IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
IQVIA is looking for experienced CRAs willing to discover how a true partnership between the CRO and sponsor works! Join us and benefit from its advantages:
- Working with one of the TOP 5 sponsors globally
- The chance to work on cutting edge medicines right at the forefront of drug development
- ‘Fit for Purpose monitoring’ - reduced travel due to using risk based monitoring.
- International proyects and enviroment
- Focus on quality vs quantity!
- Flexible conditions and an attractive remuneration package
Responsibilities:
- Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans.
- Administer protocol and related study training to assigned sites and establish regular lines of communication.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations – escalating quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
Required Knowledge and skills:
- In depth knowledge and skill in applying applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- In depth therapeutic and protocol knowledge as provided in company training
- Strong written and verbal communication skills including good command of English language
- Excellent organizational and problem-solving skills
- Effective time management skills
Minimum Required Education & Experience :
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- +1 year of monitoring experience as an independent CRA
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
IQVIA is looking for experienced CRAs willing to discover how a true partnership between the CRO and sponsor works! Join us and benefit from its advantages:
- Working with one of the TOP 5 sponsors globally
- The chance to work on cutting edge medicines right at the forefront of drug development
- ‘Fit for Purpose monitoring’ - reduced travel due to using risk based monitoring.
- International proyects and enviroment
- Focus on quality vs quantity!
- Flexible conditions and an attractive remuneration package
Responsibilities:
- Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans.
- Administer protocol and related study training to assigned sites and establish regular lines of communication.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations – escalating quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
Required Knowledge and skills:
- In depth knowledge and skill in applying applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- In depth therapeutic and protocol knowledge as provided in company training
- Strong written and verbal communication skills including good command of English language
- Excellent organizational and problem-solving skills
- Effective time management skills
Minimum Required Education & Experience :
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- +1 year of monitoring experience as an independent CRA
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.
Qué requisitos cumples
Criterios proporcionados por el anunciante del empleo
Criterios proporcionados por el anunciante del empleo
Aptitudes
-
Investigación
-
Inglés
-
Viajes
-
Requisitos regulatorios
-
Investigación clínica
-
Ensayos clínicos
-
Redacción de consultas
- Investigación
- Inglés
- Viajes
- Requisitos regulatorios
- Investigación clínica
- Ensayos clínicos
- Redacción de consultas
Nivel educativo
-
Bachelor's Degree
- Bachelor's Degree
Detalles del empleo
Nivel de experiencia
Algo de responsabilidad
Algo de responsabilidad
Sector
- Industria farmacéutica
- Industria farmacéutica
Tipo de empleo
Jornada completa
Jornada completa
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