Medical Safety Expert Sandoz

Sandoz; India; Presencial; INR 800.000 - 1.500.000; Jornada completa

Descripción de la vacante

Sandoz in India seeks a Drug Safety Specialist responsible for the drug surveillance program, including follow-up, risk assessment, and relatedness to product on adverse reaction reports.

You will provide safety support to clinical development teams, assist in regulatory and clinical document safety input, and mentor junior staff while ensuring compliance with regulations.

Formación

• Experience in safety surveillance for drugs and adverse reaction reports.
• Ability to provide safety input to regulatory and clinical documents.
• Lead training and mentoring of junior team members.
• Act as SME for Medical Operations and safety function.
• Cooperate with Health Authority queries and safety deliverables.

Responsabilidades

• Co-author safety documents and provide safety input to regulatory and clinical documents.
• Monitor safety profile via literature review and case evaluations.
• Support Health Authority queries and regulatory submissions.
• Assist in safety deliverables for new indications.
• Prepare responses to internal and external safety requests.
• Lead SME efforts and mentor junior colleagues.

Conocimientos

Drug safety surveillance

Adverse reaction reports analysis

Safety signal detection

Regulatory compliance

Clinical development safety input

Training and mentoring

English language

Descripción del empleo

Job Description

Job Description Summary

-Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs. Participates in the resolution of any legal liability and complying with governmental regulations. Provides and contributes trending and safety signal detection and risk management assessment for the products’ life cycle. Provides safety support to the clinical development teams.

Job Description

Major accountabilities

• Provides support according to the needs for delivery activities, i.e. co-authoring safety documents and assisting in providing safety input to regulatory and clinical documents, as well as ad hoc Health Authority queries.
• Assist in monitoring the safety profile of products including with activities such as literature review, medical review/evaluation of individual cases or signal detection.
• Perform literature review -Provide support for the preparation of ad hoc Health Authority queries for TAs, also in particular for short term notice requests.
• Perform follow up activities on Health Authority Assessment Reports.
• Assist in providing safety input to Regulatory Affairs and clinical documents.
• Support maintenance and management of local deviations -Assist in evaluating and writing other safety deliverables as assigned -Provide support as needed for new indication submission (regulatory document safety input).
• Prepare responses to internal safety requests and contribution to responses to external safety queries.
• Act as Subject Matter Expert (SME) for Medical Operations/ Medical Function -Lead the training and mentoring of junior team members/colleagues -Distribution of marketing samples (where applicable)

Key performance indicators

• Timeliness and quality of safety analyses, interpretations, and presentations -Compliance with internal and external regulations and procedures -Compliance, consistency and quality of safety deliverables

Minimum Requirements

Work Experience

• People Challenges.
• Managing Crises.
• Functional Breadth.
• Collaborating across boundaries.
• Operations Management and Execution.
• Project Management.

Skills

• Clinical Research.
• Clinical Trials.
• Functional Teams.
• Literature Review.
• Medical Records.
• Process Safety.
• Regulatory Compliance.
• Safety Science.
• Languages :
• English.

Skills Desired

Clinical Research, Clinical Trials, Functional Teams, Literature Review, Medical Records, Process Safety, Regulatory Compliance, Safety Science