Who are we?
Teva is a global pharmaceutical leader and the world\'s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world\'s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we\'ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
To ensure all assigned studies follows SOPs, GCP and applicable regulations
To do all regulatory/ethics submission as per timelines and to ensure regulatory documents are available, complete and current
In coordination with the project manager and/or medical monitor, perform study site selection visits. Participate in/conduct investigator\'s meeting and site initiation visits
To perform regular monitoring visits to site
To verify the case report forms and source data according to the monitoring plan
To ensure site level metrics (i.e. 100% IP accountability, 100% informed consent documentation etc.) are tracked and communicated as appropriate
Conduct site close out and assure appropriate archival of controlled documents
Resolve issues as they affect clinical plan timelines and quality to ensure achievement of goals and objectives at the site level
Work in liaison with the finance department in the organization and administration of financial payments to the investigators or relevant local institutions
To ensure the compliance to ICH-GCP guidelines, local & international regulations (Ex. DCGI, FDA) and applicable SOP
Qualifications
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