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Top Tech Jobs & Startup Jobs in Charlotte, NC
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Feasibility Informatics Manager leads clinical project feasibility, providing strategic input and delivering feasibility studies on time and on budget, collaborating with cross-functional teams to ensure high-quality outcomes.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Site Specialist II role involves supporting regulatory documentation, ensuring compliance for site activation, and collaborating with stakeholders for optimal study performance.
Top Skills:
Microsoft Office Suite
Healthtech • Biotech • Pharmaceutical • Manufacturing
Oversee site contracts for clinical studies, manage contract development, collaborate with teams, ensure financial management, and mentor others.
Top Skills:
Microsoft Office Suite
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance, data integrity, and safety while collaborating with site staff.
Top Skills:
Clinical Trial ProcessesIch-Gcp Guidelines
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Digital Media Buyer develops and implements digital advertising campaigns for patient recruitment, optimizing performance and collaborating on content creation.
Top Skills:
Google Search And Display NetworkMeta ChannelsMicrosoft Office SuiteSpotifyTik TokYoutube
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Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.
Top Skills:
Clinical Trial SoftwareGood Clinical Practice (Gcp) Standards
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Senior CRA / CRA II, you will manage and oversee clinical trial activities, ensuring compliance with protocols, regulations, and industry standards through monitoring and site visits.
Top Skills:
Clinical Trial SoftwareGood Clinical Practice (Gcp) Standards
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Learning & Development Specialist, you will support protocol specific training processes, manage training materials, ensure version control, and contribute to continuous improvement in clinical development.
Top Skills:
Ebis Learning Systems SolutionsLearning Management SystemsMS Office
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Clinical Research Associate at ICON, you will design and analyze clinical trials, ensure protocol compliance, and collaborate with site staff for effective study conduct.
Top Skills:
Ich-Gcp Guidelines
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Clinical Research Associate will conduct site visits, ensure protocol compliance, manage data integrity, and collaborate with site staff in clinical trials.
Top Skills:
Clinical Trial ProcessesIch-Gcp GuidelinesRegulations
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