Clinical Data Manager/Clinical Data Reviewer

Charles River Laboratories; United States; Remote; USD 80,000 - 110,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Pension plan

Paid paternity leave

Job summary

A leading global healthcare company is seeking an experienced Clinical Data Manager/Clinical Data Reviewer for a full-time, remote role. You will support clinical data management processes, ensure data integrity, and collaborate with clients on complex studies. The ideal candidate has a scientific background and experience in a pharmaceutical environment, proficient in CDISC standards, and excels in communication and relationship-building. This position offers an impactful role in advancing global health.

Qualifications

• Bachelor’s degree in a scientific discipline preferred.
• Strong background in a research or pharmaceutical environment.
• Hands-on clinical data management and review experience required.

Responsibilities

• Prepare and review Data Transfer Agreements for all assay data types.
• Review clinical trial data for accuracy, completeness, and protocol adherence.
• Develop and maintain templates, tools, and SOPs.

Skills

Clinical data management

Client relationship building

Data quality control

Knowledge of CDISC standards

Strong communication skills

Organizational skills

Education

Bachelor’s degree in a scientific discipline

Tools

Microsoft Office

Job description

Clinical Data Manager/Clinical Data Reviewer

Join to apply for the Clinical Data Manager/Clinical Data Reviewer role at Charles River Laboratories

For 75+ years, Charles River has advanced the discovery, development, and safe manufacture of new drug therapies. Join a global team where your expertise directly supports healthier lives worldwide.

We are seeking an experienced Clinical Data Manager/Clinical Data Reviewer to join our Safety Assessment business on a full-time, permanent, remote basis (UK or EU). In this role, you’ll support end-to-end clinical data management processes, ensure data integrity, and collaborate closely with clients across multiple complex studies.

Clinical Data Management & Transfer

• Prepare and review Data Transfer Agreements for all assay data types.
• Build strong client relationships through regular meetings and data presentations.
• Create and QC SDTM and non-SDTM datasets.
• Ensure all datasets meet regulatory standards and are delivered securely.
• Use approved data exchange platforms for compliant data transfers.

Data Review & Quality

• Review clinical trial data for accuracy, completeness, and protocol adherence.
• Validate data coding, interpretation, and consistency.
• Conduct robust QC checks across all study documentation and regulatory requirements.
• Partner with internal teams and external clients throughout the data lifecycle.
• Mentor and support peers; serve as team lead when applicable (Manager level).
• Host and participate in internal/external meetings to maintain project alignment.

Process Improvement

• Develop and maintain templates, tools, and SOPs.
• Lead or support initiatives focused on data automation and workflow enhancement (Manager level).

What You Bring

Education

• Bachelor’s degree in a scientific discipline (preferred).

Experience

• Strong background in a research or pharmaceutical environment with hands‑on clinical data management and clinical data review experience.
• CRO/Pharma industry experience preferred.
• Comfortable in customer‑facing roles; able to build and maintain strong stakeholder relationships.

Technical Skills

• Knowledge of CDISC standards (CDASH, SDTM, Controlled Terminology).
• Experience with common data formats (.xml, .xpt, sas7bdat, ASCII, .DAT, .xlsx).
• Proficiency in Microsoft Office; able to learn validated systems quickly.

Soft Skills

• Excellent communication, organizational, and leadership abilities.
• Ability to manage complex workloads under tight timelines.
• At Manager level: exceptional customer service and relationship‑building skills.

If you’re passionate about data integrity, collaboration, and advancing global health, we’d love to hear from you.

Apply today and make an impact with Charles River.

Seniority level

• Mid‑Senior level

Employment type

• Full-time

Job function

• Science

Benefits

• Medical insurance
• Vision insurance
• 401(k)
• Pension plan
• Paid paternity leave