Experience: 2 to 4 yrs.
To prepare and update the database of Investigators across India.
Regularly interact with clinical trial sites/SMO and collect the require details.
Conduct the feasibility study based on the Study synopsis/Protocol and gather the details on time.
Compile the data, analyse them and prepare the report in coordination with Medical and Operation team.
Prepare the network of KOLs and interact with them regularly.
Prepare the training material for Operation team.
Must have experience of working as a clinical operation team member in clinical trials dept.
Have broad knowledge and understanding of epidemiological data of various therapeutic areas such as Oncology, Diabetes, Dermatology, Pulmonary, Neurology & Psychiatry etc.
Have experience of conducting feasibility studies and identification of new sites.
Interested candidates can mail their resumes to careers@cliantha.in
Education: M.Pharm, MBBS
Read More
To prepare and update the database of Investigators across India.
Regularly interact with clinical trial sites/SMO and collect the require details.
Conduct the feasibility study based on the Study synopsis/Protocol and gather the details on time.
Compile the data, analyse them and prepare the report in coordination with Medical and Operation team.
Prepare the network of KOLs and interact with them regularly.
Prepare the training material for Operation team.
Must have experience of working as a clinical operation team member in clinical trials dept.
Have broad knowledge and understanding of epidemiological data of various therapeutic areas such as Oncology, Diabetes, Dermatology, Pulmonary, Neurology & Psychiatry etc.
Have experience of conducting feasibility studies and identification of new sites.
Interested candidates can mail their resumes to careers@cliantha.in
Education: M.Pharm, MBBS
Read More
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