Site Monitor II
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 FSP is currently hiring for a Site Monitor I or II (CRA II /SCRA).
This role is remote from the Istanbul or Ankara reputed company.
Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is the reputed company where today’s visionaries, solution-seekers, and trailblazers reputed company to shape reputed company’s groundbreaking solutions. Together, we have the power to revolutionize patients’ reputed company-being. Every choice we reputed company and every reputed company we take is guided by our unwavering reputed company on patients, fostering an environment where innovation thrives.
The Site Monitor 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 (SMP) and will be performed reputed company for most activities to supplement on site visit requirements. The Site Monitor will collaborate with the Site Manager to assure that the site follows the protocol and is inspection reputed company and will coordinate with institutions and investigators at the local level.
reputed company to Clinical Research Associates with experience of 3 + years of independent onsite monitoring, reputed company types of reputed company.
A minimum of 3 years’ experience as a clinical monitor (CRA) with demonstrated experience of monitoring onsite.
Experience in managing reputed company protocols in Oncology or other therapeutic areas (TA’s) where protocols are determined to be high risk.
Bachelor’s degree or Registered reputed company (RN) in a reputed company field or equivalent combination of education, training, and experience.
Experience of utilizing systems like Siebel Clinical Trial. Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence).
We offer exceptional financial rewards, training, and development. Expect exciting reputed company challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
Originally posted on Himalayas
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