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Clinical Study Manager Jobs in Tennessee (NOW HIRING)

McKesson Corporation

Study Coordinator

Nashville, TN · On-site

Will work closely with the physician principal investigator, manager of data operations, clinical trial sponsor and study team. * You will lead the execution of trials for the research team * You ...

Mckesson

Study Coordinator

Nashville, TN

Will work closely with the physician principal investigator, manager of data operations, clinical trialsponsorand study team. * You will leadthe execution of trials for the research team * You will ...

Integrated Resources INC

Sr.CRA

Nashville, TN

... clinical monitoring plan, ICH GCP, regulatory requirements, ensuring study completion on time and ... Reports directly to Manager, CRAs on general issues Reports to the Project Manager or Project Lead ...

McKesson

Study Coordinator

Nashville, TN

Will work closely with the physician principal investigator, manager of data operations, clinical trialsponsorand study team. * You will leadthe execution of trials for the research team * You will ...

McKesson

Study Coordinator

Nashville, TN

Will work closely with the physician principal investigator, manager of data operations, clinical trialsponsorand study team. * You will leadthe execution of trials for the research team * You will ...

micro1 AI

Medical Writing Manager

Knoxville, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Memphis, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Chattanooga, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Nashville, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Murfreesboro, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Clarksville, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

LabConnect

Biospecimen Project Manager

Johnson City, TN · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

Review nonclinical and clinical study protocols and service providers' scope of work documents for ... Manage specimen metadata discrepancies and ensure resolution * Submit specimens for analytical ...

LabConnect

Biospecimen Project Manager

Johnson City, TN · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

Review nonclinical and clinical study protocols and service providers' scope of work documents for ... Manage specimen metadata discrepancies and ensure resolution * Submit specimens for analytical ...

LabConnect

Manager, Proposals

Johnson City, TN · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

Oversee the clinical study quote submission process and timelines to exceed customer expectations ... Provide mentoring, guidance, and training to Proposal Management team members relevant to their ...

LabConnect

Biospecimen Project Manager

Johnson City, TN · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

Review clinical study protocols and service providers' scope of work documents for sample handling ... Create and manage project plans, templates and framework for consistent execution across vendors ...

micro1 AI

Medical Billing Specialist

Chattanooga, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Billing Specialist

Nashville, TN · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

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All JobsClinical Study JobsClinical Study Manager JobsClinical Study Manager Jobs in Tennessee

Clinical Study Manager information

See Tennessee salary details

$26

$56

$87

How much do clinical study manager jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical study manager in Tennessee is $56.74, according to ZipRecruiter salary data. Most workers in this role earn between $46.06 and $63.94 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

What are the most commonly searched types of Clinical Study jobs in Tennessee?

The most popular types of Clinical Study jobs in Tennessee are:

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

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

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

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

What cities in Tennessee are hiring for Clinical Study Manager jobs?

Cities in Tennessee with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study 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, with an average salary of $118,021 per year, or $56.7 per hour.

Clinical Research Assistant (30795)

GI Alliance

Germantown, TN • On-site

$27 - $29/hr

Full-time

Re-posted 8 hours ago

GI Alliance rating

6.4

Company rating: 6.4 out of 10

Based on 69 frontline employees who took The Breakroom Quiz

642nd of 887 rated healthcare providers

Job description

JOB TITLE: Research Assistant
FSLA STATUS: Exempt
POSITION SUMMARY:
Experienced Medical Assistant or Research Assistant needed to contribute to Urology Conrad Pearson growing research department. Research Assistant (RA) roles often transition to Clinical Research Coordinator (CRC) roles and open the door to many other career opportunities within the industry. Research Assistants support the Clinical Research Team with subject recruitment, diagnostic testing, laboratory specimen collection, communications with patients, study sponsors, and investigators, and other interesting research related roles.
You will work closely with our Study Coordinators, Clinical Research Director, Principal Investigators (PI) and Sub-Investigators (Sub-Is) on various clinical research studies.
JOB RELATIONSHIPS:
  • Reports to the Director of Clinical Research, VP of Clinical Research, Market President, and all the physicians at Urology Austin
  • Able to collaborate with experienced patient navigators, IT, and data management teams

ROLE QUALIFICATIONS: (experience, education, and skills)
  • Must be willing to gain a thorough knowledge and follow strict adherence of all clinical study protocols.
  • Develop an understanding of and demonstrate Good Clinical Practices (GCPs), learn and comply with all FDA clinical trial and IRB rules and regulations
  • Must have > 1 year experience as a medical assistant or research assistant.
  • Urology based clinical experience preferred
  • Should possess or develop proficiency in computer software use, including Microsoft Office, EMR and Practice Management systems, and study specific EDC and IVRS systems
  • Effective time management and the ability to prioritize work
  • Excellent communication skills and the ability to interact with all levels of management, staff, and physicians in person, virtually, and in writing
  • Ability to be flexible with the day-to-day job requirements to facilitate a successful workflow in clinic

ESSENTIAL JOB RESPONSIBLITIES:
  • Review and follow Urology Austin Standard Operating Procedures
  • Read and understand specific requirements of each study protocol and informed consent form
  • Works with study coordinators and other research team members to complete protocol specific procedures and documentation
  • Assists in clinic and protocol administration duties including but not limited to:
    • Explain the purpose, risks, and benefits of clinical trial participation
    • Screen potential candidates in a timely and accurate manner
    • Ensure that study patients understand the information presented and agree to the protocol requirements
    • Obtain and maintain consent of patients prior to any study-related procedures being performed and with the highest ethical standards
    • Provide instructions to patients to ensure proper protocol compliance
    • Distribute study medications in compliance with protocol randomization requirements
    • Learn and understand lab procedures and obtain and process study related lab specimens according to the study specific manuals (lab and procedural)
    • Use approved source documents; obtain protocol-specific data to complete and maintain source documents and case report forms (including electronic data capture - EDC) in accordance with applicable regulations and sponsor requirements
    • Perform study-specific readings and measurements including but not limited to:
  • Vital signs
  • ECG
  • Urine Pregnancy Test
  • Uroflow, TRUS, urinalysis, cystoscopy
  • Photography and videography
  • Reports irregular readings and measurements to Investigator and Lead Study Coordinator
  • Package and ship laboratory specimens to study-specific destinations
  • Complete applicable training requirements and ongoing education as required
  • Maintain certifications in, and continually update knowledge of, FDA, GCP, ICH, federal and state regulations, etc.
  • Communicate with and support patients and their families as necessary.
  • Work with the EMR and data management systems to complete EDC, eCRFs, find patients, maintain records
  • Effectively communicate with potential candidates for trials and collect metrics to track progress
  • Must have or gain knowledge of relevant software/programs

  • Work closely with IRB and study sponsors, PIs and Sub-Is. Attend necessary meetings and calls
  • Assist with the development of source documents and phone screen tools
  • Manage ancillary supply inventory and assist with drug accountability
  • Maintain HIPAA compliant communication and confidentiality, at all times
  • Participate in site visits (site initiation visits, interim monitoring visits, close-out visits, etc.
  • Assist study coordinators with necessary study close-out procedures and documentation
  • Performs other duties as assigned

Performance Requirements:
Knowledge
  • Knowledge of health care field; medical practice clinical and administrative systems, departments, and practices, including clinical financial policies and reimbursement payment requirements.
  • Understanding of medical terminology.

Skills
  • Ability to use multi-line phone systems and basic computer systems.
  • Interpersonal and communication both with internal staff and external customers.
  • Skill in evaluating and implementing study protocols and budgets.
  • Skill in reading medical chart terminology.
  • Time Management.

Abilities
  • Ability to communicate effectively with patients, staff, and external contacts via phone, in person, and through electronic mail.
  • Elicit appropriate information for patients to clinic staff.
  • Ability to read and understand information and ideas presented in writing.
  • Ability to apply general rules to specific problems to produce answers that make sense - deductive reasoning.

Reporting to this position: No direct reports at this time, can change as department grows
Physical Demands and Work Environment:
The physical demands and work environment characteristics described here are the representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions:
  • Physical demands: Involves sitting approximately 90 percent of the day, walking or standing for the remainder. Work may require stooping and bending to access files, supplies, mobility to complete errands, and lifting up to 20 pounds.
  • Work environment: Primarily office setting. Noise level in the work environment is usually moderate. Clean, well-lighted office environment.

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