IQVIA Work From Home Job Opportunity
IQVIA Released Job Openings On 25/10/2022.The Company offers commercial, physical, and biological research and development services, as well as value-based analyses, research studies, clinical management analytics, and health outcome optimization services.Application form link provided at the end of post. Eligibility for the Country Clinical Research Lead as follows.
Vacancy Details:
IQVIA Recruiting Bachelor or higher University degree in life sciences, nursing or medical background preferred with 05+ Years Experience for Country Clinical Research Lead Position.Complete Details for the Country Clinical Research Lead as follows.
Important Details :
- Location : England, United Kingdom Remote
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: NA
- Opening date for online Application: 25/10/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Job Description/Skills Required
The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, to support pipeline, in accordance with ICH/GCP, Incyte SOPs, local operating guidelines and local requirements, as applicable. CRL works locally, supporting Associate Director Clinical Operations (ADCO) / Director Clinical Operations (DCO), to ensure corporate/country goals for recruitment and completion of key R&D sponsor deliverables are met.
Responsibilities
• Support ADCO / DCO to:
o Oversee local CRO activities, acting as Single Point of Contact for key and strategic outsourced clinical studies, to ensure corporate and country objectives are reached and potential country issues properly followed-up.
o Collaborate and liaise with Clinical Study Teams and Global Monitoring, for in-house clinical studies conducted within countries ensuring key project milestones and high quality are delivered.
o Partner with local Study Startup Specialist (SSS) or Clinical Research Associates (CRAs) to ensure consistency and accuracy of all core documents for local EC submission, as applicable, for in-house clinical studies (i.e. submission pack, document customization, translations, quality check).
• Support Feasibility process to:
o Carry out top Level feasibilities, to collect key information on competitive clinical studies, marketed and non-marketed drugs, regulatory concerns, Standard of care, etc…
• Build up professional relationship with the investigators and Key Opinion Leaders.
• Liaise with Country, ADCO/DCA and EU CRA Manager for CRAs assignment
• Once trained, support the Global Monitoring team to conduct co-monitoring and CRA assessment visits, when needed and requested
• Supports ADCO / DCO to prepare internal initiatives, meetings and trainings (as required)
• Support the ADCO / DCO to implement local SOPs / WIs, quality/compliance review and initiatives, to ensure inspection readiness
Comments
Post a Comment