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Clinical Research Executive Jobs (NOW HIRING)

Phsorg

The Director of Clinical Research is the senior executive responsible for the strategic, operational, and regulatory leadership of the Presbyterian Healthcare Services clinical research enterprise.

NYULMC

Program Lead, Clinical Research

New York, NY · On-site

Partners with executive leadership to identify operational risks, financial gaps, and process improvement opportunities related to study activation and clinical research center financial ...

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How much do clinical research executive jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical research executive in the United States is $27.65, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $29.81 per hour, depending on experience, location, and employer.

What does a clinical research executive do?

A Clinical Research Executive is responsible for overseeing and coordinating clinical trials and research activities within healthcare or pharmaceutical organizations. They ensure studies are conducted according to regulatory guidelines and protocols, manage project timelines, and liaise with research teams, ethics committees, and sponsors. Their role often includes budgeting, reporting, and ensuring the integrity and safety of clinical data. Clinical Research Executives play a key part in bringing new medical treatments and therapies to market by ensuring high standards of research quality and compliance.

What are the key skills and qualifications needed to thrive as a clinical research executive?

To thrive as a Clinical Research Executive, you need a solid background in life sciences or pharmacy, experience in clinical trial management, and a thorough understanding of regulatory guidelines such as GCP. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP are typically required. Strong organizational skills, attention to detail, and effective communication are vital soft skills that set top performers apart. These competencies ensure clinical trials are conducted efficiently, ethically, and in compliance with industry standards, leading to reliable research outcomes.

How does a clinical research executive typically collaborate with cross-functional teams during a clinical trial?

A Clinical Research Executive works closely with various cross-functional teams, including clinical operations, regulatory affairs, data management, and medical writing, to ensure the smooth execution of clinical trials. This role often acts as a central point of communication, coordinating timelines, sharing updates, and resolving issues that may arise during the study. Regular meetings, joint planning sessions, and collaborative problem-solving are key aspects of the role, helping to ensure that all departments are aligned with trial objectives, regulatory requirements, and patient safety protocols.

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

AspectClinical Research ExecutiveClinical Research Associate
CredentialsBachelor's or Master's in Life Sciences, certifications like CCRP or RACBachelor's in Life Sciences, often similar certifications
Work EnvironmentOffice-based, overseeing research projects, liaising with teamsSite visits, monitoring clinical trials, data collection
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch sites, hospitals, CROs

While both roles are involved in clinical research, the Clinical Research Executive primarily manages and oversees research projects from an administrative and strategic perspective, often working in an office environment. In contrast, the Clinical Research Associate is more hands-on, monitoring clinical trials at research sites. Both roles require similar credentials and are integral to the clinical research process, but they differ in daily responsibilities and work settings.

What is a clinical research executive?

A clinical research executive is a professional responsible for overseeing and managing clinical trials to ensure they are conducted according to regulatory standards and study protocols. They coordinate between research teams, sponsors, and regulatory bodies, often requiring knowledge of Good Clinical Practice (GCP) and relevant software tools. This role typically involves strategic planning, compliance monitoring, and reporting to support the development of new medical treatments.
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Clinical Research Executive jobs near you
Infographic showing various Clinical Research Executive job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $57,519 per year, or $27.7 per hour.

Clinical Research Coordinator

Washington, DC • On-site

Dynamics ATS Organic
See more jobs at Dynamics ATS Organicexternal

$50K - $60K/yr

Full-time

Posted 3 days ago

New

Job description

Clinical Research Coordinator

Trusted Medical is seeking an experienced Clinical Research Coordinator (CRC) to support our growing national clinical trials program. This position plays a key role in coordinating clinical research activities, maintaining regulatory compliance, supporting study participants, and ensuring trials remain on schedule from initiation through closeout.

The ideal candidate is highly organized, detail-oriented, knowledgeable in clinical research regulations, and comfortable managing multiple studies and stakeholders in a fast-paced environment.

Employment Type: Full-Time, W-2

Location: Washington, DC / Regional Clinic-Based Salary Range: $50,000–$60,000 annually, with potential performance-based incentives

Travel: Occasional travel may be required for national study meetings or site activities Reports To: Nurse Executive

Key Responsibilities

*             Coordinate day-to-day operations for assigned clinical trials from study initiation through closeout.

*             Recruit, screen, consent, enroll, and support study participants in accordance with approved protocols.

*             Schedule and coordinate study visits, procedures, assessments, and follow-up appointments.

*             Maintain accurate source documentation, case report forms, regulatory binders, study logs, and essential study records.

*             Prepare and submit regulatory documentation to IRBs, sponsors, and applicable regulatory agencies.

*             Ensure compliance with FDA regulations, ICH-GCP, OHRP requirements, HIPAA, study protocols, and internal SOPs.

*             Monitor protocol adherence and proactively identify and resolve study deviations.

*             Track and report adverse events (AEs), serious adverse events (SAEs), enrollment goals, retention, and study milestones.

*             Manage investigational product inventory, storage, dispensing, accountability, and return, when applicable.

*             Enter and verify clinical data within electronic data capture systems and resolve data queries promptly.

*             Coordinate specimen collection, processing, and shipment to central laboratories or biorepositories.

*             Serve as a primary point of contact for investigators, sponsors, CROs, study monitors, auditors, vendors, and internal clinical teams.

*             Support monitoring visits, audits, quality assurance reviews, site initiation activities, and study closeout.

*             Assist with study budgets, invoicing, payment tracking, feasibility assessments, recruitment materials, and IRB communications.

*             Participate in sponsor, CRO, and consortium training meetings as required.

Required Qualifications

*             Bachelor’s degree in life sciences, healthcare, clinical research, or a related field.

*             5+ years of clinical research experience, preferably supporting multiple or national clinical studies.

*             Strong knowledge of FDA regulations, ICH-GCP guidelines, IRB processes, informed consent requirements, and clinical research protocols.

*             Experience with regulatory submissions and electronic data capture systems.

*             Proficiency with clinical research platforms such as REDCap, Medidata Rave, or similar systems.

*             Strong proficiency with Microsoft Word, Excel, PowerPoint, and related productivity tools.

*             Excellent written and verbal communication, organizational, and problem-solving skills.

*             Ability to work independently while collaborating effectively across clinical and operational teams.

Preferred Qualifications

*             ACRP-CRC or SOCRA-CCRC certification.

*             Experience supporting NIH, CMS, FDA-sponsored, pharmaceutical, or federally funded research studies.

*             Experience with multi-site clinical trials.

Additional Requirements

Candidates must be U.S. citizens and eligible to obtain a Public Trust clearance. Trusted Medical participates in E-Verify and maintains a drug-free workplace.

Join a growing clinical research organization where your expertise will directly support high-quality research, improved study access, and meaningful outcomes for Veterans, active-duty service members, and communities nationwide.