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Clinical Operations Jobs in San Ramon, CA (NOW HIRING)

Iota Biosciences

Manager, Clinical Operations

Alameda, CA · On-site

$145K - $200K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Role We're seeking a Manager of Clinical Operations to lead the oversight, planning, coordination, and execution of clinical projects for our Class III active implantable device program. This ...

Doist

Director, Clinical Operations

San Francisco, CA · On-site

$215 - $240/hr

Role Overview The Director, Clinical Operations will oversee the strategic and operational execution of clinical trials, leading cross-functional teams and collaborating with internal stakeholders ...

Super Care, LLC

Clinical Operations Lead

Milpitas, CA · On-site

$70K - $123K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Equipment, Telehealth & Operational Support * Serves as an active contributor to clinical purchasing evaluations, including new product reviews, equipment testing, and strategic replacement ...

BigHat

Senior Director, Clinical Operations

San Mateo, CA · On-site

$275 - $295/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Senior Director, Clinical Operations Department: Drug Development Employment Type: Full Time Location: San Mateo, CA Description The role: We are seeking an experienced and motivated Clinical ...

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All JobsClinical Operations JobsClinical Operations Jobs in San Ramon, CA

Clinical Operations information

See San Ramon, CA salary details

$39.1K

$109.6K

$208.4K

How much do clinical operations jobs pay per year?

As of Aug 18, 2026, the average yearly pay for clinical operations in San Ramon, CA is $109,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $126,800.00 per year, depending on experience, location, and employer.

What is clinical operations?

Clinical operations refers to the planning, management, and execution of clinical trials and research studies within the healthcare and pharmaceutical industries. Professionals in clinical operations ensure that studies are conducted efficiently, ethically, and in compliance with regulatory requirements. Their responsibilities may include site management, patient recruitment, data collection, and ensuring protocol adherence. The goal is to facilitate the safe and effective development of new medical treatments and therapies.

How does a clinical operations professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Operations professionals play a central role in coordinating activities among various teams such as regulatory affairs, data management, biostatistics, and clinical research associates. They ensure that timelines are met, protocols are followed, and all departments are aligned with trial objectives. Regular meetings, clear communication, and the ability to anticipate and resolve operational challenges are essential to successful collaboration. This cross-functional teamwork helps maintain trial quality and regulatory compliance throughout the study.

What are the key skills and qualifications needed to thrive in clinical operations, and why are they important?

To thrive in Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and electronic data capture (EDC) platforms is essential. Strong leadership, problem-solving, and communication skills help coordinate teams and ensure project timelines are met. These skills are crucial for guaranteeing efficient, compliant, and successful clinical trial execution in a highly regulated environment.

What is the difference between Clinical Operations vs Clinical Research Associate?

AspectClinical OperationsClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trial managementBachelor's degree, often with certification in clinical research
Work EnvironmentProject management, coordinating multiple trial sitesMonitoring clinical sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies
Common Search & ComparisonFocuses on trial oversight and managementFocuses on site monitoring and data verification

Clinical Operations professionals oversee the planning, coordination, and management of clinical trials, ensuring they run smoothly across multiple sites. Clinical Research Associates primarily monitor clinical trial sites, verify data accuracy, and ensure compliance with protocols. While both roles require knowledge of clinical research, Clinical Operations has a broader scope involving project management, whereas CRAs focus on site-level monitoring.

What are the most commonly searched types of Clinical Operations jobs in San Ramon, CA?

The most popular types of Clinical Operations jobs in San Ramon, CA are:

What job categories do people searching Clinical Operations jobs in San Ramon, CA look for?

The top searched job categories for Clinical Operations jobs in San Ramon, CA are:

What cities near San Ramon, CA are hiring for Clinical Operations jobs?

Cities near San Ramon, CA with the most Clinical Operations job openings:

Clinical Operations jobs near you
Infographic showing various Clinical Operations job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $109,560 per year, or $52.7 per hour.

Manager, Clinical Operations

Iota Biosciences

Alameda, CA • On-site

$145K - $200K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 days ago

Job description

About Us
iota Biosciences, a wholly owned subsidiary of Astellas Pharma US, is advancing a new class of bioelectronic medicines through the development of fully implantable active Class III medical devices. Our proprietary technologies open therapeutic and diagnostic possibilities not previously accessible to clinicians.
Together with Astellas, we are committed to patient-centric design, scientific and engineering excellence, and cross-functional teamwork. These principles guide us in bringing transformative, first-of-its-kind technologies into the clinic and closer to patients.
The Role
We're seeking a Manager of Clinical Operations to lead the oversight, planning, coordination, and execution of clinical projects for our Class III active implantable device program. This role requires direct, hands-on experience running clinical trials for Class III active implantable medical devices.
In this role, you'll manage clinical operations staff and vendors, and help bring a first-of-its-kind bioelectronic therapy to an underserved patient population
What You'll Do
  • Manage a high performing clinical operations team by providing direction, subject matter expertise, training and mentorship.
  • Design, develop, and evaluate clinical execution plans (protocol, CRFs, consent forms, source documents, budgets, timelines, gap analyses).
  • Own end-to-end clinical trial execution: study start-up, site activation, site management, vendor oversight, study reports, and site/study close-out
  • Provide technical direction to clinical research organizations (CROs) and oversee vendor selection/management as needed to execute clinical studies.
  • Work closely with hospitals and investigators participating in clinical studies and maintain close working relationships with KOLs, other investigating physicians and site coordinators
  • Provide input and support for post-clinical activities and market launch of products.
  • Establish / support cross-functional teams to ensure optimal alignment of Clinical, Regulatory, commercial goals, site operations, data monitoring and review, and safety surveillance and reporting expectations.
  • Ensure clinical research programs are conducted in accordance with company standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable regulations.

What we're looking for
  • Bachelor's degree in a scientific field
  • Minimum 8+ years of relevant clinical research experience in the medical device field, or an advanced degree with a minimum of 5 years of relevant experience in the medical device field
  • At least 3 years monitoring experience
  • Experience specifically with Class III medical device clinical studies (required)
  • Proven success building and managing clinical operations teams
  • Comprehensive knowledge of clinical operations including Good Clinical Practices and all applicable US regulations
  • Experience with global clinical studies (e.g., EU or APAC regions)
  • Effective verbal and written communication skills
  • Organized, self-motivated, ability to effectively manage multiple projects and priorities; high attention to detail
  • Must be a strong team player and effectively interface with other departments including translational medicine, regulatory, quality, product development

Preferred Qualifications
  • Clinical research certification (e.g., CCRP, CCRA, etc)
  • Experience with site and sponsor FDA BIMO inspections
  • Superior problem-solving skills.
  • Experience with urology clinical studies
  • Effective interpersonal/communication skills

What makes this role unique:
  • Innovation - first of its kind device that will require a unique clinical study design.
  • Build & Lead - you'll bring clinical operations expertise to the department and have the opportunity to influence department strategy and implementation
  • Impact - clinical studies are a critical part of product development. Your work here will directly influence time to market and providing a new therapy to an underserved patient population.

iota offers a very competitive benefits package that includes the following:
Health & Wellness
  • Comprehensive health coverage for you and your family, covered at 100%
  • Access to quality dental and vision coverage
  • Onsite Gym in Alameda

Work-Life Balance
  • Generous vacation pay
  • Paid parental leave
  • Options for flexible work schedules

Competitive Compensation
  • Annual Bonus Plan
  • Long Term Incentive Plan (LTIP)
  • 401(k) plan with employer match

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