Dentist

at  Cliantha Research Ltd

JOB DESCRIPTION

Cliantha Research Inc. is currently seeking a part-time Dentist; who can fulfill its business needs and is looking for better learning and growth opportunities.

ABOUT US

Cliantha Research Inc. is a full service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Tobacco Research, Dermatology, Consumer Research, Research Lab, IVRT, Biometrics, Pharmacovigilance & Medical Services, and Environmental Exposure Chambers (EECs).
With several advanced clinical sites and bio-analytical laboratories in North America and India, Cliantha now has presence in 4 countries along with a strong team of 1000+ professionals. Some of the key regulators, such as the USFDA, EMA, AGES, ANSM, AMPS, MCC South Africa, Health Canada, DCGI, CAP, NABL, Turkey MOH, Thailand MoPH and others have successfully inspected Cliantha across the globe.
Cliantha Research is headquartered in Ahmedabad and has expanded its domestic presence with 5 regional offices & international presence with offices in USA (Florida & New Jersey), Canada (Mississauga, Winnipeg & Scarborough) & Europe (Portugal).

QUALIFICATIONS:

1. Licensed Dentist/ NDEB, DMD
2. Demonstrated knowledge of Quality Standards and regulatory requirements
3. Master’s Degree (preferred), MDS

GENERAL RESPONSIBILITIES:

• Assumes responsibility for relevant trial-related decisions
• Documents the various aspects of the trial
• Discloses conflicts of interest as described in the regulations (as applicable) and ensures protocol compliance
• Demonstrates a thorough understanding of the safety requirements of protocol
• Protects the rights and welfare of subjects
• Endorses changes or corrections to a case report form
• Is thoroughly familiar with the Investigator brochure, use of the investigational product(s), and/or other source information
• Ensures documentation of study-related procedures, processes and events
• Ascertains the reason for a subject’s premature study withdrawal
• Documents adverse experiences per protocol
• Complies with written procedures to document changes to data and/or case report forms and directs the conduct of the clinical trial
• Participate in monitoring visits and audits as appropriate