CRA II: Lead Global Clinical Trials ( )
Everest Clinical Research
Everest Clinical Research is hiring a Clinical Research Associate II in Bridgewater, NJ. The successful candidate will monitor clinical trials, ensuring compliance with ICH-GCP guidelines and facilitate communication between sponsors and investigational sites. The role demands a Bachelor's in Life Science, 4+ years of relevant experience, and strong organizational skills. Travel of up to 70% is required for this position. #J-18808-Ljbffr
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the CRA II: Lead Global Clinical Trials ( ) in Bridgewater, NJ vacancy
$199k - $343k
...Function: Discovery & Pre-Clinical/Clinical Development Job Sub... ...finding treatments and cures. We lead where medicine is going and... ...Approval Access (PAA) programs globally, serving as the primary Study... ...Medical Affairs (GMAF) clinical trials, ensuring scientific integrity...SuggestedTemporary workLocal areaRemote work- ...Rutgers University in New Jersey is seeking a Clinical Research Coordinator II to manage tuberculosis research studies. The role involves overseeing multiple clinical protocols with responsibilities including patient recruitment, data management, compliance with regulatory...Suggested
- ...Legend Biotech, located in Raritan, NJ, is hiring a Global Viral Vector MSAT Lead to provide technical leadership in viral vector manufacturing. The role emphasizes ensuring compliance and scalability in processes and includes mentoring a team of scientists. Key responsibilities...SuggestedFull timeFor contractors
- Legend Biotech is a global biotechnology company dedicated to treating, and one day curing... ...myeloma. Global Viral Vector MSAT Lead as part of the Global Manufacturing & Supply... ...manufacturing supporting in vivo programs across clinical development and commercial lifecycle...SuggestedPermanent employmentFull timeFor contractorsLocal areaWorldwide
- Legend Biotech US is seeking a Global Viral Vector MSAT Lead to provide oversight in viral vector manufacturing for in vivo programs. The responsible... ...closely with cross-functional teams to secure reliable clinical supply. This role requires a minimum of 10 years of MSAT...Suggested
- Legend Biotech is seeking a Global Viral Vector MSAT Lead based in Raritan, NJ. The role requires technical leadership in viral vector manufacturing, ensuring robust processes for compliance and scalability. Ideal candidates will possess a B.S. degree and at least 10 years...
- 360-IT-Professional is seeking a Web Lead to be a key contributor to the Web & Mobile Services team. The candidate will work on global Web Development using WebSphere and Hybris platforms, contributing significantly to e-commerce initiatives. The ideal candidate should...
- Legend Biotech seeks a Global Viral Vector MSAT Lead in Raritan, NJ, to provide technical leadership for viral vector manufacturing. The ideal candidate will have a robust knowledge of MSAT processes and over 10 years of relevant experience. Your key responsibilities include...Full time
- Legend Biotech is seeking a Global Viral Vector MSAT Lead in Raritan, NJ. In this role, you will provide technical leadership for viral vector manufacturing processes, ensuring compliance and scalability. Ideal candidates should have at least 10 years in MSAT, specifically...Full time
- Legend Biotech USA is seeking a Global Viral Vector MSAT Lead to provide technical leadership for viral vector manufacturing in Raritan, NJ. The role involves oversight of GMP manufacturing processes, ensuring compliance and reliability. Ideal candidates will have at least...
$160k - $276k
...Director, Global Medical Affairs – Scientific Communications Lead Location: Raritan, New Jersey, United States of America. Job Description... ...reasoning Business requirements analysis Clinical research and regulations Clinical trials operations Communication Developing others...- ...Information Technology (IT), Clinical Research, Rehabilitation Therapy... .... Job Description Title: Lead Clinical Research Associate Location... ...and study tools for site and CRA use • Assistance in formation... ...collection and filing into the Trial Master File Qualifications...
$250k - $280k
...A global biopharmaceutical company is seeking a Global Market Access Director/Senior Director based in New Jersey. The role involves defining and executing pricing and reimbursement strategies while working closely with cross-functional teams. Candidates should have 8...- ...will have over 10 years of experience in technology and product development, along with expertise in PTC Windchill and ThingWorx. The role involves leading cross-functional teams and managing a multi-million-dollar budget to enhance MedTech capabilities. #J-18808-Ljbffr...
- ...seeking a Senior Program Manager, Geo Unit Ops & Compliance in Piscataway Township, New Jersey. This role involves leading compliance for geographic units globally, resolving operational compliance issues, and developing training programs. Candidates should have a Bachelor'...
- ...Regulatory Operations/Affairs Manager to oversee regulatory support activities within External Manufacturing. This role involves managing global market registrations, coordinating quality dossier reviews, and ensuring compliance with regulatory requirements. The ideal...
$250k - $280k
...A global biopharmaceutical company is seeking a Global Market Access Director/Senior Director to lead the US pricing and reimbursement strategy. This hybrid role requires strong engagement with US payers and strategic negotiation skills. Candidates should possess 8-10...$92k - $148.35k
...&D Operations Job Sub Function: Clinical Trial Project Management Job Category:... ...This individual will be responsible for leading one or several clinical trials within the... ...trial management or equivalent is required; global experience preferred Medical device...Local areaImmediate startRemote work- ...149-DePuy Synthes Products Inc. is seeking a Senior Manager in Global Transparency Reporting based in New Brunswick, New Jersey. This... ...programs, and generous time-off policies. Join us to drive compliance initiatives at a leading healthcare company. #J-18808-Ljbffr...
$175k - $300k
...finding treatments and cures. We lead where medicine is going and... ...for the best talent for the Sr. Global Medical Affairs Lead for Lung... ...for leading aspects of the clinical-commercial optimization for EGFR... ...Research and Regulations, Clinical Trials Operations, Communication,...Temporary workLocal areaWorldwide- ManpowerGroup Global, Inc. is seeking a remote Software Labeling Project Manager to coordinate labeling system migrations and deployments in a regulated MedTech setting. Candidates must have strong expertise in Loftware labeling systems and experience in cross-functional...Remote job
- ...include managing vendors, updating program metrics, and establishing effective communication with stakeholders. Join our mission to inspire and impact students and educators globally through effective program management. #J-18808-Ljbffr Spectrum 360 A NJ Non Profit Corp.
$250k - $280k
A global biopharmaceutical company is seeking a Global Market Access Director/Senior Director to lead the US pricing and reimbursement strategy. This hybrid role requires strong engagement with US payers and strategic negotiation skills. Candidates should possess 8-10 years...- Legend Biotech USA, Inc. is seeking a Workday HCM Functional Manager to oversee and optimize the global Core HR module within Workday. This role involves managing configuration, coordinating system enhancements, and supporting biannual releases to drive improvements in...Permanent employmentContract work
- Johnson & Johnson seeks a Manager, TPO Customer Service to drive customer service technology solutions across its global orthopedic organization. The role requires a Bachelor’s degree and 6-8 years in product ownership or IT delivery. Key responsibilities include owning...
$170k - $205k
A leading clinical research organization is seeking an Associate Director of Statistical Programming based in Bridgewater, New Jersey. This role involves managing clinical trial programs, providing oversight to project teams, and ensuring quality deliverables. Candidates...- Colgate-Palmolive in Piscataway, New Jersey is seeking an Engineer, NA SC System to integrate disciplines within the Global and Regional Supply Chain organization. The role focuses on driving process improvements and leveraging digital technologies for better system capabilities...
$124k - $174k
A global consumer products company seeks a Consumer Affairs Global Systems & Ops Manager based in Piscataway, NJ. The successful candidate will enhance consumer experience by managing technology strategies and overseeing operational effectiveness. Applicants should have...- A leading technology organization located in New Brunswick, NJ is seeking a Quality Systems Manager to oversee the Quality Systems and Training within Global External Manufacturing. The ideal candidate will ensure compliance with regulatory requirements, provide day-to-...
- Experis is seeking a Siemens Opcenter MES Project Manager in New Brunswick, New Jersey, to lead the MES deployment on a global scale. You will collaborate with cross-functional teams to ensure seamless transitions in the MedTech manufacturing industry. The ideal candidate...Remote job
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to CRA II: Lead Global Clinical Trials ( ). Be the first to apply!

