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Clinical Trial Report Reviewer Jobs (NOW HIRING)

Parexel

Clinical Trial Leader

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 ...

Parexel

Global 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 ...

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 ...

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers and ...

New

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers and ...

New

ICON

Clinical Trial Assistant

San Francisco, CA · On-site

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers and ...

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 ...

ICON

Clinical Trial Assistant

San Francisco, CA · On-site

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers 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 · 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 ...

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 ...

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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 15, 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, 72% 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 Leader

Parexel

Remote

Full-time

Posted 4 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 73 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
All US locations
Job Description Summary
The Clinical Trial Leader -CTLs are accountable for the set-up, execution and delivery of their assigned trial(s) and contribute to delivery of client's pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites. The CTL provides leadership and direction to the trial team (core and extended team members) and is accountable for the overall success and delivery of their assigned clinical trial according to defined milestones and key performance indicators. They are responsible for steering and directing clinical trial activities, including patient and site engagement activities, direct communication, and interaction with multiple internal and external stakeholders (e.g. investigative sites) and team members on a global, multi-country or regional basis. The CTL is responsible for managing the planning, implementation, and tracking of the clinical trial process as well as risk mitigation. The CTL serves as a proactive member of the clinical delivery team, liaising closely with the Clinical Trial Managers ("CTM") on all study-related issues. As leader of the Trial Team, the CTL communicates trial status to stakeholders, escalating issues as appropriate.
Key Accountabilities:
Trial Preparation
  • Accountable for the accurate planning and operational feasibility of trial timelines; and oversight of trial preparation to ensure trial team members are aligned and on track. Supports development of trial level documents owned by other functions (e.g. Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring)
  • Verifies and provides input into the country allocation and oversees trial feasibility
  • Accountable for development and implementation of trial level engagement plans, recruitment planning and risk mitigation
  • Leads development of core trial and patient facing documents
  • Integrates patient/site level feedback during document development and ensures trials are designed with a focus on patient value
  • Ensures activities are frontloaded where possible at the trial level and cascaded to country level to facilitate efficiencies as well as to ensure and leverage speed
  • Oversees outsourcing of vendor services in conjunction with other functions; supports identification of vendors, vendor selection and development of vendor scope of work
  • Works with functional partners to ensure that all required trial processes are in place to meet trial delivery milestones (e.g. clinical quality monitoring, safety monitoring and reporting, investigational medicinal product, trial budget, site monitoring)
  • Aligns and supports team members in timely responses to questions from Regulatory Authority/Ethics Committee and other external stakeholders
  • Provides/supports provision of appropriate study- specific and standardized non-trial specific trial team training, internal and external partners

Trial Conduct
  • Maintains oversight during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; compliance with SOPs and continuous risk monitoring/mitigation
  • In collaboration with other functions, ensures budget oversight, including support of regular clinical quality monitoring, Safety Management Committee (SMC)/Data Management Committee (DMC) management and safety reporting
  • Prepare and implement amendments of core documents including training material updates/retraining as needed
  • Support authority/ethics responses to requests as applicable
  • Maintains oversight of outsourcing of vendor services (including central lab) in conjunction with other functions
  • Monitor progress of patient recruitment and accrual of endpoints and proactively update and action contingencies throughout trial conduct.
  • For early clinical trials, co-ordinates and harmonizes Innovation Unit tasks in a trial (e.g. biomarker sampling, genomics, sub-studies)

Trial Closeout and Reporting
  • In collaboration with other functions, ensures timely cleaning and delivery of clinical trial data
  • 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, including all require documents from vendors.
  • Support results/documents disclosure of global registries
  • May support publication of trial data

Contributions to Trial Strategy
  • Supports preparation and execution of clinical trials, including: (i) planning of trial milestones; (ii) contributing operational and scientific expertise; and iii) considering and planning for regulatory interactions
  • Supports Clinical Development and Operations Lead (CDOL) to ensure issues are raised to Client's Evidence team for timely action or mitigation
  • Responsible for the Trial Feasibility activities that define key aspects of a Clinical Trial Protocol (CTP)

Leadership competencies
  • Creates an environment that inspires, motivates, and empowers colleagues and promotes client's Clinical Development and Operations (CD&O) identity, contributing to acceleration of clinical development timelines and value creation for patients
  • Fosters a learning culture in client's CD&O regions by encouraging continuous learning, sharing best practices, and learning from failures
  • Embraces innovative technologies, as well as creates and maintains a culture that drives empowerment, smart risk taking and client's CD&O identity

Compliance with Parexel standards
  • Comply with required training curriculum
  • Complete timesheets accurately as required
  • Submit expense reports as required
  • Update CV as required
  • Maintain a working knowledge of and comply with Parexel processes, ICHGCPs and other applicable requirements

Skills:
  • Strong clinical trial project management experience. In-depth understanding of project management with emphasis on team work to promote high-performance teams
  • Experience in Therapeutic Areas relevant in client pipeline is desirable
  • Understanding of major regulations (US FDA, EMA and PMDA)
  • Familiarity with guidelines and standard of care is desirable
  • Cross geographical experience. Working in multi-cultural environment; strong understanding of corporate culture and cross-cultural dynamics
  • Strengths in mentoring/coaching
  • Demonstrated competencies in Agility, Accountability, and Intrapreneurship: fast decision-making, flexibility, ownership, outcome-based thinking, results orientation, and smart risk-taking

Knowledge and Experience:
  • Strong Communication Skills: Articulates and aligns business strategy/plan on an ongoing basis, ensuring alignment between words and action. Demonstrates active listening skills and cultural awareness.
  • Scientific and Operational Expertise: Demonstrates scientific and therapeutic knowledge and operational expertise across all aspects of clinical trial planning and execution. Dimensions of trial complexity include protocol, patients, sites, countries, vendors. Extensive experience in clinical trial project management in an international context.
  • Leadership and Influence: Demonstrates skills and capabilities in addressing complex situations, confidently setting direction for teams. Demonstrates leadership behaviors of supporting, connecting, and empowering teams, providing future direction, demonstrating visionary and innovative thinking and inspiring teams to achieve a common goal. Executes activities with a clear aim to deliver value to patients.
  • Strategic Mindset: Strategic and visionary thinker who is future focused, creative, courageous, and able to navigate through ambiguity. Integrates study strategy with overall TA portfolio. Embraces cross functional initiatives, applying innovative learnings. Is results-oriented with a global mindset using analytical thinking to provide risk-balanced solutions.
  • Coordination and Oversight: Collaborative leader who demonstrates skills and capabilities in setting priorities, managing pace of activities, and efficient usage of resources.
  • Project Management: Plans effectively, setting priorities, and defining actions. Makes effective use of resources, and proactively strives for transparency and clarity to accomplish the business deliverables. Translates complex situations to actionable parts. Anticipates and resolves challenges and translates learnings to new projects. Takes smart risks.

Education:
  • Requires a university degree (e.g. bachelor's or advanced degree). Major focus: Biomedical Life Sciences.

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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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