- Actalent (Newark, NJ)
- Job Title: Clinical Trial Specialist Job Description We are seeking a dedicated Clinical Trial Specialist to join our team, focusing on protocol ... role involves collaborating with various departments to initiate and activate new clinical trial protocols, ensuring compliance with regulatory requirements, and… more
- AdventHealth (Orlando, FL)
- …**Postal Code:** 32803 **Job Description:** + Manages the CTMS build to support clinical trial budgets, including invoicing, time and effort tracking, and ... financial reporting. + Coordinates and tracks CTMS builds of the clinical trial protocols to ensure compliance and timely implementation. + Use current Medicare… more
- Astellas Pharma (New York, NY)
- … Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ensure ... trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical… more
- IQVIA (Parsippany, NJ)
- …Management Solutions team. This mainly includes study build activities within the Clinical Trial Management System (CTMS) by troubleshooting issues, ensuring the ... quality of clinical trial day, and addressing any issues in integrating the CTMS into other systems. This role will also participate in operational strategy… more
- Johns Hopkins University (Baltimore, MD)
- …Specialist_** who will provide administrative support for research centers, research review, and clinical trial committees. The Specialist will ensure that ... formula. **Preferred Qualifications** + Bachelor's Degree. + Experience in a clinical research environment. Classified Title: Research Protocol Specialist … more
- ThermoFisher Scientific (Juneau, AK)
- …providing innovative solutions, including regulatory expertise and client interface. As a Clinical Trial Regulatory Affairs Senior Specialist , you'll provide ... Strong understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; expert… more
- Sumitomo Pharma (St. Paul, MN)
- …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
- IQVIA (East China, MI)
- ** Clinical Specialist / Stroke Rater - Chinese Speaking** **Location:** Remote **Hours:** Estimated 2-12 hours per month, flexible **Role Overview** The ... Clinical Specialist supports stroke clinical ...inter-rater reliability. **Key Responsibilities** + Administer stroke-specific scales to trial participants ( **EQ-5D-5L** - interviewer and proxy versions… more
- J&J Family of Companies (Irvine, CA)
- …and reporting to ensure trial validity. The Medical Affairs Clinical Specialist collaborates closely with cross-functional teams to support successful ... and Johnson Neurovascular is recruiting for a **Medical Affairs Clinical Specialist ** located in Irvine, California, USA....company sponsored clinical studies. + Support the clinical trial team to complete studies in… more
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