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Clinical Data Manager Jobs in Rio Rancho, NM (NOW HIRING)

Clinical Psychologist

Albuquerque, NM

$85K - $118K/yr

Clinical Psychologist - Veteran Disability Assessments We are seeking a dedicated Clinical ... Strong analytical skills to review medical records and assessment data. * Excellent time management ...

Clinical Psychologist

Albuquerque, NM · On-site

$85K - $118K/yr

Clinical Psychologist - Veteran Disability Assessments We are seeking a dedicated Clinical ... Strong analytical skills to review medical records and assessment data. * Excellent time management ...

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Clinical Data Manager information

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How much do clinical data manager jobs pay per hour?

As of Jul 8, 2026, the average hourly pay for clinical data manager in Rio Rancho, NM is $53.77, according to ZipRecruiter salary data. Most workers in this role earn between $42.50 and $63.99 per hour, depending on experience, location, and employer.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What degree do you need to be a Clinical Data Manager?

A Clinical Data Manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or health informatics. Many employers prefer candidates with a master's degree or additional certifications in clinical research or data management. Strong knowledge of database tools and regulatory standards is also important for the role.

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

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data management do?

A clinical data manager is responsible for designing, implementing, and maintaining systems to collect, clean, and analyze data from clinical trials. They ensure data accuracy, integrity, and compliance with regulatory standards using tools like electronic data capture (EDC) systems. This role requires attention to detail, knowledge of Good Clinical Practice (GCP), and often involves collaboration with research teams and data analysts.

What Does a Clinical Data Manager Do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills and familiarity with clinical trial software such as EDC systems.

What is the role of a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, implementing, and maintaining systems to collect, manage, and ensure the quality of clinical trial data. They oversee data validation, perform data cleaning, and collaborate with study teams to ensure accurate and compliant data collection using tools like electronic data capture (EDC) systems. Their role is essential for supporting regulatory submissions and ensuring trial integrity.
What job categories do people searching Clinical Data Manager jobs in Rio Rancho, NM look for? The top searched job categories for Clinical Data Manager jobs in Rio Rancho, NM are:
What cities near Rio Rancho, NM are hiring for Clinical Data Manager jobs? Cities near Rio Rancho, NM with the most Clinical Data Manager job openings:
Infographic showing various Clinical Data Manager job openings in Rio Rancho, NM as of July 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 84% In-person, 6% Hybrid, and 10% Remote job distribution, with an average salary of $111,846 per year, or $53.8 per hour.
Clinical Research Supervisor

Clinical Research Supervisor

University of New Mexico

Albuquerque, NM • On-site

Other

Re-posted 5 days ago


University Of New Mexico rating

8.5

Company rating: 8.5 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

70th of 546 rated colleges and universities


Job description

The University of New Mexico's Center for Memory & Aging is seeking a Clinical Research Supervisor for the newly funded New Mexico Alzheimer's Disease Research Center (NM ADRC). While the term end is 2025, the grant is expected to be funded through at least 2029.  https://hsc.unm.edu/research/centers-programs/nmadrc/
The Center for Memory & Aging (CMA) at UNM is funded primarily from National Institute of Health (NIH) grant mechanisms, our main projects involve longitudinal study of older participants with and without cognitive problems, including collection of MRIs, cognitive, neurological, and biospecimen data. Currently all our research studies work with older adults, ages 50 and above. The Center for Memory & Aging is a growing center with a focus on research in Alzheimer's and related dementias. We have a long record of continued research funding.
The CMA is seeking a self-starter, motivated, candidate to coordinate the day-to day activities for research studies. The ideal candidate will have experience coordinating research clinical trials or participant-based research studies. Understanding and training in Human Research as well as Good Clinical Practice will be required.
The responsibilities will include recruiting and scheduling patients for ongoing research studies, ensuring protocol adherence for each study, and maintaining accurate records. Duties also include the collection, compilation, and management of study data. The individual in this position must have strong interpersonal and communication skills and the ability to work effectively with a wide range of people in a diverse community, particularly older adults with cognitive difficulties and their families. This employee will work with confidential information and data, work directly with patients and physicians, to schedule and coordinate research appointments and examinations. Position may involve sporadic travel for recruitment events, generally within the Albuquerque area.  
In addition to the above, the position may include assisting with the coordination of add on studies may include EEG, EKG, PET scan and other medical procedures which this position would help to coordinate. Interest or experience in other medical procedures would be an asset.


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