ZipRecruiter

Log In

2

Remote Clinical Trial Operations Jobs (NOW HIRING)

Catalyst Pharmaceuticals, Inc.

Clinical Trial Manager

$130K - $147K/yr

The Clinical Trial Manager (CTM) provides end-to-end leadership and operational oversight for assigned clinical programs, driving execution of Clinical Trial Team activities across the study ...

New

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... This position is for remote work and may require domestic or international travel up to 25% (as ...

Bruno

Clinical Payments Specialist

Raleigh, NC · Remote

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations Specialist to support global clinical trial operations by managing investigator budgets, site setup, and ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

... smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Collaborate across functions and with vendor partners to resolve operational barriers, ensuring ...

next page

Showing results 1-20

All JobsClinical Trial Operations JobsRemote Clinical Trial Operations Jobs

Remote Clinical Trial Operations information

See salary details

$17

$39

$70

How much do remote clinical trial operations jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for remote clinical trial operations in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trial Operations vs Remote Clinical Trial Coordinators?

AspectRemote Clinical Trial OperationsRemote Clinical Trial Coordinators
ResponsibilitiesOversees trial processes, manages site logistics, ensures complianceSupports trial activities, manages participant schedules, assists with data collection
Required CredentialsTypically requires a degree in life sciences, clinical research certificationOften requires a degree or certification in clinical research or related field
Work EnvironmentRemote, with collaboration across sites and teamsPrimarily remote, working closely with trial sites and participants
Industry UsageCommon in pharmaceutical and biotech companiesCommon in research organizations and CROs

Remote Clinical Trial Operations professionals focus on managing and overseeing the entire trial process, ensuring compliance and efficiency. In contrast, Remote Clinical Trial Coordinators handle day-to-day participant management and data collection. Both roles require clinical research knowledge and often work remotely, but their scope and responsibilities differ significantly.

More about Remote Clinical Trial Operations jobs
What cities are hiring for Remote Clinical Trial Operations jobs? Cities with the most Remote Clinical Trial Operations job openings:
What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Remote Clinical Trial Operations jobs? States with the most job openings for Remote Clinical Trial Operations jobs include:
What job categories do people searching Remote Clinical Trial Operations jobs look for? The top searched job categories for Remote Clinical Trial Operations jobs are:
Remote Clinical Trial Operations jobs near you
Infographic showing various Remote Clinical Trial Operations job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Clinical Trial Manager

Clinical Trial Manager

Catalyst Pharmaceuticals, Inc.

Remote

$130K - $147K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted yesterday

Job description

The Clinical Trial Manager (CTM) provides end-to-end leadership and operational oversight for assigned clinical programs, driving execution of Clinical Trial Team activities across the study lifecycle. In close partnership with the Sr. Director, Clinical Development and Clinical Operations Leadership, the CTM is accountable for the integrated delivery of clinical trials ensuring alignment with corporate strategy and full compliance with regulatory, GCP, and quality standards.
The CTM serves as the central orchestrator of cross-functional teams, proactively managing timelines, budgets, resources, and risks to deliver studies on time, within scope, and on budget. This role emphasizes data-driven decision-making, vendor and stakeholder management, and continuous process optimization to enable high-quality, inspection-ready clinical execution.
Requirements
Responsibilities (include but not limited to) :
  • Program & Study Execution Leadership: Leads development and execution of integrated clinical program and study-level plans in partnership with cross-functional stakeholders, ensuring alignment with overall development strategy, regulatory requirements, and corporate objectives
  • CRO & Vendor Oversight: Provides strategic oversight and performance management of CROs, vendors, and external partners, including governance, KPI tracking, and issue escalation to ensure high-quality, cost-effective delivery
  • Cross-Functional Integration & Planning: Collaborates with Clinical Operations, Clinical Development, Regulatory, Biostatistics, Data Management, and other functional areas to develop and maintain realistic timelines, budgets, and resource plans; identifies and proactively manages critical path activities and dependencies
  • Risk-Based Study Management: Implements and drives risk-based trial management approaches, including proactive risk identification, mitigation planning, and continuous monitoring of key study risks and operational signals
  • Performance & Delivery Management: Monitors study progress against milestones, deliverables, and KPIs using data-driven insights; proactively identifies variances and leads corrective and preventive actions to ensure on-time, within-scope, and on-budget delivery
  • Stakeholder Communication & Governance: Ensures transparent, timely, and effective communication of program status, risks, decisions, and milestones to internal and external stakeholders through structured governance, reporting, and escalation pathways
  • Cross-Functional Leadership & Influence: Demonstrates the ability to appropriately challenge, influence, and motivate cross-functional team members and partners to drive accountability, decision-making, and high-performance execution across multiple concurrent studies
  • Quality & Inspection Readiness: Ensures clinical studies are continuously inspection-ready, with adherence to GCP, SOPs, and regulatory requirements; leads preparation for audits/inspections and ensures timely resolution of findings through effective CAPA management
  • Operational Excellence & Continuous Improvement: Identifies opportunities to enhance processes, tools, and ways of working; contributes to the implementation of innovative solutions (i.e. digital tools, decentralized trial elements, AI analytics) to improve study execution
  • Additional Responsibilities: Performs other duties as assigned, consistent with the evolving needs of the clinical development organization

Education/Experience/Skills :
  • Bachelor's degree in science/health-related field; Master's degree is preferred.
  • 5 to 7 years of clinical research experience with at least 5 years of clinical trial management experience.
  • A thorough and working understanding of FDA and GCP/ICH guidelines.
  • Excellent written and oral communication skills with the ability to manage multiple priorities.
  • Ability to travel 25% to clinical trial sites and/or CROs

Catalyst is committed to providing competitive wages and comprehensive benefits including health, dental, and vision insurance, generous paid time off, a retirement savings plan with Company Match, and more. Further details about our benefits package can be found here: https://www.linkedin.com/company/catalystforrare/life/life-at-catalyst/?viewAsMember=true
The base salary for this position will range from $130,000 to $147,000. Candidate experience, professional licensing, and geographic location will be taken into consideration.
Employment is contingent upon successful completion of all required screening and verification processes, including for authority to work in the United States.
EEO Statement
Catalyst Pharmaceuticals is an Equal Opportunity Employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status.
Recruitment & Staffing Agencies: Catalyst Pharmaceuticals does not accept unsolicited agency resumes. Agency resumes will only be accepted if the agency is formally engaged by Catalyst Human Resources.

Apply