- Actalent (Newark, NJ)
- Job Title: Clinical Trial Specialist Job Description As a Clinical Trial Specialist , you will coordinate the initiation and activation of new ... clinical trial protocols. This role involves verifying necessary approvals from various boards and committees, preparing study tools, and ensuring that all… more
- Sumitomo Pharma (Trenton, NJ)
- …on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring ... that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and inspections....for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable… more
- IQVIA (Parsippany, NJ)
- ** Clinical Specialist Consultant - Spanish Speaking** **Location:** Remote / Virtual **Hours:** Estimated 10-16 hours per month **Role:** Clinical ... clinical trials. **About the Role** As a Clinical Specialist , you will play a critical...critical role in ensuring the accuracy and consistency of clinical trial assessments. Your responsibilities include reviewing… more
- ICON Clinical Research (Basking Ridge, NJ)
- …or deviations from monitoring plan + Monitors and updates investigator/site status for the trial , and supports with clinical trial registry postings + ... Clinical Study Specialist (Office-based) ICON plc... Clinical Study Specialist (Office-based) ICON plc is a world-leading healthcare...Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study… more
- System One (Plainsboro, NJ)
- Clinical Contracts Specialist Location: REMOTE Comp:...month - highly renewable Must haves: + Experience in Clinical Trial Contracts (CRO or Pharma) + ... Operations Sr. Associates. Essential Functions - Project Support: + Reviews clinical trial protocols and develops investigator cost per patient budgets and site… 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,... trials. + A minimum of 5 years of clinical trial experience within a pharmaceutical, biotechnology,… more
- Deloitte (Princeton, NJ)
- …clients within the Life Sciences & Healthcare sector, utilizing Veeva Vault Clinical Trial Management Systems (CTMS), Regulatory Information Management ( RIM) ... of health. Work you'll do As an Industry Solutions Specialist Leader you will lead the creation of innovative...Suite, and electronic Trial Master File (eTMF) + 6+ years of experience… more
- Parexel (Trenton, NJ)
- …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites...Partners with other Study Team members (eg Clinician, Recruitment Specialist , Clinical Data Scientist) + May act… more
- Merck (Rahway, NJ)
- …viral dynamics, model-based meta-analysis, and other model-based analyses + Perform clinical trial simulations to inform dose selection and go/no-go ... of global regulatory expectations of drug and vaccine development, including clinical trial design, clinical pharmacology, biomarker plans, and model-based… more
- Actalent (Parsippany Troy Hills, NJ)
- Job Title: Regulatory Affairs SpecialistJob Description We are seeking a full-time Clinical Research & Regulatory Affairs Specialist to work remotely for at ... amendments, adverse events, and reportable events, with minimal supervision. The specialist will also handle regulatory documentation for the NCI, organize and… more