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Clinical Trial Report Reviewer Jobs (NOW HIRING)

Syneos Health Inc

Central Report Reviewer

Immediately communicates/escalates serious issues to Clinical Trial Manager/Project Manager. Documents observations noted during reviews and ensures protocol deviations or action items are reported ...

Parexel

Clinical Trial Leader - FSP

Coordinates and supports Trial Medical Writer in providing the Clinical Trial Report (CTR) * Responsible for timely, complete, and compliant archiving of all relevant global documents in the TMF ...

New

C4 Therapeutics Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

... reporting and forecasting to finance (inclusive of site budget review and approval, vendor budget review and approval, and third-party vendor invoice review). * Manage the cross-functional study team ...

New

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... status reports and metrics as requested * Assist with review of monitoring visit reports ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... status reports and metrics as requested * Assist with review of monitoring visit reports ...

CTI

Clinical Trial Manager

Covington, KY · Remote

Provide oversight of visit report review and approval, including site issue escalation and ... Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Coordinates and contributes to the review of relevant study plans and documents including protocols ...

CTI

Clinical Trial Manager

Covington, KY · On-site +1

Provide oversight of visit report review and approval, including site issue escalation and ... Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... This could include a review of monitoring reports and source document review. * Maintain study ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... This could include a review of monitoring reports and source document review. * Maintain study ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

... and reports to senior management on request. • Participate in ongoing study data reviews and ... clinical trial staff on study specific processes. • Other responsibilities as assigned. What ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ... Coordinate Clinical Trial Team meetings and drive action item follow-up. Maintain clinical ...

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Clinical Trial Report Reviewer information

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How much do clinical trial report reviewer jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical trial report reviewer 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 Clinical Trial Report Reviewer vs Clinical Research Associate?

AspectClinical Trial Report ReviewerClinical Research Associate
Required CredentialsBachelor's degree, knowledge of regulatory guidelinesBachelor's degree, often with clinical research certification
Work EnvironmentReviewing clinical trial reports, data analysisMonitoring clinical sites, coordinating trials
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, academic institutions
Common Search & Comparison IntentUnderstanding report review roles, responsibilitiesUnderstanding trial monitoring, site management

The Clinical Trial Report Reviewer primarily focuses on analyzing and reviewing clinical trial reports to ensure accuracy and compliance. In contrast, the Clinical Research Associate is involved in monitoring clinical trial sites and coordinating data collection. Both roles are essential in clinical research, often working together within the same industry environments, but they have distinct responsibilities and skill sets.

What are the key skills and qualifications needed to thrive as a clinical trial report reviewer?

To thrive as a Clinical Trial Report Reviewer, a strong background in clinical research, scientific writing, and regulatory guidelines such as ICH-GCP, often supported by a relevant life sciences degree, is essential. Familiarity with tools like electronic data capture (EDC) systems, document management platforms, and experience with regulatory submission standards are typically required. Attention to detail, critical thinking, and effective communication are key soft skills for ensuring accuracy and clarity in reports. These competencies are crucial for maintaining compliance, ensuring data integrity, and supporting successful regulatory submissions.

What does a clinical trial report reviewer do?

A Clinical Trial Report Reviewer is responsible for evaluating and ensuring the accuracy, completeness, and compliance of clinical trial reports before submission to regulatory authorities. They review documents for clarity, consistency, and adherence to regulatory guidelines like ICH-GCP. This role is crucial for maintaining the integrity of clinical data and supporting the drug approval process. Reviewers often collaborate with clinical researchers, medical writers, and regulatory teams to address any issues or discrepancies found during the review.

What are some common challenges faced by clinical trial report reviewers, and how can they be addressed?

Clinical Trial Report Reviewers often encounter challenges such as tight deadlines, managing complex data sets, and ensuring regulatory compliance. Staying current with evolving guidelines and collaborating closely with cross-functional teams, such as statisticians and medical writers, can help address these challenges. Good organizational skills, attention to detail, and clear communication are essential for meeting quality standards and supporting successful trial submissions.
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Clinical Trial Report Reviewer jobs near you
Infographic showing various Clinical Trial Report Reviewer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% 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.

Central Report Reviewer

Syneos Health Inc

Remote

Other

Posted 6 days ago

Syneos Health rating

8.1

Company rating: 8.1 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical

Job description

Central Report Reviewer

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.• We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Responsible for execution of Central Report Review activities on the study based on the Monitoring strategy defined, with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. May support development of annotated visit reports such as PSV, SIV, IMV, COV & SCAN. Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity. Document requested revisions and approvals in CTMS. Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines. Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations/special Sponsor's requirements and pharmacovigilance issues documented in the report. Immediately communicates/escalates serious issues to Clinical Trial Manager/Project Manager. Documents observations noted during reviews and ensures protocol deviations or action items are reported as necessary in appropriate systems for action by CRA/CM or other functional team members. May assesses CRA/CM report quality, risks, and trends as well as operational performance and summarizes the findings for CTM review and action planning. Participates in clinical monitoring/project staff meetings and attends clinical training sessions according to the project specific requirements. Involves in regular project discussion and email correspondence to maintain the most up-to-date project status knowledge and progression.

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

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