Doctor

ClinSync Clinical Research Pvt Ltd

1. The investigator shall be responsible for the conduct of the trial according to the protocol and the Good Clinical Practices Guidelines, Ethical guidelines and also for compliance as per the undertaking (PIU) and Standard operating procedures.

2. The investigator is responsible for supervising any individual to whom the investigator delegates trial-related duties and functions conducted at the trial site.

3. The investigator is responsible for reviewing, and approving the protocol, prior to the ethics committee approval.

4. During and following trial a subject’s participation in trial, the investigator should ensure that adequate medical care is provided to the participant for any adverse events

5. Protection of the Trial Subject.

• Experience

  1 - 4 Years

• No. of Openings

  02

• Education

  MBBS

• Role

  Principal Investigator

• Industry Type

  Hospitals / Medical / Healthcare Equipments

• Gender

  [ Male / Female ]

• Job Country

  India

• Type of Job

  Full Time

• Work Location Type

  Work from Office