Clinical Research Assistant Jobs in Louisiana
Clinical Research Assistant jobs in Louisiana are steadily active, concentrated in academic medical centers, pharmaceutical research sites, and oncology and infectious disease trial programs, with openings at both entry and experienced levels. The heaviest hiring is in New Orleans, Baton Rouge, and Shreveport, where institutions like Ochsner Health, LSU Health Sciences Center, and Tulane Medical Center consistently bring on clinical research staff. The most in-demand specialties are oncology trials, cardiovascular studies, and community health research tied to Louisiana's chronic disease burden. Find a role that fits below and apply directly.
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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 opportunities 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 in 2023-2026! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.
Team Lead's Main Objective:
DelRicht Research is seeking an experienced Clinical Research Team Lead to guide a team responsible for preparing new clinical trials for successful activation and execution across our growing site network.
This role combines clinical expertise, project management, quality oversight, and people leadership. The Clinical Research Team Lead will help ensure that study resources, internal project plans, and site handoffs are completed accurately and on time. You will work closely with internal site operations, sponsors, Clinical Research Organizations, and DelRicht's centralized departments to identify barriers early, communicate realistic timelines, and position our sites for rapid activation and successful patient enrollment.
The Clinical Research Team Lead is responsible for driving rapid, predictable study activation through strong project management, technical excellence in CRIO, rigorous quality oversight, and proactive collaboration with site operations and centralized departments.
What You'll Do
Lead Study Projects During the Initial Launch of the Trial
- Manage study start-up activities within the team's control, with the goal of positioning DelRicht to achieve first site activated and first site to screen whenever possible.
- Establish, maintain, and communicate accurate activation timelines.
- Maintain detailed project plans reflecting site, study team, and centralized department responsibilities.
- Identify study-specific barriers, dependencies, and trial-limiting factors early.
- Monitor study activation, first patient screening, first patient visits, and first randomization milestones.
Lead and Develop the Team
- Provide day-to-day direction, coaching, and support to assigned coordinators.
- Conduct and document consistent one-on-one meetings.
- Set clear quarterly performance and development goals aligned with department and company priorities.
- Recognize high performers and create opportunities for continued growth.
- Address performance concerns directly, fairly, and promptly.
- Support formal performance reviews and improvement plans when needed.
- Assess team capacity and communicate resource or bandwidth concerns before performance is affected.
- Support hiring, onboarding, and training of new team members.
- Ensure training materials and competency packets are completed accurately and on time.
- Identify opportunities to improve or expand the department's processes and capabilities.
Partner With Sponsors and Clients
- Represent DelRicht professionally in written, verbal, and virtual client interactions.
- Confirm expectations, activation timelines, milestones, and required next steps with sponsors and stakeholders.
- Help facilitate site introductions and early connections between site teams and Clinical Research Associates.
- Provide responsive, service-oriented communication throughout the startup process.
- Escalate concerns internally before they become external issues whenever possible.
- Communicate significant client requests or escalations to the appropriate team members within one business day.
- Ask thoughtful questions and clarify unknowns before making assumptions or moving forward.
Maintain Quality and Compliance
- Ensure all startup resources align with the protocol and client-provided materials.
- Maintain complete, accurate, and audit-ready study documentation.
- Directly review resources before scheduled handoffs and build sufficient review time into project plans.
- Balance urgency with accuracy, compliance, and participant safety.
- Track errors and trends, provide retraining, and implement corrective actions when needed.
- Hold team members accountable for following established processes consistently.
Collaborate Across DelRicht
- Build strong working relationships across al teams at DelRicht.
- Communicate known or suspected protocol concerns to the appropriate team members.
- Identify site, study, and process trends and communicate them proactively.
- Include site teams in decisions that affect their workflows and study execution.
- Provide accurate, timely information that enables other teams to plan effectively.
- Create a positive, solutions-oriented experience in every interaction.
What Success Looks Like
You consistently:
- Deliver milestones within established expectations.
- Position DelRicht sites to activate and begin screening quickly.
- Ensure startup materials are finalized before handoff without delaying first patient visits.
- Maintain accurate project plans and internal trackers.
- Prevent repeat errors and protocol deviations through strong oversight and retraining.
- Retain high-performing team members and address performance concerns promptly.
- Earn positive feedback from site teams, centralized departments, sponsors, and CROs.
- Strengthen DelRicht's reputation for responsiveness, preparation, quality, and execution.
What We're Looking For
Required Qualifications
- At least three years of experience, preferably in a healthcare project management position.
- Bachelor's degree in a healthcare, life sciences, business, or related field.
- Strong understanding of clinical documentation, healthcare operations.
- Experience managing multiple projects and competing deadlines simultaneously.
- Experience coaching, training, or providing day-to-day leadership to other team members.
- Strong written and verbal communication skills.
- Demonstrated ability to identify risks, solve problems independently, and escalate concerns appropriately.
- Exceptional attention to detail and a commitment to getting work right the first time.
- Ability to remain organized and composed in a fast-paced, deadline-driven environment.
The Competencies That Matter Most
- Drives Results: Creates urgency, maintains momentum, and follows through on commitments.
- Plans and Aligns: Develops clear project plans, coordinates dependencies, and prepares teams for upcoming milestones.
- Develops Talent: Provides clear expectations, actionable feedback, and meaningful development opportunities.
- Ensures Accountability: Addresses performance and process concerns directly and promptly.
- Decision Quality: Uses protocol requirements, available information, and sound judgment to make timely decisions.
- Collaborates: Builds trusted relationships across sites, departments, sponsors, and CROs.
- Communicates Effectively: Shares accurate information with the right people at the right time.
- Optimizes Work Processes: Identifies inefficiencies, strengthens workflows, and prevents repeat errors.
- Manages Complexity: Balances multiple studies, stakeholders, priorities, and deadlines without sacrificing quality.
Our Culture
We value people who embody DelRicht Research's core values:
- Production: Delivers results, takes initiative, solves problems independently, and follows through on commitments.
- Humility: Remains coachable, embraces feedback, supports others, and adapts as the organization grows.
- Consistency: Executes accurately, maintains high standards, and remains calm and dependable under pressure.
Team Perks & Benefits at DelRicht Research
- Medical, Dental, and Vision Insurance
- Short-Term and Long-Term Disability Coverage
- Generous Paid Time Off that grows throughout your career with the company
- No nights or weekends
- 401(k) with discretionary match and profit sharing
- Quarterly performance bonus plan with clearly defined goals and earning potential
- Opportunities for professional development and continued career growth
Job Type: Full-Time, 40+ hours per week
Location: Onsite in New Orleans, LA
We are an equal opportunity employer and considers all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
See All 23 Clinical Research Assistant Jobs in Louisiana
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Find JobsClinical Research Assistant Jobs by City in Louisiana
Where Louisiana roles are concentrated, by current openings.
Clinical Research Assistant Job Market in Louisiana
A snapshot from current Louisiana openings, updated as new roles post.
Who's Hiring



Top Industries Hiring
- Education
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What Louisiana Employers Look For
The qualifications that appear most often in clinical research assistant jobs across Louisiana.
- Bachelor's degree in life sciences, biology, or a health-related field required
- Prior experience or coursework in clinical trials or human subjects research preferred
- Familiarity with Good Clinical Practice guidelines and ICH standards expected
- Experience using electronic data capture systems such as REDCap or Medidata
- Strong attention to detail for accurate regulatory documentation and case report forms
- Ability to obtain CITI Program certification in human subjects research protection
Clinical Research Assistant Jobs in Louisiana: Frequently Asked Questions
How do you become a clinical research assistant in Louisiana?
Most Louisiana employers require a bachelor's degree in a life science, nursing, or public health field as the baseline entry point. Louisiana does not issue a state license specific to clinical research assistants, but employers expect completion of CITI Program training in human subjects research protection before or shortly after hire. Candidates who pursue the Society of Clinical Research Associates certification gain a measurable edge at institutions like LSU Health and Ochsner Health.
Which companies hire clinical research assistants in Louisiana?
Louisiana clinical research assistant roles are posted by Ochsner Health, Tulane University, and FMOL Health and others right now, based on current listings on Migrate Mate as of September 2026. Louisiana's concentration of academic medical centers and federally funded research programs means hospital systems and university health sciences campuses make up the largest share of consistent openings in the state.
Which Louisiana cities have the most clinical research assistant jobs?
New Orleans, Shreveport, and Baton Rouge account for the most clinical research assistant openings in Louisiana. New Orleans leads because of its density of academic medical centers and research hospitals, while Baton Rouge benefits from the LSU Health Sciences Center campus and pharmaceutical industry activity, and Shreveport draws openings through LSU Health Shreveport and its associated clinical trial programs.
Are there remote clinical research assistant jobs in Louisiana?
Yes, but they're rare. Clinical research assistant work is largely site-based, involving direct patient contact, regulatory binder management, and on-site monitoring that cannot be done remotely. About 33% of clinical research assistant openings tied to Louisiana are remote or hybrid as of September 2026, and those positions tend to cover data entry, protocol review, or sponsor-facing coordination tasks rather than active trial support.
How can I get hired as a clinical research assistant in Louisiana with little or no experience?
The most realistic entry path is applying to research coordinator trainee or clinical research associate I roles at Louisiana's large academic health systems, particularly Ochsner Health, Tulane Medical Center, and LSU Health New Orleans, which regularly onboard candidates from their affiliated undergraduate and nursing programs. Lateral moves from roles like medical assistant, phlebotomist, or clinical data entry specialist are common stepping stones. Completing CITI Program certification before applying and volunteering through university IRB-approved student research programs strengthens any application significantly.
Where can I find and apply to clinical research assistant jobs in Louisiana?
You can find and apply to clinical research assistant jobs in Louisiana on Migrate Mate, which lists current Louisiana openings across hospitals, research institutions, and trial sites. Find the roles that fit your background and apply directly to the ones that match.
See All 23 Clinical Research Assistant Jobs in Louisiana
Find roles in Louisiana that match your experience and apply in just a few clicks.
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