Responsibilities:

Conduct a full medical assessment of all serious and Non-Serious Cases;

Upgrade a Non-Serious Case to a Serious Case, where applicable, following the medical assessment;

Review and modify the data entered in respect of a Case as necessary and in accordance with applicable SOPs; and

Approve Serious and Non-Serious Cases.

Accenture shall assume the following responsibilities and perform the following activities with regard to Signal Detection:

Participate in Signal Detection meetings, as requested by Client; and

Provide client with line listings and summary tabulations for each Signal Detection

MD/MBBS (board certified) as a minimum, a higher medical speciality is preferred;

A minimum of 2 - 4 years experience in a clinical practice;

A minimum of 1.5 - 3 years experience in pharmaceutical industry (PV, clinical Research, Medical Affairs areas of experience are preferred);

Thorough knowledge of Word and Excel required;

Experience in reviewing data listings and safety reports from clinical trials;

Sound medical knowledge;

Well organized, structured person, with a logic approach to issues raised;

Ability to comprehend and interpret clinical data;

Understanding of complexities of pharmacovigilance is preferred;

Location:Bangalore



For further details please contact:

adarsh.pb@accenture.com

+91 80 40777026