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Clinical Data Associate Jobs in Reno, NV (NOW HIRING)

... data. * Assist in preparing responses to US regulatory authorities' questions within assigned timelines. * Recommend changes for clinical protocols for US regulatory compliance. * Recommend ...

... data. * Assist in preparing responses to US regulatory authorities' questions within assigned timelines. * Recommend changes for clinical protocols for US regulatory compliance. * Recommend ...

Collects and documents data acquired during the simulation procedure. Accurately inputs treatment ... Notifies appropriate clinical team members and documents of findings outside the normal range of ...

Collects and documents data acquired during the simulation procedure. Accurately inputs treatment ... Notifies appropriate clinical team members and documents of findings outside the normal range of ...

Payer Contract Specialist

Reno, NV · On-site

$31.19 - $43.68/hr

... reimbursement, clinical policies, credentialing, and resolving claims and other payer issues ... gather data, establish facts, draw valid conclusions and develop suitable recommendations. The ...

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Clinical Data Associate information

See Reno, NV salary details

$13

$38

$86

How much do clinical data associate jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for clinical data associate in Reno, NV is $38.84, according to ZipRecruiter salary data. Most workers in this role earn between $29.23 and $38.85 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

Which is better, CDM or SAS?

For a Clinical Data Associate, SAS is a widely used software for data analysis and reporting in clinical trials, while CDM (Clinical Data Management) refers to the overall process of collecting, cleaning, and managing clinical data, often using various tools including SAS. SAS skills are highly valued in the role, but understanding the broader CDM process is also important for effective data handling and compliance.

What's next after CRC?

After working as a Clinical Research Coordinator (CRC), professionals often advance to roles such as Clinical Data Associate, Clinical Trial Manager, or Regulatory Affairs Specialist. Gaining experience, certifications like CCRP, and developing skills in data management and regulatory compliance can facilitate career progression in clinical research.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What is the role of a clinical data associate?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of data from clinical trials. They review data for completeness, resolve discrepancies, and use database tools to support data integrity and regulatory compliance throughout the trial process.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

Do you need a degree to be a CRC?

A Clinical Data Associate (CDA) typically does not require a specific degree, but a background in life sciences, healthcare, or related fields is often preferred. Many employers value relevant certifications and experience with clinical data management tools. Educational requirements can vary by employer and job level.

Is CRA an entry level job?

A Clinical Data Associate (CDA) role is typically considered an entry-level position in clinical research, often requiring a bachelor's degree in a related field and some familiarity with data management tools. However, a Clinical Research Associate (CRA) role usually requires more experience and is considered a mid- to senior-level position, involving site monitoring and regulatory compliance. Entry-level roles may serve as a stepping stone toward CRA positions with additional experience and certifications.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Reno, NV? The most popular types of Clinical Data jobs in Reno, NV are:
What are popular job titles related to Clinical Data Associate jobs in Reno, NV? For Clinical Data Associate jobs in Reno, NV, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Reno, NV look for? The top searched job categories for Clinical Data Associate jobs in Reno, NV are:
What cities near Reno, NV are hiring for Clinical Data Associate jobs? Cities near Reno, NV with the most Clinical Data Associate job openings:
Medical Assistant

Medical Assistant

Nevada Advanced Pain Specialists

Reno, NV • On-site

$18 - $20/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday


Job description

Nevada Advanced Pain Specialists

Position Description

Overview

Position: Medical Assistant

Reports to: Clinical Supervisor/Practice Manager

Department: Clinical

Approved by: Dr. Patterson

Type of Relationship: Full-Time Employee

Exempt from Overtime: No

Schedule: Monday – Friday, 8am-5pm

Pay Range: $18.00 - $20.00 per hour starting

Benefits Eligibility: Eligible for standard company benefits package

***Must be willing to travel between office locations (Reno, Sparks and Carson City)***

Minimum Requirements for Candidates*

Education: High school diploma. Prefer a Bachelor’s or Associates degree in life science.

Certification: Prefer an active Certified Medical Assistant certification, but not required.

Work Experience: Prefer one year experience as a Medical Assistant in a Pain Management practice.

Setting: Must be able to work in an office setting with office and medical equipment.

Communication: Must be able to speak, read, and write English fluently.

*Candidate/employee/contractor must notify employer if any of these requirements can’t be met.

Essential Functions

1. Provide excellent customer service at all times.

2. Provide care and support to patients under the direction of the physician and/or mid level provider.

3. Perform timely, complete, and accurate work as it relates to each of the following specific job duties:

    1. Escort patients into and out of examine and waiting rooms.
    2. Greet and prepare patients for the provider. Provide patient mobility assistance, as necessary. Obtain and appropriately record into our computer systems vital signs and other appropriate information, such as height, weight, drug allergies, current medications, pain score, and presenting problem.
    3. Manage patient flow ensuring enough time for patient and family education. Screen, communicates and responds to patients needs appropriately within the scope of authority.
    4. Assist with diagnostic tests and clinical procedures. Prepare injectables for provider.
    5. Prepare, clean and sterilize instruments and maintain equipment; keep patient exam rooms clean and orderly; dispose of contaminated items according to facility requirements; anticipate provider’s needs for medications, supplies and equipment and plan accordingly.
    6. Document injectables, interactions, and vitals in patient’s medical record for every visit.
    7. Maintain clinical supplies.
    8. Schedule patient appointments, process referrals, prepare medical records and perform other clerical duties as needed.
    9. As needed or requested, collect urine samples on patients and deliver them to the laboratory for testing.
    10. When assigned to the front desk area, assist the front desk with greeting patients, checking in patients, and taking phone calls.
    11. As needed or requested, assist the scheduling team with confirming patient appointments, etc.

4. Provide reports and information as requested by practice management.

5. Other duties as assigned.

Other Functions

1. Contribute to the planning and delivery of patient focused care.

2. Adhere to all company policies and procedures.

3. Adhere to all Federal and State laws and regulations as it relates to this role, including all safety and health standards.

Competencies

1. Problem Solving - Identifies and resolves problems time efficiently; Gathers and analyzes information; Develops solutions; Uses reason.

  1. Oral Communication - Speaks clearly and persuasively; Listens and gets clarification when necessary; Responds informatively to questions; Demonstrates presentation skills; Participates in meetings.
  2. Written Communication - Writes clearly and concisely; Edits work; Presents data effectively; Able to read and interpret written information.
  3. Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently; Plans for additional resources; Sets goals and objectives; Organizes or schedules other people and their tasks; Formulates realistic action plans.
  4. Professionalism - Approaches others in a polite and tactful manner; Maintains composure and reacts well under pressure; Treats others with respect and consideration; Accepts responsibility for own actions; Follows through on commitments.
  5. Safety and Security - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.