Sr Medical Manager PSS

Bengaluru - India

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Summary of Responsibilities:

Responsible for medical review of serious adverse events and adverse events of special interest fromclinical trialsin support of drug safety activities for clients.
When applicable responsible for preparation and medical review of Aggregate Reports required by global regulatory agencies for review of safety information for assigned products when authorized to perform this function on behalf of a client.
When applicable responsible for signal detection and evaluation activities and preparation and submission of Ad Hoc Reports reviewing specific safety issues to the global regulatory agencies for assigned products when authorized to perform this function on behalf of a client.
Participates in training opportunities to advance knowledge of pharmacovigilance as it relates to drug/product development and drug/product marketing utilizing good clinical practice guidelines.
Provides medical/safety expertise to project teams including communicating information regarding drug safety regulations and any changes that have occurred.
Reviews laboratory values adverse events coding dictionaries and data tables listings and figures as needed to identify drug safety issues in collaboration with the project physician.
Assists in the preparation of pharmacovigilance materials for investigator meetings.
Provides pharmacovigilance support to project physicians as appropriate.
Participates in project risk assessment activities.
Assumes responsibility for medical and safety monitoring on assigned projects.

Qualifications (Minimum Required):

MBBS and/or MD with at least 2 years of clinical medicine experience. Experience in Oncology therapy area (Clinical Trial or Post marketing PV) is a must have.

Preferred Qualifications Include:

MD who has completed an accredited residency program or equivalent and is board-eligible or certified with at least 5 years experience with substantial knowledge of drug safety and the global regulations governing pharmacovigilance and patient safety.

Experience (Minimum Required):

At least 5 years of experience working either for a pharmaceutical company health authority or a contract research organization in pharmacovigilance or patient safety.

Physical Demands / Work Environment:

Remote-Based as requested by the line manager.
Work Timings: 2 PM - 11PM IST.

Learn more about our EEO & Accommodations request here.

Required Experience:

Manager

Summary of Responsibilities:Responsible for medical review of serious adverse events and adverse events of special interest fromclinical trialsin support of drug safety activities for clients.When applicable responsible for preparation and medical review of Aggregate Reports required by global regul...

Summary of Responsibilities:

Responsible for medical review of serious adverse events and adverse events of special interest fromclinical trialsin support of drug safety activities for clients.
When applicable responsible for preparation and medical review of Aggregate Reports required by global regulatory agencies for review of safety information for assigned products when authorized to perform this function on behalf of a client.
When applicable responsible for signal detection and evaluation activities and preparation and submission of Ad Hoc Reports reviewing specific safety issues to the global regulatory agencies for assigned products when authorized to perform this function on behalf of a client.
Participates in training opportunities to advance knowledge of pharmacovigilance as it relates to drug/product development and drug/product marketing utilizing good clinical practice guidelines.
Provides medical/safety expertise to project teams including communicating information regarding drug safety regulations and any changes that have occurred.
Reviews laboratory values adverse events coding dictionaries and data tables listings and figures as needed to identify drug safety issues in collaboration with the project physician.
Assists in the preparation of pharmacovigilance materials for investigator meetings.
Provides pharmacovigilance support to project physicians as appropriate.
Participates in project risk assessment activities.
Assumes responsibility for medical and safety monitoring on assigned projects.

Qualifications (Minimum Required):

MBBS and/or MD with at least 2 years of clinical medicine experience. Experience in Oncology therapy area (Clinical Trial or Post marketing PV) is a must have.

Preferred Qualifications Include:

MD who has completed an accredited residency program or equivalent and is board-eligible or certified with at least 5 years experience with substantial knowledge of drug safety and the global regulations governing pharmacovigilance and patient safety.

Experience (Minimum Required):

At least 5 years of experience working either for a pharmaceutical company health authority or a contract research organization in pharmacovigilance or patient safety.

Physical Demands / Work Environment: