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Associate Safety Specialist, Clinical Data Associate I

Thermo Fisher Scientific

0–2 years for Associate Safety Specialist; at least 2 - 4 years for CDA I

October 16, 2026

Online Application

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CDM Programmer I

Thermo Fisher Scientific

0 - 2 Years

October 16, 2026

Online Application

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Scientist Pharmacometrics Support

Johnson & Johnson

1–3 years

October 16, 2026

Walk In Interview

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Clinical Data Programmer SAS II

Novotech

2 Years+

October 16, 2026

Online Application

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Clinical Trial Support Specialist

Bristol Myers Squibb

2 - 4 Years

October 16, 2026

Online Application

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Pharmaceutical Analyst and Clinical Data Specialist

IQVIA

1 - 6 Years

October 16, 2026

Online Application

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Research Associate and Biobanking Quality & Operations Consultant

IAVI

2 - 4 Tears

October 16, 2026

Online Application

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Associate Functional Programmer

Novo Nordisk

1–2 years of experience in clinical data management systems, bioinformatics, or as a Clinical Research Associate.

October 16, 2026

Online Application

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Clinical Resourcing Specialist

Syneos Health

1–3 years

October 15, 2026

Online Application

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Medical Writing, Clinical Trial Management and Site Payments

Thermo Fisher Scientific

3 - 10 Years

October 15, 2026

Online Application

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Associate Safety Specialist, Clinical Data Associate I

CDM Programmer I

Scientist Pharmacometrics Support

Clinical Data Programmer SAS II

Clinical Trial Support Specialist

Pharmaceutical Analyst and Clinical Data Specialist

Research Associate and Biobanking Quality & Operations Consultant

Associate Functional Programmer

Clinical Resourcing Specialist

Medical Writing, Clinical Trial Management and Site Payments

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