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Contract Biologic Coordinator Jobs in Raleigh, NC

... Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development ... Manage project design development through scope definition, design coordination, constructability ...

Primary responsibilities: ● Responsible for assessment and coordination of medical care related ... Evaluate return to work concerns from a physical capability and biological risk to human or product ...

Registered Nurse

Clayton, NC · On-site

$55 - $69/hr

Responsible for assessment and coordination of medical care related to worker's compensation ... Evaluate return to work concerns from a physical capability and biological risk to human or product ...

New

Contract-to-Hire Opportunity ❤️ As a Patient Access Specialist, you'll play a critical role in ... Medical Office Coordinator ???? Healthcare Customer Service Representative ???? Insurance ...

Maintain effective communication, coordination, and working relations with other personnel and ... Conceive of and develop new research areas/products/contract services. * Additional ...

Maintain effective communication, coordination, and working relations with other personnel and ... Conceive of and develop new research areas/products/contract services. * Additional ...

Showing results 41-60

Contract Biologic Coordinator information

See Raleigh, NC salary details

$16

$27

$41

How much do contract biologic coordinator jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for contract biologic coordinator in Raleigh, NC is $27.52, according to ZipRecruiter salary data. Most workers in this role earn between $21.49 and $31.78 per hour, depending on experience, location, and employer.

What is the difference between Contract Biologic Coordinator vs Contract Clinical Research Associate?

AspectContract Biologic CoordinatorContract Clinical Research Associate
Required credentialsBachelor's in life sciences, relevant certificationsBachelor's in life sciences, relevant certifications
Work environmentLaboratories, biotech companies, clinical trial sitesClinical trial sites, pharmaceutical companies, CROs
Employer and industry usageBiotech and pharmaceutical companies focusing on biologicsPharmaceutical companies, CROs conducting clinical trials

Both roles often require similar educational backgrounds and certifications, working within clinical or laboratory settings. The Contract Biologic Coordinator primarily manages biologic product processes, while the Contract Clinical Research Associate oversees clinical trial activities. They share industry environments but focus on different aspects of the drug development process.

Infographic showing various Contract Biologic Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $57,238 per year, or $27.5 per hour.

Full-time

Re-posted 8 hours ago


Key responsibilities

  • Assist with contractual and financial execution of projects, including proposals, change orders, revenue recognition, and monthly budget review.

  • Analyze complex business problems using data to provide insights, identify trends, and develop forecasts and strategic plans.

  • Support business development activities such as forecasting, capacity planning, program onboarding, and tracking scopes of work.


KBI Biopharma rating

6.3

Company rating: 6.3 out of 10

Based on 7 frontline employees who took The Breakroom Quiz


Job description

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.

Position Summary:

Join a highly technical analytical team in a dynamic work environment as a member of the Analytical, Formulation and Stability (AFS) department and participate in contracted client analytical programs for monoclonal antibodies, recombinant proteins, and peptides as a Business Intelligence Analyst. The Business Intelligence Analyst will provide support to their department and/or the Global CAPS organization by conducting data analysis as it relates to financial performance, metric tracking, capacity modelling, financial forecasting, adherence to budget and portfolio analyses. Role will work closely with departmental leadership in preparation of annual budget and mid-term plan and coordinate with other departments as needed (i.e. Finance, PMO, Business Development).

Position Responsibilities:

  • Assists with contractual and financial execution of projects, including proposals, change orders, revenue recognition, and monthly budget review. Includes review of costs and identifying errors and/or misallocations for spend and working with finance to resolve and support of CapEx forecasting and management.
  • Support business development new business forecasting, capacity planning, program on-boarding, and deliverable delivery. May support drafting or review of proposals and change orders and/or tracking and monitoring of scopes of work.
  • Analyzes complex business problems and issues using data from internal and external sources to provide insight to decision-makers. Identifies and interprets trends and patterns in datasets to locate influences. Constructs forecasts, recommendations and strategic/tactical plans based on business data and market knowledge. Creates specifications for reports and analysis based on business needs and required or available data elements. May provide consultation to users and lead cross-functional teams to address business issues. May directly produce datasets and reports for analysis using system reporting tools.
  • Special cross-group/functional projects
  • Champions, maintains, and publishes key departmental performance metrics
  • Assists development of annual budget and MTP
  • Able to react to change productively and handle other essential tasks as assigned.

Position Requirements:

  • Minimum requirement BS/BA degree and 3-5 years of experience; MBA and/or PMP preferred.
  • Interpersonal soft skills and ability to work well with a diverse group of contributors.
  • Business acumen & long-term planning viewpoint, ability to problem solve and set priorities.
  • Demonstrated experience in project management, coordination of cross-functional teams.
  • High integrity and personal responsibility, action oriented.
  • Excellent written & oral communication and presentation skills.
  • Knowledge of biologics industry is preferred but not required.

About KBI:

KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com.

KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.


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