Scientist Jobs in Louisiana
Scientist jobs in Louisiana are concentrated in Baton Rouge, New Orleans, and Lafayette, where employers like ExxonMobil, the LSU Health Sciences Center, and the Pennington Biomedical Research Center maintain a consistent and lasting presence. The most in-demand specialties include environmental science, petrochemical research, and biomedical research, reflecting the state's deep ties to the energy sector and its growing life sciences infrastructure. Openings range from entry-level research associate positions to senior principal scientist roles. Scan the live roles below and apply to whichever ones fit.
Find Scientist JobsOverview
Showing 5 of 22+ Scientist jobs
Updated: Yesterday
Location: Remote, LA, United States
Job ID: 25112668-OTHLOC-1500-2DLA-2DR
Join our Talent Network
Description
Clinical/Medical Scientist (Medical Monitoring) - Oncology - BreastOur Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
- Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans.
- Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro-actively identifies and resolves medical data review issues as they arise.
- Authors medical data queries and reviews query responses, approves query closure in association with Medical Director.
- May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed.
- Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed.
- Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review.
- Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner.
- Attends and present at Trusted Process meetings and may participate in internal and external audits.
- Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology.
- Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans.
- May manage limited number of direct reports. May participate or conduct interviews.
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$67,700.00 - $115,100.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Partners with medical director and other team members on clinical and scientific input for phase I-IV clinical trials with an emphasis on protocol-specific requirements and ensuring the scientific integrity and data quality of clinical trials by using scientific knowledge. Collaborates with Medical Director(s) and other team members on data reviews, and other Medical Management activities to ensure the successful execution and conduct of clinical trials.Updated: Yesterday
Location: Remote, LA, United States
Job ID: 25112668-OTHLOC-1500-2DLA-2DR
Join our Talent Network
Description
Clinical/Medical Scientist (Medical Monitoring) - Oncology - BreastOur Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
- Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans.
- Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro-actively identifies and resolves medical data review issues as they arise.
- Authors medical data queries and reviews query responses, approves query closure in association with Medical Director.
- May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed.
- Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed.
- Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review.
- Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner.
- Attends and present at Trusted Process meetings and may participate in internal and external audits.
- Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology.
- Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans.
- May manage limited number of direct reports. May participate or conduct interviews.
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$67,700.00 - $115,100.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Partners with medical director and other team members on clinical and scientific input for phase I-IV clinical trials with an emphasis on protocol-specific requirements and ensuring the scientific integrity and data quality of clinical trials by using scientific knowledge. Collaborates with Medical Director(s) and other team members on data reviews, and other Medical Management activities to ensure the successful execution and conduct of clinical trials.See All 22 Scientist Jobs in Louisiana
Find roles in Louisiana that match your experience and apply in just a few clicks.
Find Scientist JobsScientist Jobs by City in Louisiana
Where Louisiana roles are concentrated, by current openings.
Scientist Job Market in Louisiana
A snapshot from current Louisiana openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Education
What Louisiana Employers Look For
The qualifications that appear most often in scientist jobs across Louisiana.
- Bachelor's degree in a scientific discipline recognized by the hiring institution in Louisiana
- Experience with environmental monitoring, chemical analysis, or laboratory research methods
- Proficiency with scientific instrumentation and data analysis software such as LIMS or R
- Familiarity with Louisiana DEQ or federal EPA compliance protocols for regulated industries
- Ability to document research findings and prepare technical reports for internal and external audiences
- Strong collaboration skills for cross-functional teams in petrochemical, biomedical, or academic settings
Scientist Jobs in Louisiana: Frequently Asked Questions
How do you become a scientist in Louisiana?
Most scientist roles in Louisiana require at minimum a bachelor's degree in biology, chemistry, environmental science, or a related field, with many research and senior positions requiring a master's or doctoral degree. Louisiana does not require a state-issued license for the general scientist title, but environmental scientists working with regulated pollutants may need certifications recognized by the Louisiana Department of Environmental Quality. Building experience through university research programs at LSU, Tulane, or UNO strengthens a candidate's profile considerably.
Which companies hire scientists in Louisiana?
Louisiana scientist roles are posted by CHRISTUS Health, LCMC Health, and LSU Health Sciences Center - New Orleans and others right now, based on current listings on Migrate Mate as of September 2026. Louisiana's energy corridor along the Mississippi River and its expanding biomedical research institutions mean demand comes from both industrial and academic employer types.
Which Louisiana cities have the most scientist jobs?
New Orleans, Metairie, and Louisiana have the most scientist openings in Louisiana. Baton Rouge leads because of its dense concentration of petrochemical facilities along the industrial corridor and the presence of LSU's flagship research campus, while New Orleans draws biomedical and environmental scientists through its major hospital systems, coastal research centers, and universities including Tulane and Xavier.
Are there remote scientist jobs in Louisiana?
Yes, but they're rare. Scientist work in Louisiana is heavily lab-based, field-based, or tied to industrial facilities, which limits the share of fully remote positions. About 29% of scientist openings tied to Louisiana are remote or hybrid as of September 2026, and those that are tend to involve data analysis, regulatory review, or technical writing rather than hands-on research.
How can I get hired as a scientist in Louisiana with little or no experience?
The most realistic entry path is applying for research associate or laboratory technician roles at Louisiana universities or large industrial employers, which regularly bring on candidates with a bachelor's degree and internship experience. LSU, Tulane, and the Pennington Biomedical Research Center all run undergraduate and early-career research programs that serve as direct pipelines into full-time positions. Lateral moves from quality control technician or environmental field sampler roles are also common entry points into scientific careers in Louisiana.
Where can I find and apply to scientist jobs in Louisiana?
You can find and apply to scientist jobs in Louisiana on Migrate Mate, which lists current Louisiana openings. Search the available roles, find the ones that match your background and location, and apply directly to the ones that fit.
See All 22 Scientist Jobs in Louisiana
Find roles in Louisiana that match your experience and apply in just a few clicks.
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