TMF Lead II - Durham

The TMF Lead II is responsible for the completeness and accuracy of the Trial Master File (TMF) for all sponsored studies.They provide project management principles for all sponsored clinical trials throughout the lifecycle of the trial. · ...

The Contract Specialist plays an important role in driving costings and contracts. · -Adapt global templates of agreements to local use. · -Develop and negotiate clinical site budgets based on Fair Market Value. · -Negotiate agreement language and budget with clinical study sites ...

The Contract Specialist plays an important role in driving the costings and contracts for clinical trials. · ...

The Clinical Trial Administrator (CTA) performs study-related tasks as required by the department.Activities will be conducted in compliance with Company or Sponsor SOPs and regulatory standards and guidelines applicable. · ...

Fortrea is currently seeking a US remote based Clinical Data Strategy & Delivery Lead - FSP to drive and support process development. · This is an (exempt) full-time, home-based position in the USA that will require willingness to work flexible hours as needed to meet business ne ...

IQVIA is seeking a Clinical Research Associate 2 with a minimum of 1.5 years of on-site oncology monitoring experience. · ...

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. · ...

The Clinical Trials Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience and level of contribution which they can make to th ...

Role Overview: As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. · Key Responsibilities:Conduct selection, initiation, monitoring and close-out visits · Collaborate with sites to develop and track recruitmen ...

IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager · to lead and coordinate global and regional clinical trial management activities. · ...

Join our team as a Clinical Research Site Manager where you ll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols regulations and sponsor requirements · Site Monitoring Conduct selection initiation monitoring and close out visits in li ...

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. Must have experience monitoring in oncology solid tumor. · IQVIA Biotech is a full-service CRO p ...

Job Overview: · Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · Essential Functions: · • Perform site moni ...

Job Overview · Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements. · Essential Functions · Site Monitoring: Conduct selection, initia ...

Fortrea is currently seeking a US remote based Sr Specialist, Clinical Data Strategy & Operations (CDSO) – FSP to drive and support process development evaluation and implementations projects that are led by the CDSO Process Excellence and Delivery team or co-led with the Global ...

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) or Cardiovascular clinical trials. Phase 1 experience is a plus · Job Overview · Perform monitoring and site management work to ensure that sites are conducting ...

IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) or Cardiovascular clinical trials. Phase 1 experience is a plus · ...

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · ...

+Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, · applicable regulations and guidelines, and sponsor requirements. · +Ensure copies/originals (as required) site documents a ...

Fortrea is currently seeking a US remote based Sr Specialist to drive process development evaluation and implementations projects led by CDSO Process Excellence Delivery team. · ...