There are vacancy for CRA I / CRA II / Sr CRA in Jubilant Clinsys.
Job Title : CRA I / CRA II / Sr CRA in Jubilant Clinsys
Company Name : Jubilant Clinsys
Location : NJ / PA /NY / Ohio or NV / AZ, CA or Texas.
Education :Bachelor’s degree, preferably in life sciences
Experience : 2 years field monitoring experience, preferably in Neurology, Psychiatry, Dermatology and CNS.
About Company :
Jubilant Clinsys offers a full range of clinical research services including:
Job Title : CRA I / CRA II / Sr CRA in Jubilant Clinsys
Company Name : Jubilant Clinsys
Location : NJ / PA /NY / Ohio or NV / AZ, CA or Texas.
Education :Bachelor’s degree, preferably in life sciences
Experience : 2 years field monitoring experience, preferably in Neurology, Psychiatry, Dermatology and CNS.
About Company :
Jubilant Clinsys is a contract research organization that provides pharmaceutical, biotechnology and medical device companies with a full range of services in support of Phase I – IV drug and device development. The company is a subsidiary of Jubilant Life Sciences and a fully integrated partner with Jubilant Biosys and Jubilant Chemsys. Founded in 1992, the company operates globally at offices in Bedminster, New Jersey, USA; Raleigh, North Carolina, USA; Ottawa, Ontario; Canada, Noida and Bangalore, India and Dusseldorf, Germany.
Jubilant Clinsys offers a full range of clinical research services including:
- Bioanalytical Services
- Biostatistics
- Clinical Informatics
- Clinical Laboratory
- Clinical Operations
- Clinical Pharmacology/Pathology
- Data Management/EDC
- Drug Safety
- Medical Affairs
- Medical Writing
- Pharmacovigilance
- Project Management
- Quality Assurance
- Regulatory Services
- Willingness to travel up to 80%
- Clinical monitoring and site management activities to ensure compliance with Clinsys’ and/or the Sponsor’s SOPs as well as Good Clinical Practices (GCPs), ICH guidelines and FDA regulations
- ensure subject safety and timely delivery of project
- provide timely monitoring reports in accordance with the Clinical Monitoring and Site Management Plan for assigned trials and will also assist with the development of materials for clinical study conduct
- Must be able to work independently with limited supervision and have the ability to manage time, monthly calendar, expenses and all deadlines per Clinsys policies and procedures.
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