2

Locum Remote Clinical Operations Jobs in California

Clinical Program Manager

Eureka, CA ยท Remote

$33 - $40/hr

The Clinical Manager plays a key role in supporting the day-to-day operations of the clinical ... Work Location: Remote Benefits: * 401(k) with Employer Matching * Paid Vacation, Sick Days ...

Clinical Research Associate

Irvine, CA ยท Remote

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...

Sr Clinical Trials Manager

Foster City, CA ยท On-site +1

$157K - $203K/yr

Clinical Operations leads the global execution of Phase I-IV clinical trials across therapeutic ... Will not consider fully remote candidates. Responsibilities: * Lead all aspects of assigned ...

Sr Clinical Trials Manager

Foster City, CA ยท On-site +1

$157K - $203K/yr

Clinical Operations leads the global execution of Phase I-IV clinical trials across therapeutic ... Will not consider fully remote candidates. Responsibilities: * Lead all aspects of assigned ...

Showing results 41-60

Locum Remote Clinical Operations information

What is the difference between Locum Remote Clinical Operations vs Remote Clinical Project Coordinator?

AspectLocum Remote Clinical OperationsRemote Clinical Project Coordinator
CredentialsClinical background, certifications in healthcare or clinical researchProject management certifications, healthcare or research experience
Work EnvironmentRemote, flexible, often contract-basedRemote, team collaboration, project-focused
Employer & Industry UsageHospitals, research organizations, healthcare companiesPharmaceutical companies, CROs, research institutions
Search & Comparison IntentTemporary clinical operations roles, healthcare project supportManaging clinical projects remotely, coordinating research activities

While both roles involve remote work in the clinical research industry, Locum Remote Clinical Operations typically refers to temporary, contract-based positions focused on overseeing clinical processes, whereas Remote Clinical Project Coordinators manage specific research projects remotely, often with a focus on coordination and communication. Both require healthcare or research experience but differ in scope and responsibilities.

What are the most commonly searched types of Remote Clinical Operations jobs in California?

The most popular types of Remote Clinical Operations jobs in California are:

What are popular job titles related to Locum Remote Clinical Operations jobs in California?

For Locum Remote Clinical Operations jobs in California, the most frequently searched job titles are:

What job categories do people searching Locum Remote Clinical Operations jobs in California look for?

The top searched job categories for Locum Remote Clinical Operations jobs in California are:

What cities in California are hiring for Locum Remote Clinical Operations jobs?

Cities in California with the most Locum Remote Clinical Operations job openings:

Infographic showing various Locum Remote Clinical Operations job openings in California as of August 2026, with employment types broken down into 83% Full Time, 14% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

Sr Director, Clinical Sciences

Welcome to the Tarsanet Internal Career Center!

Irvine, CA โ€ข On-site, Remote

$85K - $117K/yr

Full-time

Medical, Dental, Vision, PTO

Posted 14 days ago


Job description

About the Role

The Sr Director, Clinical Sciences will lead Clinical Science (Eyecare) function, accountable for the scientific integrity, quality, and strategic impact of all eyecare clinical studies from early development through late-stage registration and lifecycle management. This role partners closely with Clinical Operations, Regulatory, Biostats, Medical Affairs, and Commercial to translate target product profiles into robust clinical development plans and highquality trial designs.

Let's talk about some of the key responsibilities of the role:

  • Provide scientific leadership to crossfunctional study and program teams, ensuring timely study startup, enrollment, database lock, analysis, and readouts.
  • Lead the design of clinical development plans and individual study protocols (objectives, endpoints, inclusion/exclusion, assessments, statistical assumptions)
  • Maintains direct ownership of clinical deliverables, actively contributing to protocol development, document authoring, data review, study-level problem solving and execution decisions to ensure scientific rigor and operational excellence.
  • Shape clinical plans including timelines, budgets and oversight of clinical teams.
  • Build and maintain strong relationships with investigators, KOLs, and external partners; contribute to publication strategy and scientific communications
  • Drive innovation in clinical endpoints, biomarkers, and digital tools, and champion continuous improvement in clinical science processes, templates, and data review frameworks
  • Author and critically review key clinical and regulatory documents, including protocols, SAPs, CSRs, IBs and clinical value dossiers, ensuring scientific rigor, regulatory alignment and quality execution.
  • Conduct research to develop foundational education material to inform the early development program strategies.
  • Interpret clinical data and support data-driven decisions.
  • Serve as program lead on early development Core teams, investigator meetings and scientific advisory boards.
  • Engage with internal and external stakeholders, including KOLs and regulators.
  • Exhibits and fosters key leadership competencies, including an innovative mindset, strong business acumen, an outcome-driven orientation, and a commitment to growing and expanding the capabilities and capacity of the team.
  • Collaborate with Clinical Operations, Regulatory Affairs, Translational Sciences, Biostatistics, Medical Affairs and others to ensure robust trial design, scientific and operational alignment and execution .

Factors for Success:

  • Advanced degree in sciences (e.g. PharmD, MD, PhD) with deep experience in early clinical development
  • Experience in ophthalmology is preferred; dermatology or infectious diseases a plus.
  • Minimum of 10 years of biotech/pharmaceutical clinical development experience, with a minimum of 8 years leadership in clinical trial management experience required
  • Established leadership track record with evidence of excellent performance-based people management experience, problem solving, collaboration, cross functional leadership and effective communication skills.
  • Expertise with SOPs, GCPs and regulatory and compliance guidelines for clinical trials.
  • Must be willing to be "hands on" and delve into details

Leadership Competencies - This role requires mastery of the Tarsus Leadership Competencies for Leading Teams, including:

  • Empowering Others - Fosters empowerment by aligning authority with accountability, developing leaders' decision-making capability, and creating systems that support performance and growth.
  • Emotional Intelligence - Foster trust and psychological safety, navigating complex interpersonal dynamics with compassion and accountability, and adapting leadership style to support others while maintaining composure under pressure.
  • Grows Capacity - Builds organizational capacity by developing talent systems, coaching cultures, and strategic partnerships that grow leadership strength and prepare the next generation of leaders.
  • Business Acumen - Demonstrates strong business acumen by anticipating market dynamics and using financial and strategic insight to guide investments, manage risk, and align priorities with long-term organizational value.
  • Innovative Mindset and Action - Demonstrates an innovative mindset by championing new ideas, investing in enabling systems and partnerships, and translating innovation into sustainable growth and organizational resilience.

ย Few Other Details Worth Mentioning:

  • The position will be based in our beautiful Irvine office, complete with onsite gym, pool, snacks, drinks, and occasional catered meals. We provide a hybrid work environment. Remote work is an option.
  • We are passionate about our culture! Our Tarsans live our values of commitment to patients, empowerment to champion innovation, and teamwork to amplify impact!
  • This position reports directly to our SVP, Development
  • Some travel may be required - up to 30%

At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $255,000 - $357,000 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.

#LI-Remote