- RWJBarnabas Health (New Brunswick, NJ)
- …- $129,204.00 per year Location: New Brunswick, New Brunswick, NJ 07757 Job Title: Clinical Document Specialist Location: Barnabas Health Corp Department: ... Clinical Document SpecialistReq #:0000175148 Category:Revenue Cycle...educational background, skills and professional experience. Job Overview: A clinical documentation specialist (CDS) reviews a patient's… more
- ICON Clinical Research (Basking Ridge, NJ)
- Clinical Study Specialist (Office-based) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an ... us on our mission to shape the future of clinical development. **What you will be doing** + Organizes...informed consent forms, case report forms and facilitates study document reviews per company standard operating procedures + Compiles… more
- Sedgwick (Trenton, NJ)
- …Place to Work(R) Fortune Best Workplaces in Financial Services & Insurance Disability Clinical Specialist **PRIMARY PURPOSE** : Performs standard clinical ... absence from work. **ESSENTIAL FUNCTIONS and RESPONSIBILITIES** + Performs standard clinical reviews of referred medical claims based on client requirements to… more
- Sumitomo Pharma (Trenton, NJ)
- …+ Assist with the entry of Contractual Agreements into an electronic document repository. + Ensure all outsourcing decisions are properly documented, compliant, and ... escalation to senior leadership when appropriate. + Work cross-functionally with clinical teams, Finance and Legal, towards solutions; process, and communication… more
- BriteLife Recovery (Englewood, NJ)
- …clinical information and advocating for appropriate levels of care. The UR Specialist works closely with clinical staff, admissions, medical providers, and ... What you will be doing? The Utilization Review (UR) Specialist is a critical member of the administrative team at Advanced Revenue Solutions and is responsible for… more
- System One (Plainsboro, NJ)
- …quality, performance, regulatory compliance, and patient safety related to managing assigned clinical trial sites and document handling. + Attends and ... Job Title: Retention Specialist Location: Hybrid schedule onsite 3x/week in Plainsboro,...+ Ensures implementation of best possible retention in key clinical trials and works closely in collaboration with Medical… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Summary** The Legal eDiscovery Specialist position will work with eDiscovery and cybersecurity stakeholders to ... with various business functions which requires the Legal eDiscovery Specialist position to possess stellar interpersonal prowess and communication capabilities.… more
- Bristol Myers Squibb (Madison, NJ)
- …data across all cell therapy sites and systems in support of commercial and clinical GNSP operations. The Senior Specialist , Supply Chain Product Data Management ... will identify data owners and engage, define, coordinate, and document key data management processes, along with respective roles and responsibilities, for the… more
- Terumo Medical Corporation (Somerset, NJ)
- SAP GRC and Cloud Security Specialist Date: Dec 4, 2025 Req ID: 5107 Location: Somerset, NJ, US, 08873 Company: Terumo Medical Corporation Department: SAP ... products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part… more
- RWJBarnabas Health (New Brunswick, NJ)
- Cardio Vascular Invasive Specialist , RCIS, or Radiologic TechReq #:0000137970 Category:Radiology / Imaging / Radiation Status:Full-Time Shift:Day Facility:RWJ New ... procedures. Data Management * Participates in data collection in order to document compliance with regulations and measure the quality of patient outcomes. *… more
- Healthfirst (NJ)
- …Assistant Assessments and identify any issues or risk factors that require clinical escalations to a CM//PCM.** + **Initiate and finalize authorization in Trucare ... and update and discontinue authorizations when applicable** + **Handle and accurately document calls to and from members to assist with benefit questions//issues,… more
- Deloitte (Jersey City, NJ)
- …peer review medium to complex changes and test builds/enhancements, new releases etc. and document all outcomes of testing and serve as the support contact for the ... desktop skills including Word, Excel, PowerPoint + Work Experience/Direct Knowledge of clinical area or business area to be supported + Analytical/ Decision Making… more
- Sanofi Group (Morristown, NJ)
- …+ Develop the clinical part of Briefing regulatory documents, Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc ) and answers to ... **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown,...Collaborate with the Patient Safety GSO to detect and document any safety signal + Participates in Advisory Committee… more
- Sanofi Group (Bridgewater, NJ)
- …the limits of what you thought was possible. Ready to get started? The Senior Clinical Research Director (Sr CRD) is noted as the **primary clinical lead for ... + Act as a mentor for other CRDs and Clinical Scientists on a same project/TA + Collaborate with...part of submission dossier for their projects: Common Technical Document for FDA & EMA submission, filing in Japan… more
- Parexel (Trenton, NJ)
- …consensus. + Supervise collection of documentation by Medical Writing Support Coordinator, Document Specialist , and/or Associate Medical Writer for assembly of ... brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD)...and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety… more
- Parexel (Trenton, NJ)
- …client and team informed of project status. + Contribute expertise as a document /cross- document specialist and content historian to analyze proposed program, ... will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as...prepare any type of medical writing deliverable. + Revise document drafts based on the review comments from team… more
- Sanofi Group (Morristown, NJ)
- …you thought was possible. Ready to get started? **Main Responsibilities:** ** Document Development** + Create high-quality regulatory-compliant clinical documents ... or equivalent specialist role + Proven track record leading multiple clinical documentation projects + Expert in clinical documentation preparation **… more
- Deloitte (Jersey City, NJ)
- …environment? As an experienced Epic Break AP Senior Consultant - Project Delivery Specialist you will have the ability to share new ideas and collaborate on ... on 01-Jan-2026 Work you'll do/Responsibilities As a Project Delivery Specialist II (PDS II) at Deloitte, you will work...+ Work command center shifts to investigate during go-live, document , and resolve break-fix tickets. + Conduct and … more
- System One (New Brunswick, NJ)
- …scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority ... high quality technical reports. + Plan and facilitate submission kick-off for clinical regulatory submissions across CTD pipeline assets. + Manage the logistical… more
- ATI Physical Therapy (Trenton, NJ)
- … Clinical Expertise:** We invest in our providers through specialist certifications in ergonomics, early intervention, and occupational health. + **Research ... clinical experience to conduct comprehensive risk and health assessments. + Document all clinical activities thoroughly and efficiently, while actively… more