and compliance. Both roles require research experience and are common in academic and industry research settings, but they differ in their core responsibilities and focus areas.

What cities near Temecula, CA are hiring for Research Development Associate jobs?

Cities near Temecula, CA with the most Research Development Associate job openings:

Research Development Associate jobs near you

In Vivo Operations Specialist

Pharmaron

Carlsbad, CA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 3 days ago

Job description

Position: In Vivo Operations Specialist
Salary Range: $80k - $100k (DOE)
Location: Carlsbad, CA (on-site)
About Pharmaron
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, 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 over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ 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 3,000 global customers. To learn more, visit .
Job Overview:
The In Vivo Operations Specialist works closely with the medical device leadership and is responsible for managing day to day laboratory operations and oversight and of the lab activities involving the testing of medical devices and combination products. The In Vivo Operations specialist will also function as a study manager assisting the study directors.
The In vivo operations specialist will be a key member of the Pharmaron Operations Team and function as a liaison between sponsors, internal research scientists, and research associates.
Key Responsibilities
  • Oversee daily operations of the in vivo / surgical research laboratory to ensure studies run safely, efficiently, and on schedule.
  • Coordinate operating room schedules, staffing assignments, equipment readiness, and supply availability.
  • Monitor workflow throughout the day and adjust resources in real time to meet shifting study priorities.
  • Ensure end-of-day closeout activities are completed, including cleaning, restocking, and next-day preparation.
  • Identify operational bottlenecks and implement process improvements to increase efficiency and quality.
  • Partner with Study Directors and scientific leadership to plan and execute preclinical medical device and combination product studies.
  • Maintain the master study calendar, ensuring accurate scheduling, resource allocation, and milestone tracking.
  • Lead internal kickoff meetings to align teams on timelines, protocols, staffing, and study expectations.
  • Support active studies by coordinating logistics, resolving issues quickly, and ensuring timelines are met.
  • Assist with protocol execution, data collection workflows, and report deliverables as needed.
  • Serve as a primary operational point of contact for sponsors before, during, and after study execution.
  • Provide timely updates regarding scheduling, study progress, operational milestones, and deliverables.
  • Respond to sponsor requests professionally, accurately, and with a strong customer-service mindset.
  • Build trusted relationships with clients through responsiveness, reliability, and study excellence.
  • Ensure all activities are performed in accordance with SOPs, USDA regulations, FDA GLP standards, and site policies.
  • Support radiation safety programs including training, documentation, and compliant equipment use.
  • Maintain accurate records for study scheduling, protocols, data, equipment maintenance, and operational metrics.
  • Promote a culture of safety, accountability, and continuous improvement.
  • Assist research teams with animal handling, restraint, dosing, anesthesia support, peri-operative activities, and related procedures as needed.
  • Provide floor support during high-volume or high-priority study days to ensure successful execution.
  • Contribute as a hands-on team member while balancing leadership and operational oversight.

What We're Looking For:
  • Bachelor's degree + 5 years relevant experience, or Master's degree + 1-3 years relevant experience
  • Experience in laboratory, preclinical, CRO, or vivarium environments
  • Experience coordinating operations or projects in fast-paced settings
  • Strong organizational and communication skills
  • Proficiency with Microsoft Office (Excel, Word, Outlook)
  • Anesthesia, analgesia, and peri-operative care experience
  • Protocol/report writing experience
  • Sponsor-facing or client-facing experience

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 21,000 employees and operations in the U.S., the U.K. and China. 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:
  • Insurance including Medical, Dental & Vision with significant 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 an Employee Assistance Program

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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