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Senior Regulatory Affairs Associate

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Join Parexel Consulting as a Senior Regulatory Affairs Associate in India. Utilize your expertise in Biologicals, Vaccines, and small/large molecules to develop global regulatory strategies for US, EU, and other key markets. You will prepare and review Marketing Authorization Applications, enjoyi...
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India
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Not provided
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Until further notice

Regulatory Affairs Generalist

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Join Parexel Consulting as a Regulatory Affairs Generalist. Use your scientific degree and industry experience to develop strategies for biopharma and medical device clients. Manage submissions, lifecycle maintenance, and health authority interactions in a flexible, supportive global environment.
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Regulatory Affairs Generalist

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Join Parexel Consulting as a Regulatory Affairs Generalist in the UK. Use your scientific degree and regulatory experience to help biopharmaceutical clients navigate complex requirements. You will manage submissions, lifecycle maintenance, and health authority interactions. Enjoy flexible work, c...
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United Kingdom
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Not provided
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Senior Clinical Research Associate

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Join Parexel as a Senior Clinical Research Associate (CRA) in the Paris Region. You will ensure data integrity and ICH-GCP compliance at investigator sites, working on global projects across diverse therapeutic areas. We seek a professional with a relevant degree, excellent communication skills, ...
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France , Paris Region
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Regulatory CMC Project Manager

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Join Parexel as a Regulatory CMC Project Manager. Utilize your 3+ years of CMC regulatory experience to manage complex submissions and strategic plans for biopharma clients. Enjoy a fully remote role with East Coast hours, career growth, and expert mentorship. Be part of a supportive team shaping...
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United States
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Clinical Research Associate

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Join Parexel in Taiwan as a Clinical Research Associate (CRA). You will ensure patient safety and protocol adherence at investigator sites, managing global projects across diverse therapeutic areas. The role requires fluency in Japanese and Mandarin, plus strong site management skills. We offer f...
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Taiwan
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Research Associate

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Join Parexel's Early Phase Clinical Unit in Glendale, CA, as a Research Associate. You will play a crucial role in Phase I trials, conducting participant visits and ensuring protocol compliance. This role requires a Certified Phlebotomy Technician I license and clinical/patient experience. We off...
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Location
United States , Glendale
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Salary
20.00 - 26.00 USD / Hour
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Scientist III - Third Shift - Analytical Chemist Pilot Plant

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Join our team as a Scientist III - Analytical Chemist on the third shift in Rahway, NJ. This role requires hands-on experience with HPLC, GC, and wet chemistry methods within a cGMP environment. You will operate and maintain analytical instrumentation, ensuring high-quality, compliant results. We...
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United States , Rahway, New Jersey
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Senior Integration Engineer

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Seeking a Senior Integration Engineer in India with 7+ years of software engineering experience. This role requires deep expertise in MuleSoft 4, API-led connectivity, and designing SOAP/REST services. You will develop high-quality integrations, follow DevOps practices, and collaborate with globa...
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India
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Veeva Clinical Digital Systems Analyst

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Join Parexel as a Veeva Clinical Digital Systems Analyst in Poland. You will optimize clinical trial processes by managing digital systems, bridging technology and operations. This role requires 5+ years in clinical technology and offers a performance bonus, career development, and a friendly wor...
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Poland
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Salary
260000.00 - 351000.00 PLN / Year
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Health Economics Consultant

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Join Parexel Consulting as a Health Economics Consultant in the UK. Utilize your advanced degree and 3+ years of industry experience in health economics and statistics. You will design evidence-generation strategies and conduct analyses using R/GitLab to support market access. Enjoy flexible work...
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United Kingdom
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Not provided
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Senior Clinical Research Associate

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Join Parexel as a Senior Clinical Research Associate (CRA) in the UK. You will ensure protocol and ICH-GCP compliance, with recent oncology experience being essential. This role offers flexible work arrangements, career development, and exposure to diverse global therapeutic projects. Build key r...
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United Kingdom
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Not provided
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