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Contract Clinical Operations Jobs (NOW HIRING)

Tr1X

Director, Clinical Operations

San Diego, CA · On-site

The Director is accountable for leading cross-functional clinical study teams; directing contract ... This role serves as a key operational leader within the organization and is responsible for ...

Tr1X

Director, Clinical Operations

San Diego, CA · On-site

The Director is accountable for leading cross-functional clinical study teams; directing contract ... This role serves as a key operational leader within the organization and is responsible for ...

Tr1X

Director, Clinical Operations

San Diego, CA

The Director is accountable for leading cross-functional clinical study teams; directing contract ... This role serves as a key operational leader within the organization and is responsible for ...

Wake Research

Clinical Operations Lead

Raleigh, NC · Remote

The Clinical Operations Lead serves as a central point of coordination between sites, sponsors ... Contract Research Organization (CRO) * Experience as a Clinical Research Coordinator and/or ...

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$35K

$98K

$186.5K

How much do contract clinical operations jobs pay per year?

As of Jun 6, 2026, the average yearly pay for contract clinical operations in the United States is $98,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $113,500.00 per year, depending on experience, location, and employer.

What are Contract Clinical Operations?

Contract Clinical Operations refer to the management and oversight of clinical trials and research activities that are conducted on a contractual basis, often by external vendors or contract research organizations (CROs). Professionals in this role ensure that clinical studies comply with regulatory requirements, timelines, and budgets while maintaining data integrity and participant safety. They coordinate tasks such as site selection, trial initiation, monitoring, and reporting, often acting as a liaison between sponsors and service providers. This role is essential for pharmaceutical, biotechnology, and medical device companies that outsource clinical research to meet project demands efficiently.

What are the key skills and qualifications needed to thrive in Contract Clinical Operations, and why are they important?

To thrive in Contract Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and contract negotiation, often backed by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of ICH-GCP guidelines are typically required. Strong organizational skills, attention to detail, and effective communication help professionals excel in managing multiple stakeholders and timelines. These capabilities ensure clinical studies are executed efficiently, ethically, and in accordance with regulatory standards.

What are some common challenges faced in a Contract Clinical Operations role, and how can they be managed effectively?

Professionals in Contract Clinical Operations often encounter challenges such as coordinating multiple clinical trials across various sites, managing tight timelines, and ensuring strict regulatory compliance. Balancing the needs of sponsors, vendors, and cross-functional teams requires strong communication and organizational skills. Staying proactive, leveraging digital project management tools, and maintaining clear documentation can help address these challenges effectively. Collaborating closely with clinical research associates, data managers, and regulatory specialists is key to ensuring smooth trial execution and problem resolution.
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Contract Clinical Operations jobs near you
Clinical Operations Specialist

Clinical Operations Specialist

A-Line Staffing Solutions

Irvine, CA • On-site

$30 - $35/hr

Full-time

Retirement

This job post has expired today. Applications are no longer accepted.

Job description

A-Line Staffing is now hiring a Full Time, On-Site, Clinical Operations Specialist in Irvine, CA! Job Summary: We are seeking a Specialist I, Clinical Operations to support clinical trial activities and device lifecycle management. This role focuses on process improvement, inventory coordination, and ensuring compliance across clinical operations.

The ideal candidate will bring hands-on clinical experience along with strong organizational and analytical skills. Clinical Operations Specialist Compensation The pay for this position is $30-35 (will state the rate with offer) Benefits are available to full-time employees after 90 days of employment A 401(k) with a company match is available for full-time employees with 1 year of service on our eligibility dates Clinical Operations Specialist Highlights This position is a contract assignment with potential to hire on permanently based upon attendance, performance, and business needs The required availability for this position is M-F, 8am-5pm Clinical Operations Specialist Responsibilities · Identify, develop, and implement moderately complex process improvements to optimize clinical trial workflows and timelines · Develop and execute device-related processes associated with clinical trials · Ensure compliance with regulatory requirements and manage device lifecycle activities · Collaborate cross-functionally with Clinical Study Teams, Manufacturing, Supply Chain, Finance, Quality, and Compliance · Verify inventory and coordinate device shipments to clinical sites within required timelines · Confirm product receipt with clinical sites and maintain accurate documentation · Monitor device inventory in partnership with Supply Chain and Clinical Specialists · Develop timeline assessments to support study milestones and system transitions · Maintain proper documentation and archival in record retention systems (e.g., Iron Mountain, ClinicalTrials.gov) · Track, manage, and coordinate clinical study invoice processing and payments · Generate reports on outstanding invoices for clinical team review · Review clinical study files for accuracy and completeness; maintain records in tracking systems · Maintain current certifications (CPR, First Aid, BLS) for clinical research support · Provide support to clinical research lab operations as needed · Perform additional duties as assigned · Required Technical Skills 1–2 years of patient-facing experience in clinical research, healthcare, or a related medical setting Current CPR and First Aid certification from an accredited provider Preferred Qualifications 2+ years of experience in a clinical role (e.g., EMT, Medical Assistant) Associate's or Bachelor's degree in a related field If you think this Clinical Operations Specialist position is a good fit for you, please reach out to me—feel free to call, e-mail, or apply to this posting!

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About A-Line Staffing Solutions

Sourced by ZipRecruiter

A-Line Staffing Solutions is an established full-service recruiting and staffing provider that operates in the industry of human resources and recruitment. Based in Utica, Michigan, A-Line Staffing Solutions has been committed to its mission of providing innovative and effective workforce solutions since its foundation. The company specializes in providing high-quality staffing solutions for a range of disciplines, including Information Technology, Professional, Administrative, Healthcare, and more. A-Line prides itself on its ability to offer comprehensive and tailored staffing solutions in line with the varying needs of different businesses, which has played a crucial role in the company's growth and success.

Industry

Recruiting and staffing services

Company size

201 - 500 Employees

Headquarters location

Utica, MI, US

Year founded

2004

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