- 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
- 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
- Kelly Services (Irvine, CA)
- …study team in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, ... Clinical FSP is currently seeking a Associate Clinical Research Specialist for a long-term engagement... clinical study team in the development of clinical trial documents (eg study protocol, informed… 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
- Abbott (Abbott Park, IL)
- …colleagues serve people in more than 160 countries. **Job Title** Sr. EP Field Clinical Specialist - Central/Western US **Working at Abbott** At Abbott, you can ... are seeking an experienced, high caliber Senior EP Field Clinical Specialist . This position will be primarily...therapy area. + Serve as a technology, protocol and clinical trial procedure expert and resource Abbott… more
- Edwards Lifesciences (St. Paul, MN)
- …exam results for consistency with case report form, and determining if clinical trial /study subject documentation is within parameters of study hypothesis, ... as well as monitoring clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. + Providing… more
- Edwards Lifesciences (Kansas City, KS)
- …exam results for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters of study hypothesis, ... as well as to monitor clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Develop and deliver… more
- Veterans Affairs, Veterans Health Administration (Tulsa, OK)
- …Oklahoma VA Healthcare System is hiring 2 Medical Records Technicians ( Clinical Documentation Improvement Specialist (CDIS-Inpatient) located in Tulsa, OK. ... will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness...for all positions above the journey level; however, for clinical documentation improvement specialist assignments, a … more
- University of Pennsylvania (Philadelphia, PA)
- …entry and query resolution; and assisting with all aspects of complex clinical trial visits, including recruitment/enrollment, visit scheduling and patient ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist A Job Profile...tasks to help support the conduct of industry sponsored clinical research/ trial protocols in the Penn FTD… more
- Actalent (Altamonte Springs, FL)
- …Application/CTMS Specialist plays a pivotal role in the management of clinical trial budgets and protocols. This position involves expertise in Medicare ... Job Title: Clinical Trials Applications/CTMS Specialist Job Description...well as patient and study status reporting within the Clinical Trial Management System (CTMS). The role… more
- Cedars-Sinai (Los Angeles, CA)
- …and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all federal ... NOT available for this position at this time. The Clinical Research Specialist II provides clinical...coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. + Ensures compliance… more
- Houston Methodist (Houston, TX)
- …Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research ... Performs clinical research support functions as assigned by the clinical trial manager including but not limited to informed consent for non-interventional… more
- Actalent (Alameda, CA)
- …packaging projects, including oversight of CMO scheduling, production of labels, and packaging of clinical trial supplies. + Review clinical trial ... Job Title: Clinical Supply SpecialistJob Description The Clinical Supply Specialist plays a pivotal role...ensure compliance with US and international regulations. + Represent clinical supplies function at clinical trial… more
- Actalent (North Chicago, IL)
- …verify patient activity for each agreement, and independently investigate and resolve clinical trial vendor or site payment disputes. Responsibilities + Ensure ... Job Title: Clinical Contract Documentation Specialist IIIJob Description...resolve issues independently or with minimal oversight. + Coordinate clinical trial payments to ensure timely processing,… more
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