ZipRecruiter

Log In

2

Entry Level Biotech Clinical Research Jobs in Raleigh, NC

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

We assist clinical research throughout the lifecycle of development, from drug concept to ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?

INC Research

Biometrics Project Manager

Raleigh, NC

Company Description INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and ...

INC Research

Biometrics Project Manager

Raleigh, NC · On-site

Company Description INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and ...

Ergomed

Clinical Team Manager

Raleigh, NC · On-site

Ergomed is a specialist clinical research organization focused on rare disease and select oncology ... We partner with small to midsize biotech companies to move promising therapies through early phase ...

INC Research

Senior Biostatistician

Raleigh, NC · On-site

Company Description INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and ...

INC Research

Senior Biostatistician

Raleigh, NC · On-site

Company Description INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and ...

MMS

Nonclinical Writer

Raleigh, NC · On-site

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ...

Revival Research Institute, LLC

Phlebotomist/Lab Tech

Cary, NC · On-site

$15.75 - $19.75/hr

Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not ...

IQVIA

CRA 2/Senior CRA

Durham, NC · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

IQVIA, Inc.

CRA 2/Senior CRA

Durham, NC · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

IQVIA

CRA 2/Senior CRA

Durham, NC · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

previous pagenext page

Showing results 21-40

All JobsBiotech Clinical Research JobsEntry Level Biotech Clinical Research JobsEntry Level Biotech Clinical Research Jobs in Raleigh, NC

Entry Level Biotech Clinical Research information

See Raleigh, NC salary details

$12

$23

$39

How much do entry level biotech clinical research jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for entry level biotech clinical research in Raleigh, NC is $23.42, according to ZipRecruiter salary data. Most workers in this role earn between $19.62 and $24.09 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Biotech Clinical Research vs Entry Level Pharmaceutical Sales Representative?

AspectEntry Level Biotech Clinical ResearchEntry Level Pharmaceutical Sales Representative
Required CredentialsBachelor's in life sciences, certification preferredBachelor's degree, sales or marketing background beneficial
Work EnvironmentLaboratory, clinical trial sites, officeMedical offices, hospitals, client meetings
Industry UsageResearch institutions, biotech companiesPharmaceutical companies, healthcare providers
Common Search/ComparisonYesNo

Entry Level Biotech Clinical Research involves supporting clinical trials, data collection, and regulatory compliance within research settings. In contrast, Entry Level Pharmaceutical Sales Representatives focus on promoting products to healthcare professionals and building client relationships. Both roles require a bachelor's degree, but their work environments and industry functions differ significantly.

What are popular job titles related to Entry Level Biotech Clinical Research jobs in Raleigh, NC? For Entry Level Biotech Clinical Research jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Entry Level Biotech Clinical Research jobs in Raleigh, NC look for? The top searched job categories for Entry Level Biotech Clinical Research jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Entry Level Biotech Clinical Research jobs? Cities near Raleigh, NC with the most Entry Level Biotech Clinical Research job openings:
Entry Level Biotech Clinical Research jobs near you
Infographic showing various Entry Level Biotech Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $48,709 per year, or $23.4 per hour.

Clinical Project Coordinator

CTI

Raleigh, NC • On-site

Full-time

Medical, PTO

Re-posted 19 days ago

Job description

Job Summary: The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. **Please note that this position is office based to be filled at our Covington, KY or Raleigh, NC office location.**
What You'll Do
  • Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required deliverable as appropriate
  • Update Clinical Project Manager / Director on progress, outstanding items, and issues as they arise; support Clinical Project Manager / Director with issue resolution
  • Assist Clinical Project Manager / Director or Clinical Research Manager / Clinical Operations Director with preparing data reports for site and Clinical Research Associate (CRA) management; provide support for site management activities
  • Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in reviewing and maintaining these presentations and documents as required per CTI Standard Operating Procedures (SOPs)
  • Prepare initial drafts, including templates and content, of internal reports, external reports, newsletters, and other clinical project communications; distribute reports and communications to sites, vendors, Sponsors, and internal team members
  • Assist with tracking project scope and internal financial reporting
  • Prepare initial drafts of detailed meeting agendas and minutes; assist in initial review of meeting documents prepared by others; attend routine internal and external team meetings
  • Monitor and maintain tracking tools, clinical systems and shared document repositories utilized for clinical project management
  • Manage and maintain CTI clinical system user account requests
  • Support the review and tracking of site prescreening, screening, and enrollment activities as well as subject status information; follow up with internal clinical project team and/or sites as necessary regarding any identified issues
  • Support tracking of action items and internal team follow-up
  • Support and prepare / maintain tracking of clinical project start-up activities and milestones, including site selection and site start-up activities
  • Assist the clinical project team and/or the Feasibility Department with developing feasibility surveys and survey content; participate in feasibility calls; assist with any site follow-up needed throughout start-up
  • Assist clinical project team with tracking and filing of clinical project plan and/or Standard Operating Procedure (SOP)-related deviations
  • Support and maintain clinical project documents in paper and/or electronic Trial Master Files and support Clinical Project Manager / Director with TMF reconciliation and period review follow-up
  • Create and compile the Investigator Site File and Pharmacy Binde or Study Manual in collaboration with CPM/RASSU/Clinical Monitoring. Organize shipments to CRA/Site. Includes set-up and maintenance of Index with Comments.
  • Participate in preparing and following-up from internal and external audits; participate in audits as needed
  • Assist with the management of all clinical project-related supplies and drug management
  • Assist other departments as needed throughout all phases of clinical projects (e.g., Regulatory Affairs Study Start-up, Data Management, Safety, etc.)
  • Provide support in developing new Clinical Project Coordinators, Clinical Project Assistants, and Research Associates (RAs) in clinical projects
  • Assist with orientating new Clinical staff
  • Provide third party vendor support
  • Represent CTI in professional manner and foster collaboration with all clinical project teams / functional departments; assist in promoting interdepartmental cohesiveness

What You'll Bring
  • Bachelor's degree in allied health fields such as nursing, pharmacy, or health / natural science or an equivalent combination of education and relevant work experience
  • At least 1 year of experience in clinical research related field

About CTI
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
Why CTI?
  • Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
  • Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
  • Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important NoteIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Veterans/Disabled
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

Apply