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Trials Manager Jobs in Tennessee (NOW HIRING)

KidStrong West Nashville

Sales Manager

Burns, TN · On-site

$18 - $24/hr

Following up with families after trials and converting them into memberships. * Explaining the KidStrong program and answering parent questions. * Managing leads and member information in CRM systems ...

KidStrong

Sales Manager

Burns, TN · On-site

$18 - $24/hr

Following up with families after trials and converting them into memberships. * Explaining the KidStrong program and answering parent questions. * Managing leads and member information in CRM systems ...

The US Oncology Network

Human Resources Manager

Nashville, TN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The practice conducts clinical trials through their affiliation with Sarah Cannon Research Institute (SCRI), a global leader in oncology research that has been offering and managing clinical trials ...

The US Oncology Network

Human Resources Manager

Nashville, TN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The practice conducts clinical trials through their affiliation with Sarah Cannon Research Institute (SCRI), a global leader in oncology research that has been offering and managing clinical trials ...

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Trials Manager information

What are the key skills and qualifications needed to thrive as a trials manager, and why are they important?

To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.

What is a trials manager?

Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.

What are the main challenges a trials manager faces when coordinating multi-site clinical trials?

As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.

What is the difference between Trials Manager vs Clinical Research Coordinator?

CriteriaTrials ManagerClinical Research Coordinator
Required CredentialsBachelor's degree, experience in trial management, knowledge of regulationsBachelor's degree, clinical research experience, regulatory knowledge
Work EnvironmentOversees multiple trials, manages teams, coordinates with sponsorsHandles daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.

What are popular job titles related to Trials Manager jobs in Tennessee?

For Trials Manager jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Trials Manager jobs in Tennessee look for?

The top searched job categories for Trials Manager jobs in Tennessee are:

Trials Manager jobs near you
Infographic showing various Trials Manager job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

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

CLINICAL TRIALS CENTER OF MIDDLE T

Franklin, TN • On-site

$68K - $85K/yr

Full-time

Re-posted 6 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.