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Clinical Data Management Associate Jobs (NOW HIRING)

VIVA USA INC

Clinical Data Management

Palo Alto, CA · On-site

Experience in oncology clinical research, EPIC medical record experience, data entry PHYSICAL REQUIREMENTS: Sitting in place at computer for long periods of time with extensive keyboarding/dexterity.

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

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Clinical Data Management Associate information

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$13

$38

$86

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

As of Jul 21, 2026, the average hourly pay for clinical data management associate 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.

Which is better, CDM or SAS?

For a Clinical Data Management Associate, SAS is a widely used statistical software for data analysis and reporting, while CDM refers to the role of managing clinical data, often involving tools like electronic data capture systems. Both are important in clinical trials, but SAS skills are highly valued for data analysis tasks, whereas CDM focuses on data collection, validation, and database management.

Is clinical data management a good career?

Clinical Data Management Associate roles involve collecting, cleaning, and maintaining clinical trial data, requiring knowledge of databases and regulatory standards. It offers opportunities for growth in the pharmaceutical and healthcare industries, with a demand for strong analytical and technical skills. The field provides a stable career path with potential for advancement and specialization.

What does a clinical data associate do?

A Clinical Data Management Associate is responsible for collecting, cleaning, and maintaining clinical trial data to ensure accuracy and compliance. They use data management tools and work closely with research teams to support the integrity of trial results and may require knowledge of regulatory standards like GCP and data validation techniques.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically an entry-level to mid-level position in clinical trials, often requiring a bachelor's degree in a related field and some experience in clinical research or monitoring. Entry-level CRAs usually undergo training and may need certifications such as SOCRA or ACRP to advance in the role.

What is the difference between Clinical Data Management Associate vs Clinical Data Coordinator?

AspectClinical Data Management AssociateClinical Data Coordinator
ResponsibilitiesData entry, validation, database management, ensuring data qualityOversees data collection, manages databases, coordinates data flow between teams
Required SkillsAttention to detail, knowledge of clinical data systems, basic understanding of regulationsStrong organizational skills, data management experience, communication skills
Work EnvironmentClinical research labs, CROs, pharmaceutical companiesClinical trial sites, research organizations, CROs
Common UsageEntry to mid-level data roles in clinical trialsData oversight and coordination roles in clinical studies

The Clinical Data Management Associate focuses on data entry, validation, and database management, ensuring data accuracy. The Clinical Data Coordinator oversees data collection and flow, coordinating between teams. Both roles require similar skills and work environments but differ in scope and responsibilities.

What cities are hiring for Clinical Data Management Associate jobs? Cities with the most Clinical Data Management Associate job openings:
What are the most commonly searched types of Clinical Data Management jobs? The most popular types of Clinical Data Management jobs are:
What states have the most Clinical Data Management Associate jobs? States with the most job openings for Clinical Data Management Associate jobs include:
Clinical Data Management Associate jobs near you
Clinical Data Management

Clinical Data Management

VIVA USA INC

Palo Alto, CA • On-site

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

JOB PURPOSE:
Enter data from a source document into a computer system and verify entries for accuracy and completeness. Maintain complex databases and develop tools and guidelines for data collection and integrity. Work is performed by exercising independent judgment and initiative in performing tasks.
CORE DUTIES:
Establish complex record-keeping procedures, including cross-indexing by several factors and the designing of necessary forms.
Maintain existing databases and develop guidelines to ensure data integrity; may integrate data from several sources.
Identify and select usable data from extremely subtle and complex data patterns, applying practical understanding.
Utilize computer applications to manipulate and report complex data.
Develop new tools to assist with data collection and analysis.
Work with data providers to discuss and clarify data ambiguities, inconsistencies etc.
Perform audits of own work or that of others to ensure conformance with established procedure.
Select and apply appropriate formulas, computer programs, or applications depending on data content.
May provide administrative support.
MINIMUM REQUIREMENTS:
Education & Experience:
High school diploma, G.E.D., or equivalent and three years of relevant experience or a combination of education and relevant experience.
Knowledge, Skills and Abilities:
Strong clerical, interpersonal, and organizational skills.
Excellent computer skills.
Ability to exercise judgment and employ basic reasoning skills.
Strong attention to detail.
Required experience:
Approximately 1 year
Top 3 requirements to hire:
Experience in oncology clinical research, EPIC medical record experience, data entry
PHYSICAL REQUIREMENTS:
Sitting in place at computer for long periods of time with extensive keyboarding/dexterity.
Occasionally use a telephone.
Rarely writing by hand.
Notes:
Onsite 5-days per week
VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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