Job Description:- Coordinates the conduct of clinical trials from pre-study planning through successful completion of all patient visits and documentation; directly involved in patient care. Works under the supervision of the Principal Investigator and Medical Director.
ROLES AND RESPONSIBILITIES
* Maintains a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, tests, procedures, laboratory information, and drug accountability requirements.
* Responsible for completion of all study documentation forms, including case report forms and other study specific documents
* Coordinates and conducts patient care visits and assures all procedures are conducted in compliance with the clinical protocol
* Interacts with Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed; alerts Principal Investigator of serious adverse events
* Interacts with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process
* Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols
* Conducts clinical research in compliance with all applicable regulations and Radiant SOPs
OVERVIEW OF QUALIFICATIONS:(1-4YRS EXP)
Bachelor degree in health care profession preferred
CONTACT:-
Sagacia Soft Technologies Services Pvt Ltd
ssahu@sagacia.in
ROLES AND RESPONSIBILITIES
* Maintains a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, tests, procedures, laboratory information, and drug accountability requirements.
* Responsible for completion of all study documentation forms, including case report forms and other study specific documents
* Coordinates and conducts patient care visits and assures all procedures are conducted in compliance with the clinical protocol
* Interacts with Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed; alerts Principal Investigator of serious adverse events
* Interacts with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process
* Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols
* Conducts clinical research in compliance with all applicable regulations and Radiant SOPs
OVERVIEW OF QUALIFICATIONS:(1-4YRS EXP)
Bachelor degree in health care profession preferred
CONTACT:-
Sagacia Soft Technologies Services Pvt Ltd
ssahu@sagacia.in
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