- 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
- Terumo Neuro (Aliso Viejo, CA)
- **12870BR** **Title:** Sr Specialist , Clinical Trial Quality Assurance **Job Description:** Provide support to all aspects of the Clinical Quality ... Hiring Ordinance, and San Francisco Fair Chance Ordinance. **External-Facing Title:** Sr Specialist , Clinical Trial Quality Assurance **Posting Country:** US… more
- Actalent (Durham, NC)
- Job Title: TMF Specialist Job Description To maintain continuity and compliance across ongoing medical device trials, we are seeking a TMF Specialist to provide ... dedicated support and ensure the integrity of trial documentation. Responsibilities * Maintain and oversee the Trial Master File (TMF) for active medical device… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more
- Astellas Pharma (San Diego, CA)
- … 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
- Boehringer Ingelheim (Ridgefield, CT)
- … clinical programs across Therapeutic areas, ie, Clinical Associates (CAs), Clinical Trial Operations Specialist (CTOS), Regulatory Start Up ... for forecasting and providing oversight of resources supporting US Clinical Trial Managers (CTMs)and managing the Site...Specialist (RSUS), Informed Consent Specialist (ICS) Site Activation Manager (SAM), Establishes standards. This… 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
- Georgetown Univerisity (Washington, DC)
- …Trials Unit will work with and assist the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial Manager by entering data into ... will work with and assist the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial Manager by interacting with the clinical … more