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Clinical Project Associate Jobs in Bethpage, TN (NOW HIRING)

IQVIA

Senior Project Lead Field Director

Nashville, TN

$200K - $240K/yr

Associate's degree or higher. * 8+ years of leadership experience within nursing services, patient ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

Icon plc

Senior CRA

Nashville, TN · On-site

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

Integrated Resources INC

Sr.CRA

Nashville, TN

The SCRA will provide expert advice, guidance and general supervision to clinical monitoring team activities for designated projects, and to monitor specified sites to ensure quality and integrity of ...

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Clinical Project Associate information

See Bethpage, TN salary details

$12

$29

$52

How much do clinical project associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical project associate in Bethpage, TN is $29.85, according to ZipRecruiter salary data. Most workers in this role earn between $20.00 and $39.38 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a clinical project associate?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What cities near Bethpage, TN are hiring for Clinical Project Associate jobs?

Cities near Bethpage, TN with the most Clinical Project Associate job openings:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Bethpage, TN as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 21% Part Time, 6% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $62,093 per year, or $29.9 per hour.

Senior Clinical Research Associate

Luminate Medical

Nashville, TN • Remote

Full-time

Re-posted 6 days ago

Job description

Shape the Future of Cancer Treatment at Luminate 
 

Luminate is on a mission to change the way we experience cancer care. We design and build products which revolutionize the patient experience of cancer treatment by eliminating the financial, physical, and temporal side effects of anti-cancer therapy. Our development programs include enabling at-home lab draws and infusions, preventing peripheral neuropathy, and preventing hair loss caused by chemotherapy. We’ve proven our ability to bring technologies to patients, with several active clinical trials around the world.  

We’re  looking for a Senior Clinical Research Associate to
play a key role in supporting the execution of pivotal clinical trials. Working closely with our Director of Clinical Operations, you will be the main point of contact in ensuring clinical trial execution at the sites is operating in accordance with GCP and study timelines. 

 
Working at Luminate 
 

  • This is a key hire within the Clinical Operations Department, at a rapidly growing startup. You will have an opportunity to manage components of start-up, execution, and close-out of key pivotal clinical trials 
  • You’ll be hands-on with the devices and with managing clinical sites as a representative of the sponsor company 
  • Closely collaborate with a team that trusts your judgment and empowers you to act 
  • Be part of a company that’s scaling up, offering ample opportunity to step up as trials and device portfolio continue to expand 


What You Will Do:
 

  • Act as the subject matter expert for Luminate Medical devices, serving as the primary point of contact between sponsor and site staff. 
  • Manage and maintain essential study documents in compliance with sponsor requirements, study-specific processes, and Luminate SOPs. 
  • Collaborate with internal and external clinical teams to support all phases of clinical trials, including study start-up, site initiation visits (SIVs), trial execution, and close-out. 
  • Perform weekly check-ins with clinical sites to track progress, address issues, and provide ongoing support. 
  • Contribute to departmental projects and initiatives, ensuring timely and high-quality deliverables. 
  • Proactively identify and escalate training needs, project updates, quality concerns, and timeline risks to the clinical team. 


Personal Attributes – The Ideal Candidate Is:
 

  • Communicative: Proficient in written and verbal communication and collaboration skills. You are able to identify appropriate communication channels for problems and concerns.  
  • Self-Driven: You have a sense of urgency in your work and thrive when taking responsibility for tasks. Proactive thinker and problem-solver with an enthusiasm to learn new concepts and a growth mindset. 
  • Attention to Detail: Understands and adheres to company policies and procedures. Understands and adheres to all external standards, and applicable regulations. Ability to work under strict guidelines, competing priorities, and immediate requests.  
  • Professional: Displays a neat, clean, and professional appearance at all times.  
     

Requirements – The Ideal Candidate Must Have:
 

  • Bachelor’s degree in Life Sciences or a related field. Master’s degree preferred. 
  • 3–5+ years of hands-on experience within the medical device and/or pharmaceutical industry  
  • Prior experience with Trial Master File (TMF) management 
  • Prior experience and proficiency in utilizing Electronic Data Capture (EDC) systems 
  • Deep understanding of GCP, ISO 14155, and FDA regulations for medical devices 
  • Willingness and ability to travel 30-40% during active clinical trials period 


Advantages – It Would be Advantageous to Have:
 

  • Experience within biotech start-ups 
  • Experience working for a Sponsor company  
  • Experience in the Oncology therapeutic area. 
  • Strong site relationship management skills 
  • A passion for working in small, entrepreneurial environments where everyone wears multiple hats. 

 
Don’t have all of these requirements?
 

Some people are less likely to apply for a role unless they are 100% qualified. Your experience, skills and passion will set you apart - tell us what you have learned and achieved, whether personal or work-related! With the right mindset, many of the skills above can be learned on the job. If this role excites you, don’t let the description hold you back!