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Entry Level Clinical Operations Jobs in Raleigh, NC

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Entry Level Clinical Operations information

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$34K

$95.3K

$181.3K

How much do entry level clinical operations jobs pay per year?

As of Aug 17, 2026, the average yearly pay for entry level clinical operations in Raleigh, NC is $95,302.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in entry level clinical operations?

To thrive in an Entry Level Clinical Operations role, you generally need a bachelor's degree in a life science or health-related field, strong organizational skills, and a keen attention to detail. Familiarity with clinical trial management systems (CTMS), Microsoft Office Suite, and Good Clinical Practice (GCP) guidelines is often expected. Strong communication, problem-solving abilities, and the capacity to work both independently and collaboratively will help you stand out. These skills and qualities are crucial for ensuring the smooth execution of clinical studies, maintaining regulatory compliance, and supporting cross-functional project teams.

What are the typical responsibilities in an entry level clinical operations role?

In an Entry Level Clinical Operations position, your daily tasks may include supporting clinical trial documentation, coordinating communication between sites and sponsors, assisting with regulatory submissions, and tracking study milestones. You may also help oversee study timelines, maintain trial master files, and participate in team meetings to ensure project progress. The role often involves working closely with clinical research associates, project managers, and data management teams. This hands-on experience offers valuable insight into the clinical research process and can serve as a strong foundation for advancing your career in clinical operations.

What is an entry level clinical operations?

An Entry Level Clinical Operations job involves supporting the planning, execution, and management of clinical trials to ensure they run smoothly and comply with regulatory guidelines. Responsibilities may include coordinating trial logistics, maintaining documentation, assisting with site communications, and ensuring adherence to protocols. This role provides exposure to various aspects of clinical research and serves as a stepping stone for growth in clinical project management or regulatory affairs. Strong organizational skills, attention to detail, and knowledge of Good Clinical Practice (GCP) are essential for success in this role.

What are the most commonly searched types of Clinical Operations jobs in Raleigh, NC?

The most popular types of Clinical Operations jobs in Raleigh, NC are:

What are popular job titles related to Entry Level Clinical Operations jobs in Raleigh, NC?

For Entry Level Clinical Operations jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Operations jobs in Raleigh, NC look for?

The top searched job categories for Entry Level Clinical Operations jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Entry Level Clinical Operations jobs?

Cities near Raleigh, NC with the most Entry Level Clinical Operations job openings:

Entry Level Clinical Operations jobs near you
Infographic showing various Entry Level Clinical Operations job openings in Raleigh, NC as of July 2026, with employment types broken down into 69% Full Time, 24% Part Time, and 7% Temporary. Highlights an 100% In-person job distribution, with an average salary of $95,302 per year, or $45.8 per hour.

Development Technologist or Research Technician, Rotational Program

Locus Biosciences, Inc.

Morrisville, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our company in a full-time, entry-level position that will rotate between our Chemistry, Manufacturing and Controls (CMC) and Research & Development (R&D) departments during this 2 year rotational program. This position is well suited for those looking for an entry-level position that is excited to learn all aspects of biotechnology drug development from early-stage research through drug product manufacturing. Candidates will be expected to accomplish defined work, as well as assist in approaching and solving complex scientific problems. Candidates should have demonstrated laboratory or manufacturing experience, with solid communication, technical aptitude, and problem-solving skills. Experience working in regulated, pharmaceutical/biotechnology R&D (GDP, GLP) and/or manufacturing environments (cGMP) is strongly preferred, but not required.
Why Locus?
  • Change the future of medicine and address a serious and unmet patient need by developing completely novel therapeutic modalities.
  • Fast-track your career by tackling large & meaningful projects and learning a breadth of techniques and skillsets in the wet lab and manufacturing suites
  • Work with a team of exceptionally talented and hardworking individuals while striving to achieve a common mission
  • Partner with the most highly respected pharmaceutical companies in the world
  • Bonus pool eligibility
  • Health, dental, vision, life insurance, 401(k), and PTO
  • Free access to fitness center and classes

Responsibilities will include:
  • Designing and/or executing formulation development activities
  • Designing and/or executing bench-scale process development activities, including set-up and operation of development-scale bioreactors, filter trains, tangential flow filtration (TFF) equipment, and chromatography equipment
  • Development of analytical strategies to inform formulation and process development activities
  • Design and deploy automated workflows for molecular biology and microbiology assays, including liquid handling automation, next-generation sequencing (NGS) library preparation, and high-throughput screening of phage activity to accelerate research timelines and improve experimental reproducibility.
  • Support the development of data infrastructure and bioinformatics pipeline for R&D and CMC operations, including DNA sequence analysis, sequence assembly, and comparative genomic analysis.
  • Molecular biology and synthetic biology- Cloning, NGS library preparation, characterization of novel genetic engineering tools, and generation and analysis of novel engineered phage clones
  • Microbiology - Culturing both aerobic and obligate anaerobic organisms. Utilizing a range of bacterial strains to produce and characterize activity of phage
  • Independent management, planning, and execution of multiple projects, including reviewing, interpreting, and recording results.
  • Supporting tech transfer of new products and processes to ensure smooth transition from R&D to process development to GMP manufacturing
  • Forming strong relationships with all stakeholders, including technicians, associates, project and program managers, and scientists to enable successful tech transfer
  • Supporting Scientists in all aspects of pharmaceutical development
  • Assisting in the preparation of batch records, protocols, SOPs, deviations, technical reports, presentations, and other CMC documents to support drug development, including INDs, BLAs, and other applications
  • Gaining aseptic gowning and fill qualification
  • Performing material handling and staging
  • Practicing real-time documentation (such as batch records) during production run and maintain accurate records/logs according to GDP
  • Supporting Qualification and Validation activities
  • Identifying, communicating, and troubleshooting process issues
  • Supporting team effort in the effective and timely completion of root cause investigations and CAPA
  • Supporting a high-performance teamwork environment

Rotations may include a combination of any of the following functions:
  • Research and Development including but not limited to phage discovery, phage engineering, and strain engineering.
  • High Throughput Development (Automation)
  • Bioinformatics
  • Material Sciences & Technology
  • cGMP Manufacturing
  • Analytical Development
  • Quality Control
  • Clinical Lab
  • Quality Assurance
  • Project Management Office
  • Clinical Operations

Education:
  • Technical certificate or degree (e.g. BTEC Biomanufacturing), or graduation from an accredited college/university with a Bachelor's to a Master's degree in Biology, Chemistry, Biochemistry, Chemical Engineering, Biophysics, Pharmaceutical Technology or related field, with some lab experience (required)

Experience and Expertise:
  • Familiarity with general laboratory techniques such as pipetting, serial dilutions, aseptic technique and proper decontamination procedures
  • Experience in research, pharmaceutical, biotechnology, and/or sterile production environment
  • Experience executing SOPs and documenting work
  • Strong mechanical aptitude
  • Excellent oral and written communication skills
  • Technical writing ability
  • Thrives in a fast-paced, entrepreneurial and collaborative environment. Openly shares knowledge/information needed to accomplish a task or solve a problem

Preferred Qualifications:
  • At least two years' experience between academic or industry research
  • Experience in biologics (upstream, downstream, aseptic fill/finish) with working knowledge of FDA regulations and GMP systems
  • Experience with DNA sequence analysis, including homology searching, sequence assembly and primer design
  • Ability to assist in the design of experiments and interpretation of results
  • Motivation to learn new processes that contribute to the company's overall desire to get products into the clinic
  • Technical proficiency with designing and executing standard molecular biology experiments (PCR, transformation, Gibson cloning)
  • Experience with microbiology skills like growth curves, anaerobic microbiology, streaking and banking strains

*The level of the position will be based on the successful candidate's qualifications.
About Locus Biosciences
Locus Biosciences is a clinical-stage biotechnology company developing precision antibacterial products to address critical unmet medical needs in treating bacterial infections and microbiome indications. The Locus platform engineers bacterial viruses called bacteriophages to specifically kill target pathogens while leaving non-target bacteria (i.e., the rest of the patient's microbiome) unharmed and to deliver biotherapeutic payloads to the body sites where they are needed. Locus's lead program is an engineered bacteriophage product targeting Escherichia coli bacteria in the urinary tract, currently being tested in an active Phase 2/3 clinical trial. Locus has collaborations with BARDA and CARB-X to develop engineered bacteriophage products targeting E. coli infections and Klebsiella pneumoniae infections, respectively. For more information about Locus visit https://www.locus-bio.com/
SHIFT: Full-Time Days, with occasional evening and weekend work
Job Type: Full-time, onsite
Job Location: Research Triangle Park, North Carolina
Direct applicants only. No agencies please.

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