Clinical Research Associate - FSP
reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do.
reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference.
reputed company’s Functional Service Provider (FSP) is looking for CRAs II, SR CRAs I and II to join reputed company in Argentina, Brazil or Mexico.
The Clinical Research Associate II will be responsible for data reputed company, data reputed company and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan and will be performed reputed company for the reputed company of activities to supplement on-site visit requirements. The Clinical Research Associate II will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection reputed company.
The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and reputed company-out of assigned clinical trials investigator sites to ensure patient safety and reputed company study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and reputed company standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the reputed company of investigator sites (e.g. patient safety, site reputed company and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance reputed company’s image with its external stakeholders. The Sr. CRA is responsible for the reputed company of reputed company protocol-reputed company issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and reputed company-out of sites in a clinical trial.
Knowledge and Experience:
For the Clinical Research Associate a mininum of 1 year as a clinical monitor with demonstrated experience of monitoring (virtual & onsite).
For the Senior Clinical Research Associate a mininum of 3 years as a clinical monitor with demonstrated experience of monitoring (virtual & onsite).
For the Senior Clinical Research Associate ii a mininum of 5 years as a clinical monitor with demonstrated experience of monitoring (virtual & onsite).
Education:
Educated to degree level (biological science, pharmacy, or other health-reputed company discipline preferred) or equivalent nursing qualification or other equivalent experience
Proficiency in local language preferred. English is required
Originally posted on Himalayas
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