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Clinical Research Associate Jobs in Baton Rouge, LA

State of Louisiana

RESEARCH ASSOCIATE

Baton Rouge, LA · On-site

$50K/yr

About this Job Northwestern State University seeks qualified applicants for the position of Research Associate. This position is in the Preservation Technical Services Division of Northwestern State ...

State of Louisiana

RESEARCH ASSOCIATE

Baton Rouge, LA · On-site

$50K/yr

Northwestern State University Opening Date: 06/02/2026 About this Job Northwestern State University seeks qualified applicants for the position of Research Associate. This position is in the ...

Louisiana State University

Transient

Baton Rouge, LA · On-site

The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling both focused research and translational science. Research at Pennington is supported broadly by ...

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Clinical Research Associate information

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$9

$32

$54

How much do clinical research associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical research associate in Baton Rouge, LA is $32.27, according to ZipRecruiter salary data. Most workers in this role earn between $22.64 and $41.30 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, 2% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $67,112 per year, or $32.3 per hour.

Limited Term Clinical Research Coordinator

DelRicht Research

Zachary, LA • On-site

$19.25 - $25.75/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Job Description
Job Description
Why DelRicht Research?

Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you!

Who We Are

DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states.

DelRicht Research has been recognized as a Top Workplace for 2023, 2024, 2025, and 2026!! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.

Limited Term Clinical Research Coordinator's Main Objective

Overall, the Clinical Research Coordinator is responsible for supporting vaccine clinical trials while delivering excellent patient care, maintaining protocol compliance, and flexing into broader site operations as needed:

  • Support clinical research visits across multiple studies in a clinic setting
  • Prepare study medication and coordinate handoff to the blinded team as needed
  • Help create structure and stability during busy or changing visit schedules
  • Follow study protocols, clinic processes, and documentation expectations accurately
  • Communicate clearly with teammates and help the team adapt when priorities shift
  • Maintain professionalism, timeliness, and reliability in a fast-paced clinical environment
Skills needed to win
  • At least 1 year of professional work experience
  • Comfort working in a clinic environment and learning clinical research workflows
  • Strong time management, reliability, and follow-through
  • Tech-savvy and comfortable learning new systems
  • Ability to take direction, stay organized, and support a team through changing priorities
  • A professional, flexible, and team-oriented approach
  • Medical Assistant certification, LPN background, or similar healthcare training
  • Bachelor's degree or equivalent experience, especially for candidates without a clinical certification or licensure
  • Experience supporting patient visits, clinical operations, or healthcare documentation
  • Interest in clinical research, healthcare, or a future medical career
The Right Candidate Will
  • Be self motivated! Energetic! Positive!
  • Bring professionalism, maturity, and strong personal accountability to a fast-paced clinical environment
  • Balance unblinded study responsibilities with the ability to support broader CRC work across general medicine and other site needs
  • Be highly dependable and able to maintain focus in a role that requires precision and trust
  • Be remarkably organized
  • Be skilled at problem solving, planning and being proactive
  • Accept ownership of tasks from inception through completion and assume responsibility for personal success
DelRicht Research's Core Values: Production, Humility, ConsistencyProduction:
  • We deliver on our promises
  • We have a bias towards action: we value independent problem solving
  • We proactively over deliver: we can act without being told what to do and we always have new ideas that will be heard and will improve the company
Humility:
  • We support each other relentlessly
  • We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a can do attitude
  • We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us
  • Coachable: we all love to learn, we are willing to be taught and will adapt quickly
Consistency:
  • We always are able to execute: we get it right the first time and promote touch it once accuracy
  • We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done
  • We are calm under pressure: we can maintain stable performance when under heavy pressure or stress

Job Type: Temporary Full-Time 40+ hrs

Visit our website linked below to learn about our company and current clinical trials, see patient testimonials, and check out our careers page!

Website: www.delrichtresearch.com

Patient Testimonials: https://delrichtresearch.com/testimonials/

We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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