2

No Experience Rn Clinical Data Abstractor Jobs in Tullahoma, TN

Travel Med Surg RN

Winchester, TN ยท On-site

$1.7K - $2.3K/wk

The right RN should have 1-2 years recent acute care experience. Read below for more requirements ... As a MedSurg RN, you will conduct patient assessments and prioritize data collection based on ...

Travel Med Surg RN

Winchester, TN ยท On-site

$1.7K - $2.3K/wk

The right RN should have 1-2 years recent acute care experience. Read below for more requirements ... As a MedSurg RN, you will conduct patient assessments and prioritize data collection based on ...

At least 2+ years' experience * Registered Nurse (RN) licensed * Valid TN license A Day One 401(k) ... A Dedicated Recruiter Who's Your Main Point of Contact NO PEGGY IN HOUSING, JIM IN TRAVEL, OR NANCY ...

Travel Med Surg RN

Winchester, TN ยท On-site

$1.7K - $2.3K/wk

Clinical experience within the last 2 years * Current State Licensure * Current Relevant ... Medical-Surgical - Registered Nurse About LeaderStat LeaderStat is a National staffing, recruiting ...

next page

Showing results 1-20

No Experience Rn Clinical Data Abstractor information

See Tullahoma, TN salary details

$17

$41

$64

How much do no experience rn clinical data abstractor jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for no experience rn clinical data abstractor in Tullahoma, TN is $41.46, according to ZipRecruiter salary data. Most workers in this role earn between $30.77 and $49.47 per hour, depending on experience, location, and employer.

What does a no experience RN clinical data abstractor do?

A No Experience RN Clinical Data Abstractor is a registered nurse who collects and analyzes clinical data from patient records, even if they are new to the field. Their main role is to ensure that important healthcare information is accurately documented and reported for quality improvement, compliance, and research. They use their nursing knowledge to interpret medical records and extract key data points, often working with electronic health record systems. Training is typically provided on the specific data abstraction protocols and software used by the employer. This position is ideal for nurses looking to transition from bedside care to a more data-driven, administrative role.

What are the key skills and qualifications needed to thrive as a no experience RN clinical data abstractor, and why are they important?

To thrive as a No Experience RN Clinical Data Abstractor, you need a registered nursing license, foundational clinical knowledge, and keen attention to detail. Familiarity with electronic health records (EHRs), clinical data abstraction software, and standardized coding systems like ICD-10 is typically required. Strong analytical thinking, organization, and effective communication skills help you interpret medical records accurately and collaborate with clinical teams. These skills ensure precise data extraction, regulatory compliance, and improved patient care outcomes.

What are some typical challenges faced by entry-level RN clinical data abstractors and how can they overcome them?

As an entry-level RN Clinical Data Abstractor, one common challenge is becoming familiar with various electronic medical record (EMR) systems and understanding complex clinical documentation. New abstractors may also need time to accurately interpret and extract relevant data while maintaining compliance with regulatory standards. Overcoming these challenges often involves comprehensive onboarding, mentorship from experienced team members, and ongoing training. Being proactive in asking questions and utilizing available resources can help you build confidence and proficiency in the role.

What are popular job titles related to No Experience Rn Clinical Data Abstractor jobs in Tullahoma, TN?

For No Experience Rn Clinical Data Abstractor jobs in Tullahoma, TN, the most frequently searched job titles are:

What job categories do people searching No Experience Rn Clinical Data Abstractor jobs in Tullahoma, TN look for?

The top searched job categories for No Experience Rn Clinical Data Abstractor jobs in Tullahoma, TN are:

What cities near Tullahoma, TN are hiring for No Experience Rn Clinical Data Abstractor jobs?

Cities near Tullahoma, TN with the most No Experience Rn Clinical Data Abstractor job openings:

Infographic showing various No Experience Rn Clinical Data Abstractor job openings in Tullahoma, TN as of August 2026, with employment types broken down into 4% As Needed, 77% Full Time, 13% Part Time, and 6% Contract. Highlights an 92% In-person, 2% Hybrid, and 6% Remote job distribution, with an average salary of $86,239 per year, or $41.5 per hour.

Clinical Research Nurse/Clinical Research Coordinator (RN/LPN)

CLINICAL TRIALS CENTER OF MIDDLE T

Belvidere, TN โ€ข On-site

$58K - $73K/yr

Other

Re-posted 14 days ago


Job description

Job Description
Job Description
Description:

We are seeking an experienced Clinical Research Nurse / Clinical Research Coordinator to join our growing team. This is a dual-role position that combines nursing responsibilities with hands-on study coordination. The ideal candidate is already experienced in sponsor-funded clinical research and can quickly integrate into an active research environment.


This position is ideal for a licensed nurse who enjoys both patient care and the operational aspects of clinical research. The candidate will serve as a study coordinator while also utilizing their nursing license to support clinical activities within the research clinic.
This is not an entry-level research position. Applicants should have previous experience coordinating sponsor-funded clinical trials and be comfortable independently managing study participants, sponsor expectations, and protocol requirements.

Responsibilities

- Coordinate Phase II-IV sponsor-funded clinical trials from screening through study completion.

- Conduct study visits in accordance with protocol requirements.

- Review medical history, concomitant medications, and adverse events with participants.

- Perform protocol-required clinical procedures within scope of licensure and delegation.

- Support investigational product preparation and accountability activities as permitted b y protocol

and site delegation.

- Assist with participant education and answer protocol-related medical questions within scope of practice.

- Complete source documentation, eSource, EDC, and query resolution accurately and promptly.

- Maintain study regulatory documentation and assist with essential document management.

- Communicate effectively with sponsors, CROs, monitors, laboratories, and study participants.

- Participate in monitoring visits, audits, and sponsor interactions.

- Serve as lead coordinator on assigned studies and help ensure enrollment, protocol compliance, and data quality goals are achieved.

- Collaborate closely with investigators, nurse practitioners, coordinators, regulatory staff, and leadership.

Requirements:

Qualifications

Required

- Current Tennessee RN or LPN license in good standing.

- Minimum of 2 years of sponsor-funded clinical research experience.

- Previous experience serving as a Clinical Research Coordinator.

- Strong understanding of ICH-GCP and FDA regulations.

- Experience with EDC systems and electronic source documentation.

- Excellent organizational skills and attention to detail.

- Ability to independently prioritize multiple studies and competing deadlines.

- Professional communication skills with patients, sponsors, CROs, and monitors.

Preferred

- Experience coordinating pulmonary, respiratory, internal medicine, and metabolic studies.

- Experience performing clinical assessments, specimen processing, ECGs, spirometry, or other

protocol-required procedures.

- ACRP or SOCRA certification (or willingness to obtain certification).


The right candidate is:

- Able to become productive quickly with minimal onboarding.

- Comfortable working independently while collaborating closely with the research team.

- Highly organized and able to manage multiple active studies simultaneously.

- Adaptable in a fast-paced environment where priorities can shift throughout the day.

- Committed to providing outstanding participant care while maintaining protocol compliance and data integrity.

- Proactive, dependable, and willing to take ownership of assigned studies.