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Associate Clinical Data Manager Jobs (NOW HIRING)

innovitusa

Clinical Data Manager

Jackson, MS · On-site

The candidate will manage, implement, maintain and support clinical databases related pre-market clinical studies/registries. The candidate will have an understanding of data review, oversight, and ...

New

Rho Inc

Clinical Data Manager

As our next Clinical Data Manager, you will have the opportunity to work closely with the multidisciplinary project team across the life cycle of the project to ensure data management is thoughtfully ...

Collabera

Clinical Data Manager

Irvine, CA · On-site

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of Extension) Employment Type: W2 Contingent Worker SUMMARY OF POSITION: As a key member of the Global ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA · On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

CTI

Clinical Data Manager

Covington, KY · On-site +1

JOB PURPOSE / SUMMARY This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA · On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA · On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

Viz.ai

Clinical Data Manager

$127.17K - $182.86K/yr

This position plays a critical role in driving Viz's Evidence Generation strategy by managing the data life-cycle for clinical research and quality improvement studies. This role requires expertise ...

Lancesoft

Clinical Data Manager

South San Francisco, CA · On-site

$82 - $85/hr

Oversee collection and validation of clinical data Develop and manage clinical databases Ensure data quality and compliance with regulatory requirements Collaborate with cross-functional teams for ...

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How much do associate clinical data manager jobs pay per hour?

As of May 28, 2026, the average hourly pay for associate clinical data manager in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Clinical Data Manager, and why are they important?

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an Associate Clinical Data Manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.

What does an Associate Clinical Data Manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.
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Associate Clinical Data Manager jobs near you
Infographic showing various Associate Clinical Data Manager job openings in the United States as of May 2026, with employment types broken down into 84% Full Time, 6% Part Time, 4% Temporary, and 6% Contract. Highlights an 86% In-person, 4% Hybrid, and 10% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.
Clinical Data Manager/Clinical Data Reviewer

Clinical Data Manager/Clinical Data Reviewer

Charles River Laboratories

Manhattan, NY • Remote

Full-time

Medical, Vision, Retirement

Posted 7 days ago

Charles River Laboratories rating

8.1

Company rating: 8.1 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

31st of 70 rated pharmaceutical

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 #J-18808-Ljbffr

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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