Clinical Study Specialist (Hybrid) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Senior Study Manager Organizes and facilitates the overall planning, coordination, tracking and general performance of clinical studies that support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ensuring clinical study quality and consistency of performance, and
Pursue Progress, Discover Extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesnt happen without people people from different backgrounds, in different locations, doing different roles, all united by one thing: a
Clinical Study Specialist ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at
Senior Clinical Study Manager At Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include applying domain expertise in specific industry segments, utilizing a highly-skilled workforce,
Senior Manager, Global Case Management (Case Management Operations) The Senior Manager, Global Case Management (Case Management Operations), provides day-to-day operational support, subject matter expertise, and oversight of global Individual Case Safety Report (ICSR) management activities. This role supports the effective execution
Description RCCA is seeking a dynamic Regulatory Coordinator Assistant to join our team! This vital role is responsible for handling all regulatory documents and applications essential for launching new clinical trials. As our Regulatory Coordinator Associate,
Systems Engineer - JobID-0209 Department: Engineering Employment Type: Full Time Location: Mount Laurel, NJ Compensation: $90,000 - $184,000 / year Description About The Role: Innovative Defense Technologies (IDT), a leading defense technology company, is seeking a
Job Overview The role of the Staff Accountant resides in the Accounting Department of the Controllers Office. The Controllers Office team is comprised of accounting and finance professionals who are responsible for the general accounting, treasury
Description MikeWorldWide is seeking a well-rounded senior communications professional as Vice President in its New Jersey-based offices. This is a high-growth, high-visibility role for a client service-obsessed leader with experience leading multi-dimensional, multi-workstream accounts. Our ideal
At Zelis, we Get Stuff Done. So, let’s get to it! A Little About Us Zelis is modernizing the healthcare financial experience across payers, providers, and healthcare consumers. We serve more than 750 payers, including the
Benefits: 401(k) Dental insurance Flexible schedule Health insurance Opportunity for advancement Paid time off Training & development Vision insurance Bonus based on performance Are you innovative and revolutionary? Come join the Ellie fam! Clinic Description As
Role Description This is a global role based in the United States. Responsibilities of this role will primarily include the interpretation of digital cytology and hematology cases submitted from markets with Imagyst Digital Cytology service (US and
What Timken makes possible begins with you. Those who came before us helped land a man on the moon, create the worlds infrastructure, and introduce renewable energy alternatives. Now you can join the Timken team to
About Dyania Health Dyania Health exists to make sure no patient misses out on care they need simply because the evidence was buried in their medical records. A persons health story is scattered across years of
The Opportunity: Avantor is looking for a dedicated Research Assistant to optimize our Biopharma / R&D organization. This is a fulltime position based out of our Bridgewater, NJ location. If you have analytical techniques experience –
Clinical Research Coordinator ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
BandLevel 8 Job Description Summary#LI-Hybrid The Global Program Head is a key player in the strategic leadership of Novartis, inspiring action through transformative vision and robust strategies for our programs. They drive the entire program lifecycle,
Job Description: Who We Are We are a dental prosthetics manufacturing organization committed to operational excellence, continuous improvement, and engineering innovation. Our teams bring together expertise in process engineering, quality, production, and maintenance to ensure our
Clinical Research Coordinator – Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward.