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Edc Jobs in Tennessee (NOW HIRING)

PSI CRO

Clinical Study Coordinator

Cleveland, TN · On-site

Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to ...

PSI CRO

Clinical Study Coordinator

Cleveland, TN · On-site

Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to ...

Parsons

Deputy Project Manager

Kingsport, TN

Deputy Project Manager - Holston EDC Project Parsons is looking for an amazingly talented Project Manager to join our team! In this role, you will assist in the leadership and delivery of a multi ...

New

Honorhealth

$23.50 - $31.50/hr

Other Strong writing and computer skills, including, MS Word, Excel, Access, EDC ( electronic data capture) - Preferred Licenses and Certifications * Basic Life Support (BLS) - Required * Clinical ...

HCA Healthcare

Research Data Coordinator

Nashville, TN · On-site

Jump-start your career as a Research Data Administrative Assistant today with HCA Healthcare. Job Summary and Qualifications The Data Coordinator is responsible for EMR data abstraction, EDC data ...

HCA Healthcare

Research Data Coordinator

Franklin, TN · On-site

Jump-start your career as a Research Data Administrative Assistant today with HCA Healthcare. Job Summary and Qualifications The Data Coordinator is responsible for EMR data abstraction, EDC data ...

Care Access

Clinical Research Coordinator II

Memphis, TN · On-site

$23.50 - $31.25/hr

Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords) The Expertise Required * Ability to understand ...

HCA Healthcare

Research Data Coordinator

Lebanon, TN · On-site

Jump-start your career as a Research Data Administrative Assistant today with HCA Healthcare. Job Summary and Qualifications The Data Coordinator is responsible for EMR data abstraction, EDC data ...

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How much do edc jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for edc in Tennessee is $22.81, according to ZipRecruiter salary data. Most workers in this role earn between $18.56 and $26.20 per hour, depending on experience, location, and employer.

What are some common challenges faced by EDC (Electronic Data Capture) professionals in clinical research, and how can they be managed?

Professionals working with Electronic Data Capture (EDC) systems in clinical research often encounter challenges such as ensuring data accuracy, maintaining regulatory compliance, and managing system updates. These challenges can be managed by staying up-to-date with industry regulations, participating in ongoing training, and collaborating closely with clinical teams to streamline data entry processes. Regular communication with IT and data management teams is also crucial to address technical issues promptly and ensure smooth workflows.

What are the key skills and qualifications needed to thrive as an EDC (Electronic Data Capture) Specialist, and why are they important?

To thrive as an EDC Specialist, you need a solid understanding of clinical data management, data integrity principles, and experience with electronic data capture in clinical trials, often supported by a degree in life sciences or related fields. Familiarity with EDC systems like Medidata Rave or Oracle InForm, and certifications such as CDISC or GCP, are typically required. Attention to detail, problem-solving, and strong communication skills help you effectively collaborate with clinical teams and ensure high-quality data collection. These skills are crucial for accurate, compliant data management, which underpins the success of clinical research projects.

What are EDCs?

EDC stands for 'Everyday Carry.' In the context of jobs, an EDC typically refers to the essential tools, gadgets, or items that someone carries daily to be prepared for work or emergencies. This can include multitools, flashlights, pocket knives, pens, and other items tailored to the individual's profession or needs. People in security, law enforcement, medical fields, or even office environments often have different EDC items. The concept emphasizes practicality, preparedness, and efficiency in daily tasks.
What are popular job titles related to Edc jobs in Tennessee? For Edc jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Edc jobs in Tennessee look for? The top searched job categories for Edc jobs in Tennessee are:
Edc jobs near you

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

CLINICAL TRIALS CENTER OF MIDDLE T

Franklin, TN • On-site

$68K - $85K/yr

Full-time

Posted 7 days ago

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.