Job Description
Title: Executive, Medical Affairs
Company Name: US FDA Approved Leading Pharmaceuticals Company
Vacancy: --
Age: at most 35 years
Location: Dhaka
Salary: Negotiable
Published: 21 Apr 2024
Education:
∎ MBBS from government recognized institute/ university with BMDC registration.
∎ MBBS from government recognized institute/ university with BMDC registration.
Requirements:
Additional Requirements:
∎ Age at most 35 years
∎ Ability to generate creative ideas and work under pressure.
∎ Collaborative team focus and ability to lead and inspire across departments.
∎ Excellent verbal, written and presentation skills.
∎ Excellent computer skills.
∎ In depth knowledge of event planning and operations.
∎ Ability to generate creative ideas and work under pressure.
∎ Collaborative team focus and ability to lead and inspire across departments.
∎ Excellent verbal, written and presentation skills.
∎ Excellent computer skills.
∎ In depth knowledge of event planning and operations.
Responsibilities & Context:
∎ Organizing and conducting scientific seminars, CME programs and workshops to establish close rapport with the Doctors.
∎ Collecting, compiling, and editing articles for the Organization's Medical Publication.
∎ Writing articles for newsletters.
∎ Response to the Medical information inquiry.
∎ Establish, maintain and update an efficient, comprehensive, robust PV system that may help him/her in disposing his/her obligations of ensuring Risk/Benefit Management of all products throughout their life cycle and PV obligations pertaining to BPL partner companies.
∎ Ensure that reports of all Adverse Event/Serious Adverse Event are recorded and reported according to BPL and Regulatory requirements.
∎ Coordinate and / or liaise with external Regulatory Agencies and / or internal /external stake holders from time to time or as required for disposing his primary responsibility & Pharmacovigilance obligations.
∎ Organizing and conducting scientific seminars, CME programs and workshops to establish close rapport with the Doctors.
∎ Collecting, compiling, and editing articles for the Organization's Medical Publication.
∎ Writing articles for newsletters.
∎ Response to the Medical information inquiry.
∎ Establish, maintain and update an efficient, comprehensive, robust PV system that may help him/her in disposing his/her obligations of ensuring Risk/Benefit Management of all products throughout their life cycle and PV obligations pertaining to BPL partner companies.
∎ Ensure that reports of all Adverse Event/Serious Adverse Event are recorded and reported according to BPL and Regulatory requirements.
∎ Coordinate and / or liaise with external Regulatory Agencies and / or internal /external stake holders from time to time or as required for disposing his primary responsibility & Pharmacovigilance obligations.
Workplace:
∎ Work at office
Employment Status: Full Time
Job Location: Dhaka
Company Information:
∎ US FDA Approved Leading Pharmaceuticals Company
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Application Deadline: 28 Apr 2024
Category: Medical/Pharma
