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Clinical Research Data Jobs (NOW HIRING)

Dana-Farber Cancer Institute

The Research Data Specialists will support the clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and ...

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$13

$24

$40

How much do clinical research data jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for clinical research data in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

How to become a clinical research data analyst?

To become a clinical research data analyst, typically a bachelor's degree in a related field such as life sciences, statistics, or data management is required. Gaining experience with data analysis tools like SAS, R, or SQL, and understanding clinical trial processes and regulations, can improve job prospects. Certifications in clinical data management or related areas may also be beneficial.

What is the difference between Clinical Research Data vs Clinical Research Coordinator?

AspectClinical Research DataClinical Research Coordinator
Primary RoleManaging and analyzing data collected during clinical trialsOverseeing trial operations, patient recruitment, and site management
Required SkillsData management, statistical analysis, familiarity with EDC systemsPatient interaction, study protocol adherence, organizational skills
Work EnvironmentData centers, research labs, clinical trial sitesClinical sites, hospitals, research facilities
CertificationsOften requires knowledge of GCP, data management certificationsGCP certification, clinical research training

Clinical Research Data specialists focus on managing and analyzing data from clinical trials, while Clinical Research Coordinators handle the operational aspects of conducting trials. Both roles are essential in the clinical research process but differ in responsibilities and skill sets.

What does a clinical research data specialist do?

A clinical research data specialist manages and analyzes data collected during clinical trials to ensure accuracy, completeness, and compliance with regulatory standards. They often use data management tools like electronic data capture (EDC) systems and collaborate with research teams to support study integrity and reporting.

What is clinical research data?

Clinical research data refers to the information collected during clinical trials and research studies involving human participants. This data includes patient demographics, medical histories, laboratory results, treatment outcomes, and adverse events, among other variables. The purpose of collecting and analyzing clinical research data is to evaluate the safety and effectiveness of medical interventions, drugs, or devices. Proper management and integrity of this data are critical for regulatory compliance and advancing medical knowledge.

Is clinical data analysis a good career?

Clinical research data analysis involves managing and interpreting data from clinical trials, requiring skills in statistics, data management, and familiarity with tools like SAS or R. It offers opportunities in healthcare, pharmaceuticals, and biotech industries with steady demand and potential for career growth. Certification and attention to regulatory standards can enhance job prospects.

What are the common challenges faced by professionals working in Clinical Research Data roles?

Professionals in Clinical Research Data often encounter challenges such as maintaining data integrity, ensuring compliance with strict regulatory requirements, and managing large volumes of complex data from multiple sources. They must be detail-oriented to detect discrepancies and ensure accurate data entry, while also collaborating closely with clinical teams and statisticians to interpret findings. Additionally, keeping up with evolving data management technologies and standards is crucial for career growth and continued effectiveness in the role.

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

To thrive as a Clinical Research Data Specialist, you need a solid understanding of clinical research protocols, data management practices, and typically a degree in life sciences or a related field. Experience with electronic data capture (EDC) systems, statistical analysis software (such as SAS or SPSS), and knowledge of regulatory requirements like GCP are highly valued. Attention to detail, problem-solving abilities, and strong communication skills help ensure high-quality data and effective collaboration with research teams. These skills are crucial for maintaining data integrity, supporting regulatory compliance, and ensuring the success of clinical trials.

Which clinical research jobs pay the most?

Senior roles in clinical research, such as Clinical Research Directors and Principal Investigators, tend to have the highest salaries, often exceeding six figures. These positions typically require extensive experience, advanced degrees, and certifications like CCRP or RAC, and involve overseeing multiple studies or teams. Compensation varies based on location, organization, and level of responsibility.
More about Clinical Research Data jobs
What cities are hiring for Clinical Research Data jobs? Cities with the most Clinical Research Data job openings:
What are the most commonly searched types of Clinical Research Data jobs? The most popular types of Clinical Research Data jobs are:
What states have the most Clinical Research Data jobs? States with the most job openings for Clinical Research Data jobs include:
Clinical Research Data jobs near you
Infographic showing various Clinical Research Data job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Coordinator

ELEVATE CLINICAL RESEARCH, INC.

Mcallen, TX • On-site

$17.50 - $23.25/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

About Company:

Elevate Clinical Research is a mission‑driven organization expanding access to high‑quality clinical trials across Texas, Louisiana, Illinois, Maryland, Kansas, and growing. We exist to bring research closer to the communities that need it most, delivering compassionate patient care, operational excellence, and trustworthy data that advances medicine.

At Elevate, your work has real impact. Every role contributes directly to improving health outcomes and bringing new therapies to life. We hire people who care deeply about patients, believe in doing things the right way, and want to grow with a company that’s expanding nationwide.

What We Value

  • Patients first in every decision and interaction

  • Access, equity, and bringing research to underserved communities

  • High‑quality, compliant, reliable study execution

  • Purpose‑driven growth and opportunities for advancement

  • Supportive teams who communicate, collaborate, and care

Why People Join Us

  • A mission that matters

  • Clear, structured onboarding

  • Leadership that listens and supports

  • Career growth as we expand into new states

  • A culture built on integrity, teamwork, and accountability

Join Elevate and help build a patient‑centered research network that’s changing what clinical trials can look like for communities across the country.

About the Role:

The Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution and management of clinical trials within healthcare settings. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory requirements and institutional policies. The CRC serves as a liaison between investigators, study sponsors, and participants, facilitating effective communication and smooth study progression. By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to advancing medical knowledge and improving patient care through the rigorous conduct of clinical research.

Minimum Qualifications:

  • Bachelor’s degree in a health-related field such as Nursing, Life Sciences, or Public Health.
  • At least 2 years of experience coordinating clinical research studies or trials.
  • Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.
  • Familiarity with clinical research documentation, including informed consent forms and case report forms.
  • Strong organizational skills and attention to detail to manage multiple study activities simultaneously.

Preferred Qualifications:

  • Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).
  • Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
  • Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes.
  • Previous experience in patient recruitment and retention strategies for clinical studies.
  • Master’s degree in Clinical Research, Public Health, or a related discipline.

Responsibilities:

  • Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.
  • Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.
  • Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.
  • Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties.
  • Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly.

Skills:

The required skills such as clinical trials coordination, regulatory document management, and patient recruitment are essential for ensuring that studies are conducted efficiently and ethically. Clinical monitoring and trial management skills enable the coordinator to oversee study progress and maintain compliance with protocols and regulations. Proficiency in clinical research and clinical practice allows the coordinator to understand medical terminology and patient care considerations, facilitating effective communication with healthcare providers and participants. Preferred skills like experience with electronic data systems and advanced regulatory knowledge enhance the ability to manage complex data and navigate regulatory landscapes. Together, these skills support the daily responsibilities of maintaining study integrity, safeguarding participant safety, and contributing to the advancement of healthcare research.