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Biotech Startup Director Clinical Operations Jobs in Riverside, CA

Oasis Health Clinic

HR Manager

San Bernardino, CA · On-site

... startup to full clinical operations. * Establish standardized HR processes, workflows, forms ... Direct experience working for an FQHC or HRSA-funded health center. * Working knowledge of the HRSA ...

Oasis Health Clinic

HR Manager

San Bernardino, CA · On-site

... startup to full clinical operations. * Establish standardized HR processes, workflows, forms ... Direct experience working for an FQHC or HRSA-funded health center. * Working knowledge of the HRSA ...

ACES

Clinic Operations Manager - Ontario

Ontario, CA · On-site

Collaborate with Clinical Directors regularly to meet prescription fulfillment * Coordinate ... Oversee daily clinic operations, including opening and closing procedures; coordinate Manager on ...

ACES

Clinic Operations Manager - Ontario

Ontario, CA · On-site

$70K - $73K/yr

Collaborate with Clinical Directors regularly to meet prescription fulfillment * Coordinate ... Oversee daily clinic operations, including opening and closing procedures; coordinate Manager on ...

BALT Group

Clinical Scientist

Irvine, CA · On-site

... clinical operations, with track record of writing clinical investigation protocols (CIPs) and ... Director of Clinical Evidence. Job Responsibilities Leads implementation of Clinical Evidence ...

BALT Group

Clinical Scientist

Irvine, CA · On-site

... clinical operations, with track record of writing clinical investigation protocols (CIPs) and ... the Director of Clinical Evidence. Job Responsibilities • Leads implementation of Clinical ...

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All JobsBiotech Startup Clinical Operations JobsBiotech Startup Director Clinical Operations JobsBiotech Startup Director Clinical Operations Jobs in Riverside, CA

Biotech Startup Director Clinical Operations information

See Riverside, CA salary details

$62.6K

$152.3K

$294.7K

How much do biotech startup director clinical operations jobs pay per year?

As of Aug 21, 2026, the average yearly pay for biotech startup director clinical operations in Riverside, CA is $152,285.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,400.00 and $181,000.00 per year, depending on experience, location, and employer.

What does a biotech startup director clinical operations do?

A Biotech Startup Director of Clinical Operations oversees the planning, execution, and management of clinical trials at an emerging biotechnology company. Their responsibilities include building and leading the clinical operations team, ensuring regulatory compliance, developing trial protocols, managing budgets and timelines, and collaborating with cross-functional departments like regulatory affairs, medical affairs, and R&D. They play a critical role in advancing new therapies from early-stage trials through to later phases, often in a fast-paced and resource-limited startup environment.

What are the key skills and qualifications needed to thrive as a biotech startup director clinical operations?

To excel as a Biotech Startup Director of Clinical Operations, you need a deep understanding of clinical trial management, regulatory compliance, and drug development, typically supported by an advanced degree in life sciences and significant industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is commonly required. Strong leadership, strategic thinking, and effective communication are essential soft skills for leading teams and collaborating with stakeholders. These competencies ensure that clinical trials are executed efficiently, safely, and in compliance with regulatory standards, which is crucial for the success and growth of a biotech startup.

What are some common challenges faced by a biotech startup director clinical operations, and how can they be addressed?

A Biotech Startup Director of Clinical Operations often faces challenges such as limited resources, rapidly shifting priorities, and the need to establish efficient processes from the ground up. Balancing the demands of regulatory compliance with the agility required in a startup environment can be particularly complex. Success often depends on building a strong, cross-functional team, leveraging external partnerships, and proactively communicating with stakeholders to ensure alignment and timely decision-making. Adapting quickly and fostering a culture of collaboration are essential to overcoming these hurdles.

What is the difference between Biotech Startup Director Clinical Operations vs Clinical Project Manager?

AspectBiotech Startup Director Clinical OperationsClinical Project Manager
ResponsibilitiesOversees all clinical operations, strategic planning, team leadership, and regulatory compliance in a biotech startup setting.Manages individual clinical trials, coordinates project activities, timelines, and budgets under supervision.
Required CredentialsTypically requires advanced degrees (e.g., MS, PhD), clinical research experience, and leadership skills.Requires a bachelor's or master's degree in life sciences or related field, with experience in clinical trial management.
Work EnvironmentFast-paced startup environment with cross-functional teams, high responsibility, and strategic focus.Structured environment within pharmaceutical or biotech companies, focusing on specific trial execution.

The Biotech Startup Director Clinical Operations holds a broader leadership role, overseeing multiple trials and strategic initiatives, while the Clinical Project Manager focuses on managing individual clinical studies. Both roles require clinical research experience, but the director position demands more leadership and strategic planning skills.

What are popular job titles related to Biotech Startup Director Clinical Operations jobs in Riverside, CA?

For Biotech Startup Director Clinical Operations jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Biotech Startup Director Clinical Operations jobs in Riverside, CA look for?

The top searched job categories for Biotech Startup Director Clinical Operations jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Biotech Startup Director Clinical Operations jobs?

Cities near Riverside, CA with the most Biotech Startup Director Clinical Operations job openings:

Biotech Startup Director Clinical Operations jobs near you
Infographic showing various Biotech Startup Director Clinical Operations job openings in Riverside, CA as of June 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Temporary. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $152,285 per year, or $73.2 per hour.

Clinical Study Administrator

Motion Recruitment Partners, LLC

Irvine, CA • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Job Description
Position Title: Clinical Study Administrator
Division: Clinical Operations
Reports To: Study Team Lead
Job Function Summary Overview:
This individual will provide support to the clinical study staff within Clinical Operations
Perform a variety of clinical research operations duties of a routine and technical nature in support of clinical trials.
Supports project managers within the assigned clinical studies.
Key Job Activities: Under direction of Clinical Operations personnel, and in accordance with all applicable Regional, state and local laws/regulations and corporate procedures and guidelines, this position will
  • As directed, provides support to the project teams which may include tracking study data, following-up with clinical sites on essential documents; assist in drafting and distributing study mailings, including study newsletters; assist in drafting of agenda/meeting minutes and scheduling of meetings.
  • Assist in payments/tracking for patient reimbursements.
  • Performs data entry in systems
  • Run reports including training matrix reports, metrics for management reviews
  • Support management of IRB/IEC renewal compliance.
  • Coordinate process for the review of study data, such as MRIs, by third-party vendors.
  • Assist in ordering, shipping, tracking of, study supplies including, but not limited to, investigational devices and site binders. Maintain master device accountability log as requested.
  • Assist with scheduling and organizing investigators and expert panel meetings.
  • Assist with file reviews and Audit preparation
  • Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
  • Work with management group to help achieve department goals.
  • Participate in process improvement activities within the department.
  • May be involved in other tasks to support Clinical Operations and Operating Company as needed.

Other Administrative Tasks
  • Know, understand, incorporate, and comply with all applicable laws and regulations relating to business activities and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
  • May be asked to provide additional support to Clinical Operations staff, as needed.
Job Qualifications
Education
  • Minimum of a Bachelor's Degree is required.

Experience
  • Previous clinical research experience
  • Requires previous administrative support experience or equivalent for at least 1 year.
  • Clinical/medical background

Knowledge
  • Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point).
Additional Requirements
  • Demonstrated competencies in the following areas are required:
    • Tracking
    • Written and verbal communications
    • Attention to details
    • Organizational skills

Apply