Clinipace Worldwide, a global digital clinical research organization (dCRO), specializes in serving the drug and medical device development needs of emerging and mid-tier life science firms.
As a dCRO, Clinipace Worldwide has pioneered an innovative service model that has transformed drug and medical device development by delivering technology-amplified services to improve performance, collaboration, and transparency across all stakeholders.
Fueled by TEMPO™ – proprietary eClinical technology – our people ensure your success and execute a shared vision of technology as an enabler to bring both unsurpassed efficiency and quality to your development programs.
With specific expertise in oncology, among other therapeutic areas, Clinipace Worldwide has managed over 500 global contract research and regulatory projects. Clinipace Worldwide is headquartered in Research Triangle Park, North Carolina with offices in Overland Park, Kansas, Boulder, Colorado, Zurich, Switzerland, Munich, Germany, Tel-Aviv, Israel, New Delhi, India, Sao Paulo, Brazil, Buenos Aires, Argentina, and Lima, Peru.
Specialties
contract research organization, CRO, pharmaceuticals, medical devices, regulatory, clinical trials, biotechnology, clinical development, drug development, medical device development
New hires at Clinipace Worldwide
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Associate Director, Regulatory Affairs
Came from...
OPX Biotechnologies, Inc., Associate Director, Analytical Chemistry
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Project Director, Infectious Diseases
Came from...
Camargo Pharmaceutical Services, Sr. Project Manager
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Clinipace Worldwide Activity on LinkedIn
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Clinipace Worldwide has a new Clinical Data Specialist
Amanda Newman is now Clinical Data Specialist, was Senior Test Development Project Manager at Castle Worldwide, Inc.
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Clinipace Worldwide has a new Senior Clinical Research Associate
Annette McGee is now Senior Clinical Research Associate
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Clinipace Worldwide has a new Regulatory Affairs Specialist
Pradnya Bhagwat is now Regulatory Affairs Specialist
