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Clinical Research Jobs in Baton Rouge, LA (NOW HIRING)

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 information

See Baton Rouge, LA salary details

$47.1K

$103.1K

$181.5K

How much do clinical research jobs pay per year?

As of Aug 22, 2026, the average yearly pay for clinical research in Baton Rouge, LA is $103,068.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,800.00 and $117,600.00 per year, depending on experience, location, and employer.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

What is the difference between Clinical Research vs Clinical Data Coordinator?

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
More about Clinical Research jobs

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The most popular types of Clinical Research jobs in Baton Rouge, LA are:

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What cities near Baton Rouge, LA are hiring for Clinical Research jobs?

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Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 95% Full Time, and 5% Part Time. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $103,068 per year, or $49.6 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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